Professional Documents
Culture Documents
VE6_VE8_COVER.FM
GE Healthcare
• Voluson E6 / Voluson E8 / Voluson E10 with Software version EC300, 15.x.x (BT15)
• Voluson E6 / Voluson E8 / Voluson E10 with Software version EC310, 16.x.x (BT16)
• Voluson E6 / Voluson E8 / Voluson E10 with Software version EC320, 17.x.x (BT17)
• Voluson E6 / Voluson E8 / Voluson E10 with Software version EC330, 18.x.x (BT18)
0123
Revision History
Introduction
This chapter describes important issues related to safely servicing the Voluson E-
Series (Voluson E6, Voluson E8 and/or Voluson E10) ultrasound system. The
service provider must read and understand all the information presented in this
manual before installing or servicing this system.
Note Under consideration of general maintenance requirements a minimum lifetime of 7 years for the
equipment and 5 years for the probes may be expected. To maintain the safety and performance of
the ultrasound system, a regular check (once per year) by authorized personnel is recommended.
Damage in transportation
All packages should be closely examined at time of delivery. If damage is apparent write “Damage In
Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by a GE
representative or hospital receiving agent. Whether noted or concealed, damage MUST be reported to the
carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and
containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an
inspection is not requested within this 14 day period.
GE employees should use the global complaint recording tool to report service documentation issues. These
issues will then be in the internal problem reporting tool and communicated to the writer.
Danger
Dangerous voltages, capable of causing death are present in this system. Use extreme caution when
handling, testing and adjusting.
Warning
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling
pad, to reduce the risk of injury.
Trademarks
All products and their name brands are trademarks of their respective holders.
Copyrights
© 2014 - 2017 by General Electric Company Inc. All Rights Reserved.
Note The Voluson E6 is a “feature-reduced” version of the Voluson E8 ultrasound system. That means not all
options are available on the Voluson E6 (marked with an asterisk * in sections of this manual).
The service manual is divided into 10 chapters. In the beginning of the manual, before chapter 1, you will find
the revision overview and the Table of Contents (TOC).
The language policy for GE’s service documentation, the omission & errors and the legal information are
included in the beginning of this chapter (chapter 1).
Chapter 4 – Functional Checks Contains functional checks that are recommended as part of the
installation, or as required during servicing and periodic maintenance.
Chapter 5 – Components and Functions Contains block diagrams and functional explanations of the electronics.
(Theory)
Chapter 8 – Replacement Procedures Provides disassembly procedures and reassembly procedures for all
Field Replaceable Units (FRU) and Customer Replaceable Units (CRU).
The screen graphics and illustrations in this Service Manual are for illustrative purposes only and may be
slightly different from what is displayed on the screen or device.
Voluson E6 Systems
Voluson E8 Systems
The operator manuals should be fully read and understood before operating the Voluson E-Series system
and also kept near the system for quick reference.
The online versions of the operator manual is available via the Help function (F1 key) on Voluson E-Series
control console.
The translated online user manuals are available on a CD ROM delivered with the system. They are also
available on OnBase and/or the Common Documentation Library (CDL) for downloading.
MODEL DESIGNATIONS
This manual covers the Voluson E-Series ultrasound systems listed in Models covered by this Manual.
ICONS
Pictures, or icons, are used wherever they reinforce the printed message. The icons, labels and conventions
used on the product and in the service information are described in this chapter.
SAFETY PRECAUTION MESSAGES
Various levels of safety precaution messages may be found on the equipment and in the service information.
The different levels of concern are identified by a flag word that precedes the precautionary message.
Known or potential hazards to personnel are labeled in one of following ways:
• Danger
• Warning
• Caution
Important information will usually be preceded by the exclamation point (!) contained within a triangle, as
seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be used to
make you aware of specific types of hazards that could cause harm. Even if a symbol isn't used in this
manual, it is included for your reference.
Danger
Indicates the presence of a hazard that will cause severe personal injury or death if the instructions are
ignored.
Warning
Indicates the presence of a hazard that can cause severe personal injury and property damage if instructions
are ignored.
Caution
Indicates the presence of a hazard that will or can cause minor personal injury and property damage if
instructions are ignored. Equipment damage possible.
Electric Hazard
Indicates the risk of injury from electric hazards.
Bio Hazard
Indicates the risk of disease transmission or infections.
Explosion Hazard
Indicates the risk of injury from explosion hazards.
Moving Hazard
Indicates the risk of injury from moving or tipping hazards.
Mechanical Hazard
Indicates the risk of injury from mechanical/pinch hazards.
Non-ionizing Hazard
Indicates the risk of injury from non-ionizing radiation.
Operating LED
Indicates the risk of injury from light beams entering the eye. Do not stare into the light beam of the LED.
This icon is used when options or features are specific for BT-Software versions.
This icon is used for special hints, or tips that may facilitate servicing a Voluson E-Series system.
Note Notes are used to provide important information about an item or a procedure.
Be sure to read the notes; the Information contained in a note can often save you time or effort.
Table 1-5 Standard icons that indicates that a special procedure is to be used
Avoid Static Tag and Lock Wear Eye Wear Hand Wear Foot
Electricity Out Protection Protection Protection
The following table describes the purpose and location of labels, safety icons and other important information
provided on the equipment.
Note For more detailed description of all symbols and labels used in combination with this Voluson E-Series
ultrasound system, refer to Chapter 2 in the Basic User Manual.
Device Listing /
Laboratory logo or labels denoting conformance with industry
Certification rear side of the system
safety standards such as UL or IEC.
Labels
CE Conformity mark according to Medical Device Directive 93/42/ Identification and Rating Plate
EEC. 0123: Identification number of notified body TÜV Süd
Product Service. (rear side of the system / on plug of each probe)
"DANGER -
The system is not designed for use with flammable anesthetic
Risk of explosion Indicated in the Service Manual.
gases.
used in ..."
This precaution is intended to prevent injury that may result if one Used in the Service and User Manual which
person attempt to move the system considerable distances or on should be adjacent to equipment at all times for
an incline due to the weight of the system. quick reference.
Pushing prohibited.
Do not lean on the system. Tipping danger. various
Take special care when moving the system.
Loading prohibited.
Do not put any items on this shelf. Danger of breaking. at top cover of the system
Also items might be crushed when lowering the user interface.
Pinch point
Watch your hands and fingers when adjusting the monitor. Keep rear side of the Monitor
hands clear of openings.
This symbol indicates that in the United States of America, federal Identification and Rating Plate
law restricts this device to sale by or on the order of a physician. (rear side of the system)
"Mains OFF" Indicates the power off position of the mains power rear of system at mains switch
switch. (on power supply RSP)
"On/Off” or “Standby"
CAUTION: System shutdown using this button DOES NOT ON/OFF Standby button on control console
disconnect the Voluson E-Series from mains voltage!
"Mains ON" Indicates the power on position of the mains power rear of system at mains switch
switch. (on power supply RSP)
"Protective Earth" Indicates the protective earth (grounding) rear of system at mains switch
terminal. (on power supply RSP)
"Equipotential" Indicates the terminal to be used for connecting rear of system at mains switch
equipotential conductors when interconnecting (grounding) with
other equipment. (on power supply RSP)
Every system has a unique marking for identification, the Unique Identification and Rating Plate
Device Identification (UDI) Label. The UDI label consists of a (rear side of the system / on plug of each probe)
series of (alpha-) numeric characters and barcode which uniquely
identify the Voluson E-Series system as a medical device Upgraded systems
manufactured by General Electric. adjacent to the Rating Plate
The Common Mark of Products Circulation certifies that the Identification and Rating Plate
products bearing this mark, passed all conformity assessment
(approval) procedures. (rear side of the system)
1.5.1 Introduction
The following safety precautions must be observed during all phases of operation, service and repair of this
equipment. Failure to comply with these precautions or with specific warnings elsewhere in this manual,
violates safety standards of design, manufacture and intended use of the equipment.
Danger
Dangerous voltages, capable of causing death are present in this system. Use extreme caution when
handling, testing and adjusting.
Warning
Do not operate the system in an explosive atmosphere. Operation of any electrical equipment in such an
environment constitutes a definite safety hazard.
Warning
Because of the limited access to cabinets and equipment in the field, placing people in awkward positions,
GE has limited the lifting weight for one person in the field to 16 KG (35 LBS). Anything over 16 KG (35 LBS)
requires 2 people.
Warning
If the covers are removed from an operating Voluson E-Series, some metal surfaces may be warm enough
to pose a potential heat hazard if touched, even while in shutdown mode.
Warning
Do not substitute parts or modify the system. Because of the danger of introducing additional hazards, ONLY
install GE Healthcare Austria GmbH & Co OG approved parts. DO NOT perform any unauthorized
modification of the system.
Warning
Use extreme caution as long as the Voluson E-Series is un-stable, not resting on all four caster wheels.
Warning
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling
pad, to reduce the risk of injury.
Warning
Beware of possible sharp edges on all mechanical parts. If sharp edges are encountered, the appropriate
PPE should be used to reduce the risk of injury.
Warning
Wear all PPE including gloves as indicated in the chemical Material Safety Data Sheet (MSDS).
Caution
The Voluson E-Series systems weighs 150 kg or more, depending on installed peripherals, (330 lbs., or
more) when ready for use.
Be careful when moving the system. Two people are required when moving the Voluson E-Series on inclines
or lifting more than 16 kg (35 lbs).
• Always lower and center the control console (UI) to its minimum height and lock it in its parking
(locked) position.
• Secure the monitor for transport: Lock the monitor arm and flap down the LCD monitor.
• Use the rear handle to move the system.
• Remove all obstacles.
• Move the system slowly and carefully.
• Avoid collisions with walls or door frames.
• Always place the system on horizontal ground and engage the caster brakes.
• Do not move the system when the brakes are engaged.
• Move the system forward or backward when going up or down inclines. Do not move the system
sideways or diagonally.
Failure to follow the precautions could result in injury, uncontrolled motion and costly damage.
Warning
Ultrasound systems and probes are highly sensitive medical instruments that can easily be damaged by
improper handling. Use care when handling and protect from damage also when not in use. Do not use a
damaged or defective ultrasound system or probe. Failure to follow these precautions can result in serious
injury and system damage.
Warning
Never use a probe that has fallen to the floor. Even if it looks OK, it may be damaged.
Note Special care should be taken when transporting the system in a vehicle:
• Eject any DVD/CD from the drive.
• Place the probes in their carrying cases.
• DO NOT use the control console as an anchor point.
• Secure the system with straps in an upright position and lock the caster wheels (brake).
• Ensure that the Voluson E-Series system is firmly secured while inside the vehicle.
• Drive cautiously to prevent vibration damage.
Warning
Connecting a Voluson E-Series system to the wrong voltage level will most likely destroy it.
1.5.4.2 Probes
All probes for Voluson E-Series systems are designed and manufactured to provide trouble-free, reliable
service. To ensure this, correct handling of probes is important and the following points should be noted:
• Do not drop a probe or strike it against a hard surface, as this may damage the probe elements,
acoustic lens, or housing.
• Inspect the probe prior to each use for damage or degradation to the housing, cable strain relief, lens,
seal, connector pins and locking mechanism.
• Do not use a cracked or damaged probe. In this event, call your field service representative
immediately to obtain a replacement.
• Avoid pulling, pinching or kinking the probe cable, since a damaged cable may compromise the
electrical safety of the probe.
• Never immerse the probe connector or adapter into any liquid.
• The system has more than one type of probe port. Use the appropriate probe port designed for the
probe you are connecting.
Note For detailed information on handling probes, refer to the Voluson E-Series Basic User Manual and the care
card supplied with the probe.
Caution
Power supplies for additional equipment MUST comply with IEC 60601-1.
Caution
Do not attempt to use different peripherals and accessories (brand and model; connected via USB port)
other than approved and provided by GE Healthcare Austria GmbH & Co OG! The Voluson E-Series
ultrasound system is an extremely sensitive and complex medical system. Any unauthorized peripherals may
cause system failure or damage.
Voluson E-Series systems are equipped with an isolation transformer to provide the required separation from
AC mains for both, the system and the auxiliary devices. One AC mains power outlet is located at the power
supply. It is used for connecting the threefold/fourfold splitter whose outlets are led to the shelves, intend for
auxiliary devices (e.g., printers).
The IEC60601 standard provides a guideline for safely interconnecting medical devices in systems.
“Equipment connected to the analog or digital interface must comply with the respective IEC standards (e.g.
IEC60950 for data processing equipment and IEC60601-1 for medical equipment).
Everybody who connects additional equipment to the signal input portion or signal output portion configures
a medical system, and is therefore responsible that the system complies with the requirements of the system
standard IEC60601.
1. The medical device may be connected to a single IEC XXX device (protection class I) placed in a room
which is not medically used.
2. If the device is to be connected in a medically-used room the following rule applies:
- IEC XXX compliant devices (protection class I) may be connected with an additional safety
measure.
- IEC 60601 compliant devices may be connected as such.
For all situations 1 and 2, the additional device shall be installed outside the typical patient environment.
Possible additional safety measures are additional protective earth connection between the 2 devices, or a
safety isolation mains transformer for the other device.
Special care has to be taken, if the device is connected to computer network (e.g., Ethernet), because other
devices could be connected without any control. There could be a potential difference between the protective
earth and any line of the computer network including the shield.
In this case the only way to operate the system safely is to use an isolated signal link with minimum air
clearance and creepage distance of the isolation device in agreement with IEC60601 incl. national
deviations. For computer networks there are media converters available which convert the electrical to
optical signals. Please consider that this converter has to comply with IEC xxx standards* and is battery
operated or connected to the isolation mains output of the Voluson E-Series ultrasound system.
* IEC xxx stands for standards such as:
• IEC60601 for medical devices
• IEC60950 for information technology equipment etc.
Note The system integrator (any person connecting the medical device to other devices) is responsible that
connections are safe. If in doubt, consult the technical service department or your local representative.
Caution
The leakage current of the entire system including any / all auxiliary equipment must not exceed the limit
values as per EN60601-1-1 (IEC60601-1-1) respectively other valid national or international standards. All
equipment must comply with CSA, IEC or other relevant requirements.
Caution
Please observe that some printers may not be medical devices! If Bluetooth-, Line- or Laser Printers are no
medical devices, they have to be located outside of the typical patient environment. Examples for typical
patient environments can be found in standard IEC 60601 (see illustrations below).
Caution
Auxiliary equipment must only be connected with the special main outlet provided for the electrical safety of
the system.
Caution
Auxiliary equipment with direct main connection requires galvanic separation of the signal and/or control
leads.
Note Always observe the instructions given in the manual of the peripheral/auxiliary device.
For hardware installation procedures see: Chapter 3 – Setup Instructions
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
Note All peripherals mounted on the Voluson E-Series system chassis must be firmly secured in position.
The Voluson E-Series ultrasound system comes equipped with product labels and icons. These labels and
icons represent pertinent information regarding the operation of the system.
Note For description of all symbols and labels used in combination with this Voluson E-Series ultrasound system,
refer to Section 1.4.3 on page 1-16 and Chapter 2 in the Basic User Manual of your system.
The layout of the Identification and Rating Plate depends on BT-version and/or date of manufacture.
4 Power Consumption nominal 10 TUEV NRTL Certification mark 16 UDI label (barcode and characters)
19 Part number
Warnings, such as the examples below, precede potentially dangerous procedures throughout this manual.
Instructions contained in the warnings must be followed.
Danger
Dangerous voltages, capable of causing death are present in this system. Use extreme caution when
handling, testing and adjusting.
Warning
If the covers are removed from an operating Voluson E-Series, some metal surfaces may be warm enough
to pose a potential heat hazard if touched, even while in shutdown mode.
Warning
Do not operate the system in an explosive atmosphere. Operation of any electrical equipment in such an
environment constitutes a definite safety hazard.
Warning
Do not substitute parts or modify the system. Because of the danger of introducing additional hazards, ONLY
install GE Healthcare Austria GmbH & Co OG approved parts. DO NOT perform any unauthorized
modification of the system.
Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are
in total control of the AC power plug at all times during the service process.
To apply Lockout/Tagout (LOTO):
1. Plan and prepare for shutdown.
2. Shutdown the equipment.
3. Isolate the equipment.
4. Apply Lockout/Tagout Devices.
5. Control all stored and residual energy.
6. Verify isolation.
All potentially hazardous stored or residual energy is relieved.
Warning
Energy Control and Power Lockout for Voluson E-Series:
When servicing parts of the system where there is exposure to voltage greater than 30 Volts:
1. Follow LOTO (Lockout/Tagout) procedures.
2. Turn off the breaker.
3. Unplug the Voluson E-Series system.
4. Maintain control of the Voluson E-Series system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.
When returning or shipping the Voluson E-Series system in the original packaging:
• system must be lowered to its minimum height with monitor flapped down
• the control console has to be centered and locked in “unextended” position
Note For control console positioning see Section 6.3 on page 6-4 .
Equipment being returned must be clean and free of blood and other infectious substances.
GE policy states that body fluids must be properly removed from any part or equipment prior to shipment. GE
employees, as well as customers, are responsible for ensuring that parts/equipment have been properly
decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids
be taken or shipped from a clinic or site (for example, body coils or and ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the people
who will receive or open this package.
Note The US Department of Transportation (DOT) has ruled that “items what were saturated and/or dripping with
human blood that are now caked with dried blood; or which were used or intended for use in patient care”
are “regulated medical waste” for transportation purpose and must be transported as a hazardous material.
Note The user/service staff should dispose of all the waste properly, per federal, state, and local waste disposal
regulations.
The Voluson E-Series system is not meant to be used for long-term storage of patient data or images. The
user is responsible for the data on the system and a regular backup is highly recommended.
If the system is sent for repair, please ensure that any patient information is backed up and erased from the
system before shipping. It is always possible during system failure and repair to lose patient data. GE is not
responsible for the loss of this data.
If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes, GE will
ascertain agreement from the customer. Patient information shall only be transferred by approved service
processes, tools and devices restricting access, protecting or encrypting data where required, and providing
traceability in the form of paper or electronic documents at each stage of the procedure while maintaining
compliance with cross-border restrictions of patient information transfers.
1.6.2 Compliance
The Voluson E-Series system conforms to all applicable conducted and radiated emission limits and to
immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line
transient requirements as mentioned in IEC60601-1-2.
Note For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are in good
condition, installed tightly without skew or stress. Proper installation following all comments noted in this
service manual is required in order to achieve full EMC performance.
Warning: DO NOT touch any boards with integrated circuits prior to taking necessary ESD precautions.
1. When installing boards, ESD may cause damage to a board. ALWAYS connect yourself, via an arm-
wrist strap, to the advised ESD connection point located on the rear of the system (to the right of the
power connector).
2. Follow general guidelines for handling of electrostatic sensitive equipment.
If the system does not work as indicated in this service manual or in the Basic User Manual, or if you require
additional assistance, please contact the local distributor or appropriate support resource, as listed below.
Note Prepare vital system information (see: Section 7.1 on page 7-2 ) before you call:
• System Type
• System Serial number (also visible on label on back of the system)
• Application Software version
• Backup version
• additional information about installed software
Site Preparation
This chapter provides the information required to plan and prepare for the
installation of a Voluson E-Series system. Included are descriptions of the facility
and electrical needs to be met by the purchaser.
Operating Temperature Operating Humidity Heat Dissipation Storage Temperature Storage Humidity
Caution
If the system has been in storage, has been transported or is very cold or hot, do not turn on its power until it
has had a chance to acclimate to its operating environment. (see: Section 3.1.2 "Installation Warnings" on
page 3-2 ).
2.1.1.1 Cooling
The cooling requirement for a Voluson E-Series system is 2730 BTU/hour. This figure does not include
cooling needed for lights, people, or other equipment in the room.
Note Each person in the room places an additional 300 BTU/hr demand on the cooling system.
2.1.1.2 Lighting
Bright light is needed for system installation, updates and repairs. However, operator and patient comfort
may be optimized if the room light is subdued and indirect. Therefore a combination lighting system (dim/
bright) is recommended. Keep in mind that lighting controls and dimmers can be a source of EMI which
could degrade image quality. These controls should be selected to minimize possible interference.
Note GE Healthcare Austria GmbH & Co OG requires a dedicated power and ground for the proper operation of
its Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the
system.
The Ultrasound will function on voltages from 100-240 Volts and 50 or 60 Hz. However, if using 220 volt
power in North America, then a center tapped power source is required.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size
ground wire from the distribution panel to the ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size
ground wire from the distribution panel to the ultrasound outlet.
Note Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's
incoming power source to the ultrasound system is only a conduit.
AC mains power outlets (AUX) for auxiliary devices and peripherals are co-switched by the systems mains
switch. Output voltage for AUX: 115V
Caution
The maximum power consumption of equipment (inclusive color LCD monitor) connected to these outlets
must not exceed 200VA!
Ultrasound systems are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic
fields, and transients in the air or wiring. They also generate EMI. The Voluson E-Series system complies
with limits as stated on the EMC label. However, there is no guarantee that interference will not occur in a
particular installation.
Note Possible EMI sources should be identified before the system is installed.
Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. Sources of
EMI include the following:
• medical lasers
• scanners
• cauterizing guns
• computers
• monitors
• fans
• gel warmers
• microwave oven
• light dimmers
• mobile phones
• in-house wireless phones (DECT phones)
• wireless computer keyboard and mouse
• air conditioning system
• High Frequency (HF) surgery equipment
• general AC/DC adapters
The presence of a broadcast station or broadcast van may also cause interference.
Be aware of Radio Keep the system at least 5 meters (15 feet) away from other EMI sources. Special shielding may be
Frequency sources. required to eliminate interference problems caused by high frequency, high powered radio or video
broadcast signals.
Ground the system. Poor grounding is the most likely reason a system will have noisy images. Check grounding of the
power cord and power outlet.
Assemble all screws, Radio After you finish repairing or updating the system, assemble all covers and tighten all screws. Any
Frequency gaskets, covers cable with an external connection requires a magnet wrap at each end. Install all covers. Loose or
and cores. missing covers or Radio Frequency gaskets allow radio frequencies to interfere with the ultrasound
signals.
Replace broken Radio If more than 20% or a pair of the fingers on an Radio Frequency gasket are broken, replace the
Frequency gaskets. gasket. Do not turn ON the system until any loose metallic part is removed.
Do not place labels where Never place a label where Radio Frequency gaskets meet the system. Otherwise, the gap created
Radio Frequency gaskets will permit Radio Frequency leakage. In case a label has been found in such a position, move it to
touch metal. another more suitable location.
Use GE- specified harnesses The interconnect cables are grounded and require ferrite beads and other shielding. Also, cable
and peripherals. length, material, and routing are all important; do not change from what is specified.
Take care with cellular Cellular phones may transmit a 5 V/m signal; that could causes image artifacts.
phones.
Properly route peripheral Do not allow cables to lie across the top of the card rack or hang out of the peripheral bays. Loop the
cables. excess length for peripheral cables inside the peripheral bays. Attach the monitor cables to the
frame.
Site preparation takes time. Begin site preparation checks as soon as possible. If possible, six weeks before
delivery, to allow enough time to make any changes.
Warning
Have two people available to deliver and unpack the Voluson E-Series ultrasound system.
Attempts to move the system considerable distances (or on an incline) by one person alone, could result in
personal injury and/or damage to the system.
Table 2-4 physical dimensions and weight (without monitor and peripherals)
1533 mm / 60.4 inch * 582 mm / 22.9 inch 1168 mm / 46.0 inch * 150 kg / 330 lbs.
1333 mm / 52.5 inch ** 968 mm / 38.1 inch **
* maximum at “normal” monitor position (control console is lifted and moved forwards to the maximum)
** minimum at “normal” monitor position (no control console lifted or forwards movement)
The work and materials needed to prepare the site is the responsibility of the purchaser. Delay, confusion,
and waste of manpower can be avoided by completing pre-installation work before delivery.
Use the Pre-installation checklist (provided in Table 2-5) to verify that all needed steps have been taken.
Action Yes No
Notify installation team of the existence of any variances from the basic installation.
Make sure system and probes have been subject to acclimation period.
EMI precautions have been taken and all possible sources of interference have been removed.
If a network is used, IP address has been set for the system and a dedicated network outlet is available.
Note All electrical installations that are preliminary to the positioning of the equipment at the site prepared for the
equipment must be performed by licensed electrical contractors. Other connections between pieces of
electrical equipment, calibrations, and testing must also be performed by qualified personnel. The products
involved (and the accompanying electrical installations) are highly sophisticated and special engineering
competence is required. All electrical work on these products must comply with the requirements of
applicable electrical codes. The purchaser of GE equipment must only utilize qualified personnel to perform
electrical servicing on the equipment.
The desire to use a non–listed or customer provided product or to place an approved product further from the
system than the interface kit allows presents challenges to the installation team. To avoid delays during
installation, such variances should be made known to the individuals or group performing the installation at
the earliest possible date (preferably prior to the purchase).
The ultrasound suite must be clean prior to delivery of the machine. Carpet is not recommended because it
collects dust and creates static. Potential sources of EMI (electromagnetic interference) should also be
investigated before delivery. Dirt, static, and EMI can negatively impact system reliability.
• dedicated single branch power outlet of adequate amperage (see: Table 2-2 on page 2-2 ), meeting all
local and national codes, which is located less than 2.5 m (8.2 ft. / 98.4 in.) from the system's proposed
location.; see Section 2.1.2 "Electrical Requirements" on page 2-2 .
• door opening is at least 76 cm (2.5 ft./ 30 in.) wide
• proposed location for the system is at least 0.5 m (1.6 ft. / 19.6 in.) from the wall for cooling
• power outlet and place for any external peripheral are within 2 m (6.5 ft. / 78.7 in.) of each other with
peripheral within 1 m of the system to connect cables.
• power outlets for other medical equipment
• power outlets for test equipment within 1 m (3.2 ft. / 39.4 in.) of system
• clean and protected space to store probes (in their cases or on a rack)
• material to safely clean probes (done with a plastic container, never metal)
Note The Voluson E-Series has four outlets inside. One for the monitor and three for on board peripherals.
In case of network option:
• An active network outlet in the vicinity of the ultrasound system.
• A network cable of appropriate length (regular Pin-to-Pin network cable).
• An IT administrator who will assist in configuring the system to work with your local network. A fixed IP
address is required. Refer to the form provided in Figure 3-65 for network details that are required.
Note All relevant preliminary network port installations at the prepared site must be performed by authorized
contractors. The purchaser of GE equipment must utilize only qualified personnel to perform servicing on the
equipment.
3 counter top, sink with hot and cold water, supplies storage 10 external peripherals
• Voluson E-Series Details: DICOM network details for the Voluson E-Series system, including the
host name, local port, IP address, AE title and net mask.
• Routing Information: IP addresses for default gateway and other routers in use at site.
• DICOM Application Details of DICOM devices in use at the site, including the DICOM host
Information: name, AE title, DICOM port number and IP addresses.
Note For further details refer to the Voluson E-Series Basic User Manual.
1 DICOM is the registered trademark of the National Electrical Manufacturers Association for its standards publications relating to digital communications
of medical information.
Setup Instructions
Once the site has been prepared, the average installation time required is shown in Table 3-1 below.
Installing the system / options / printers 0.5 to 1.5 hours depends on required configuration
Caution
Since the Voluson E-Series weighs approximately 150 kg (330 lbs.) without peripherals, two people are
required to unpack it.
Warning
There are no operator serviceable components. To prevent shock, do not remove any covers or panels.
Should problems or malfunctions occur, unplug the power cord.
Only qualified service personnel should carry out servicing and troubleshooting.
Caution
• Do not pull or lift the system with the front handle of the user interface (control console).
• Always use a strap to lift the system. Do not grasp the metal sheet with your hands.
• Move the system forward or backward when going up or down inclines. Do not move the system
sideways or diagonally.
Caution
Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the
system to be damaged.
hrs 8 6 4 2 0 0 0 0 0 0 0 2 4 6 8 10 12 14 16 18 20
Caution
The system should not be moved with the control console (UI) extended. Move the control console to it's
centered and locked position for transport.
Caution
Monitor mounting mechanism may break if not properly supported (e.g., with packing foam) during
transportation.
Danger
When using any test instrument that is capable of opening the AC ground line (i.e., meter's ground switch is
OPEN), DO NOT touch the system!
Caution
To prevent electrical shock, connect the system to a properly grounded power outlet. DO NOT use a three to
two prong adapter. This defeats safety grounding.
Caution
When connecting the optional PE (potential equalization) and/or the optional additional GND (ground cable)
it is mandatory to also use the Power Filter (H48701EL).
Caution
Two people should unpack the system because of its weight. Two people are required whenever a part
weighing 16kg (35 lb.) or more must be lifted.
Caution:
Do not wear the ESD wrist strap when you work on live circuits and more than 30 V peak is present.
Caution
If the system is very cold or hot, do NOT turn on its power until it has had sufficient time to acclimate to its
operating environment.
Caution
Transport only with forklift or stacker truck. During transport pay attention to the point of gravity (“tilt and
drop” indicator)!
Warning
Have two people available to deliver and unpack the Voluson E-Series ultrasound system.
Attempts to move the system considerable distances (or on an incline) by one person alone, could result in
personal injury and/or damage to the system.
Voluson E-Series incl. peripherals 1369 mm / 54 inch 780 mm / 30.7 inch 1086 mm / 42.8 inch 190 kg / 419 lbs.
and accessories
* Weight is approximate and will vary depending upon the supplied peripherals
Note The device must only be transported in the original packaging cardboard!
It is recommended to keep and store the shipping cardboard and all other packing materials (including the
support foams, anti-static plastic cover, etc.), in case the system has to be moved to a different location.
Unpack the system such a way that packaging can be reused. For warranty purposes, storage of the above
is required for one year from date of purchase.
Note If the shipping cardboard is damaged, please inform the GE Healthcare Austria GmbH & Co OG sales
representative immediately.
Unpacking procedure
Unpack the Voluson E-Series ultrasound system and its (optional) peripherals and accessories according to
the provided unpacking instruction.
1. After unpacking, it is important to verify that all items ordered by the customer have been received.
Compare all items listed on the packing slip (delivery note) with those received.
Note It is recommended to keep and store the shipping cardboard and all other packing materials (including the
support foams, anti-static plastic cover, etc.), in case the system has to be moved to a different location.
Unpack the system such a way that packaging can be reused. For warranty purposes, storage of the above
is required for one year from date of purchase.
2. Visually inspect the system components using the following checklist.
1 Rating Plate Enter Serial Number: _________________________ (printed on rating plate, see: Figure 1-1 on page 1-23 )
2 System Verify that the Voluson E-Series system is switched OFF and unplugged. Clean the system.
3 Control Physically inspect the control console for missing or damaged items. After switching on the system, verify
Console the proper illumination of all the control console buttons.
4 Probes Check all probes for wear and tear on the lens, cable, and connector. Look for bent or damaged pins on
the connector and in the connector socket on the system. Verify that the EMI fingers around the probe
connector socket housing are intact. Check the probe locking mechanism and probe switch.
5 LCD Display Clean the LCD display by gently wiping with a dry, soft, lint-free non-abrasive folded cloth. Inspect the
monitor for scratches and raster burn.
6 Fans Verify that the system's cooling fans and peripheral fans are operating.
7 Rear Panel Check the rear panel connectors for bent pins, loose connections and loose or missing hardware. Screw
all the cable connectors tightly to the connector sockets on the panel. Verify that the labeling is in good
condition.
8 Covers Check that all screws are tightly secured in place, that there are no dents or scratches and that no internal
parts are exposed.
9 Peripherals Check and clean the peripherals in accordance with the manufacturer's directions. To prevent EMI or
system overheating, dress the peripheral cables inside the peripheral cover.
10 Power Cord Check the power cord for cuts, loose hardware, tire marks, exposed insulation, or any deterioration. Verify
continuity. Replace the power cord, as required.
Note Report any items that are missing, back-ordered, or damaged, to your GE Healthcare Austria GmbH & Co
OG sales representative. The contact address is shown in "Contact Information" on page 1-26 .
This system has been designed to minimize the effects of Electo-Magnetic Interference (EMI). Many of the
covers, shields, and screws are provided primarily to protect the system from image artifacts caused by this
interference. For this reason, it is imperative that all covers and hardware are installed and secured before
the system is put into operation.
Ensure that the system is protected from electromagnetic interference (EMI), as follows:
• Operate the system at least 15 feet away from equipment that emits strong electromagnetic radiation.
• Operate the system in an area enclosed by walls, floors and ceilings comprised of wood, plaster or
concrete, which help prevent EMI.
• Shield the system when operating it in the vicinity of radio broadcast equipment, if necessary.
• Do not operate mobile phones or other EMI emitting devices in the ultrasound room.
• Verify that all EMI rules listed are followed.
The Voluson E-Series system is approved for use in hospitals, clinics and other environmentally qualified
facilities, in terms of the prevention of radio wave interference. Operation of the ultrasound system in an
inappropriate environment can cause electronic interference to radios and television sets situated near the
medical equipment.
For further details and EMI Prevention/Abatement refer to Section 2.1.3 "EMI Limitations" on page 2-3 .
Caution
Prior to connecting the Voluson E-Series system to a power source, verify compliance with all electrical and
safety requirements. Check the power cord to verify that it is intact and of hospital-grade. Products equipped
with a power source (wall outlet) plug should be connected to the fixed power socket that has a protective
grounding conductor. Never use an adapter or converter to connect with a power source plug (for example, a
three-prong to two-prong converter).
Warning
The system's power must be supplied from a separate, properly rated outlet to avoid risk of fire. Refer to
Section 2.1.2.1 "Voluson Power Requirements Voluson E-Series" on page 2-2 for rating information. The
power cord should not, under any circumstances, be altered to a configuration rated less than that specified
for the current.
Note Use only the power cords, cables and plugs provided by or designated by GE Healthcare Austria GmbH &
Co OG to connect the system to the power source.
Caution
Whenever disconnecting the Voluson E-Series system from the electrical outlet, always observe the safety
precautions. First unplug the main power cable from the wall outlet socket, then from the system itself.
Remove by pulling on the cable connector - Do not pull on the cable.
1 circuit breaker
2 fuses (2x T10A H/250V)
3 connector for main power cable
Note When AC power is applied to the system, the ON/OFF standby button on the control console illuminates
amber, indicating that the system (including the Back-end Processor) is in standby mode.
5. Hold down the ON/OFF standby button (see: Figure 3-3 below) on the control console for ~3 seconds.
Note The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the ON/OFF
standby button. The power switch of any attached printer(s) needs to be in ON position before starting the
system. However, be aware some auxiliary equipment may switch itself to standby mode (e.g., Color video
printer) and must therefore be switched on separately.
When the ON/OFF standby button on the control console is pressed, the system (including the Back-
end Processor) starts and the operating system is loaded which then leads to activate the application
software.
The system automatically performs an initialization sequence which includes the following:
- Loading the operating system.
- Running a quick diagnostic check of the system.
- Detecting connected probes
6. The software initiates and sets up the FrontEnd electronics and the rest of the system (incl. clicking
sound of relays on RTF board).
7. The keyboard backlight is lit.
8. As soon as the software has been loaded, the 2D screen is displayed on the monitor.
Note After turning off a system, wait at least 10 seconds before turning it on again. The system may not be able to
boot if power is recycled too quickly.
1. If not already in read mode, freeze the image.
2. Press the ON/OFF Standby button on the control console. Following dialog appears.
Note A full shutdown is also performed when pressing the ON/OFF standby button on the control console twice.
Note The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the ON/OFF
standby button. So the auxiliary equipment need not to be switched ON/OFF separately.
Warning
Disconnection of the main power cable is necessary!
5. After complete power down, unscrew the 2 screws and remove the pull-out protection to disconnect the
main power cable from the system or unplug it from the AC wall outlet socket.
1 circuit breaker
2 fuses (2x T10A H/250V)
3 connector for main power cable
Caution
Do not disconnect a probe while running (Live Scan “Write” mode)! A software error may occur. In this case
switch the system OFF (perform a reset).
Note When the probe is connected, it is automatically activated. Once connected, probes can be selected for
different applications.
Connect a probe to one of the three rightmost probe receptacle as follows:
1. Inspect the probe and probe socket to verify that it is free of debris.
2. Ensure that the probe locking lever is at horizontal position.
3. Insert the connector on the receptacle guide pin until it touches the receptacle mating surface.
4. Twist the probe locking lever clockwise (to vertical position) to lock it in place.
5. Open the side door, lay the cable into the intended cable holder and close the door.
6. Carefully position the probe cord so that it is free to move and is not resting on the floor.
Caution
• Do not bend the probe cable acutely. Fault conditions can result in electric shock hazard.
• Do not touch the surface of probe connectors which are exposed when the probe is removed.
• Do not touch the patient when connecting or disconnecting a probe.
Note Prior to connecting or disconnecting a probe, freeze the image. It is not necessary to turn OFF power to
connect or disconnect a probe.
Note Always observe the instructions given in the manual of the peripheral/auxiliary device.
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
Caution
Please observe that some printers may not be medical devices! If Bluetooth-, Line- or Laser Printers are no
medical devices, they have to be located outside of the typical patient environment. Examples for typical
patient environments can be found in standard IEC 60601 (see illustrations below).
Note For more detailed Safety Considerations when connecting auxiliary devices to the Voluson E-Series system,
please review: Section 1.5.5 "Auxiliary Devices Safety" on page 1-21 .
Note The OLED Monitor is only available for BT17 (EC320) and BT18 (EC330) Voluson E10 systems. Usually it
comes pre-installed with the system.
Note The B&W printer should be connected to USB port C on the RTB Distribution Board Bottom.
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
2 The UP-D898MD features a legacy mode driver mode. In this mode the printer identifies itself as UP-D897 via the USB interface. This enables
the use of the printer with the driver of UP-D897. Through this feature the new medical printer UP-D898MD can be used to easily replace an
existing UP-D897 unit in the field.
Note The Color printer should be connected to USB port D on the RTB Distribution Board Bottom.
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
Caution
Please observe that the complete Printer Assembly has to be located outside of the patient environment
(according to IEC 60601-1).
Caution
The printer being used may not be a medical device. The (Bluetooth) Printer Set and the Power Supply is
also not a medical device. The equipment meets the requirements of the EN 60950 Standard.
Note It does not matter, whether an Ethernet crossover cable or a patch cable (straight through cable) is used.
The Network Color Laser Printer automatically reconfigures signals to yield expected results.
Note The Network Color Laser printer MUST NOT be installed by the user! For installation please contact your
local distributor or GE service representative.
Figure 3-13 Connection Scheme - Color Laser Printer (directly via network cable)
Figure 3-14 Connection Scheme - Color Laser Printer (within Network Environment)
Figure 3-15 Connection Scheme - Color Laser Printer (Wi-Fi Direct Communication)
Caution
Please observe that the complete Printer Assembly has to be located outside of the patient environment
(according to IEC 60601-1).
Caution
The printer being used may not be a medical device. The (Bluetooth) Printer Set and the Power Supply is
also not a medical device. The equipment meets the requirements of the EN 60950 Standard.
Note Please use the proper Bluetooth Printer Connection set; see: Section 9.10.1 "Printers" on page 9-37 .
Figure 3-16 Connection Scheme - DeskJet Color Printer (via Bluetooth Adapter)
Note If a DeskJet printer (e.g., HP Officejet 100) is connected directly via an USB-cable, use the AC mains power
outlet provided by the Voluson E-Series system (auxiliary output). This ensures medical grade separation
from AC mains.
Figure 3-17 Connection Scheme - DeskJet Color Printer (directly via USB cable)
b. Insert the SIM card (see images below), fix it with the mounted clips and return the upper cover.
Note Since the Voluson E-Series does not enable browser access, the service provider needs to enable the
Internet access on the SIM card before installation in the Cellular Modem. Please ensure from the service
provider, that there is no browser registration necessary when using the SIM card.
3. Connect the Cellular Modem according to connection scheme, see: Figure 3-20 on page 3-27 .
4. Power ON/Boot up the Voluson E-Series system as described in Section 3.4.1 on page 3-9 .
5. After physical connection of the Cellular Modem to the Voluson E-Series system, perform Modem
Configuration as described in Section 3.13.3 "How to Setup the Cellular Modem" on page 3-64 .
6. Click the signal strength icon in the status bar and select Connect for connection to the service
provider.
7. If it is desired to send E-mails, perform configuration as described in Section 3.13.4 on page 3-66 .
8. If it is desired to use also MMS, adjust settings as described in Section 3.13.5 on page 3-67 .
9. Assign the Modem to a remote key (P1, P2, P3, P4, P5 and/or P6) as described in Section 3.6.6
"Remote Control Selection" on page 3-41 and adjust the Email settings.
10. Individually enter Patient's Email address and Phone number in the PID screen and adjust Email
and/or MMS options as described in Section 3.13.6 on page 3-68 .
Note The Cellular Modem should be connected to the USB port B on the RTB Distribution Board Bottom.
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
Note Connection is always the same (no differences between PC-Motherboard version of the Voluson E-Series
system).
1. Turn ON the power of the system and wait till the system has booted.
2. Plug the Wireless Network adapter into an accessible USB port of the Voluson E-Series. All software
drivers are pre-installed for the designated Wireless Network adapter only.
The Wireless Network Adapter can be connected to any accessible USB port.
Note Connection is always the same (no differences between PC-Motherboard version of the Voluson E-Series
system).
Note After physical connection of the WLAN adapter to the Voluson E-Series system, follow the procedure
described in Section 3.13.2 "Wireless Network Configuration" on page 3-59 .
Caution
A Secondary "Patient" Monitor MUST NEVER be connected to the Voluson E-Series systems mains supply
directly! Always connect it to an appropriate Isolation Transformer (see Section 9.10.3 on page 9-42 ).
Caution
The secondary monitor is the only item to be connected to the isolation transformer.
Note A Secondary Monitor is NOT intended for diagnostic use. It is an additional device used to allow the patient
to watch the proceedings.
Note Take your time to think about the best position of the monitor in your facilities. Patients should be able to
view the monitor easily and without having to bend or turn around.
Note Connection is always the same (no differences between PC-Motherboard version of the Voluson E-Series
system).
The Footswitch should be directly connected to any accessible USB-port on the Voluson E-Series (e.g., on
rear of the system).
Note Connection is always the same (no differences between PC-Motherboard version of the Voluson E-Series
system).
After physical connection, adjust the Footswitch as described in Section 3.7.1.8 on page 3-45 .
The Barcode Scanner should be directly connected to any accessible USB-port on the Voluson E-Series
(e.g., next to DVD drive).
Note Connection is always the same (no differences between PC-Motherboard version of the Voluson E-Series
system).
Note Connection is always the same (no differences between PC-Motherboard version of the Voluson E-Series
system).
Note Before connecting an USB device, please read Section 3.5.15 "General Remarks when using external USB-
Devices" on page 3-35 .
An USB Flash Memory Stick may be connected to an accessible USB port of the Voluson E-Series system
(e.g., on back of control console).
An external USB Flash Memory Stick can be connected once the system is powered ON, or after shutdown.
The Voluson E-Series, Windows detects the device and automatically installs a driver. During this process
several dialogs may pop up, starting with the „Found New Hardware” dialog.
Note Memory drives or sticks may be sensitive to EMC interference. This may affect system performance and/or
image quality.
Note Before disconnecting an external USB-device (e.g., USB Stick), the system has to be informed about the
removal of the device! For this purpose press the Eject key on the keyboard.
For further details see Section 3.5.15.2 "External USB-Devices - Disconnection" on page 3-35 .
Note Before connecting an USB device, please read Section 3.5.15 "General Remarks when using external USB-
Devices" on page 3-35 .
An external HDD may be connected to an accessible USB port of the Voluson E-Series system (e.g., on
back of control console).
An external USB Hard Disk Drive can be connected once the system is powered ON, or after shutdown. The
Voluson E-Series, Windows detects the device and automatically installs a driver. During this process
several dialogs may pop up, starting with the „Found New Hardware” dialog.
Note Memory drives or sticks may be sensitive to EMC interference. This may affect system performance and/or
image quality.
Note Before disconnecting an external USB-device (e.g., USB Stick), the system has to be informed about the
removal of the device! For this purpose press the Eject key on the keyboard.
For further details see Section 3.5.15.2 "External USB-Devices - Disconnection" on page 3-35 .
Caution
Do not connect or disconnect any external USB-devices to or from the system while scanning a patient! The
appearing dialogs could distract you from the scan!
Note If an external drive was not recognized automatically after connecting it, click Rescan Drive.
Note When connecting external USB devices, be sure to execute Safety Directions found in the Voluson E-Series
Basic User Manual.
Before an external USB-device (e.g., USB-memory stick) can be disconnected, the system has to be informed about the
removal of the device! For this purpose press the Eject key on the keyboard.
Caution
Unplugging or ejecting USB devices without first stopping them can cause the system to crash and possibly
result in loss of valuable data.
By pressing the Eject key on the keyboard, a dialog window (see: Figure 3-26 below) is displayed. The
“Connect USB and Network Drives” window shows all USB and Network drives connected to the system.
Using this dialog, the USB-devices can be stopped before they are physically disconnected.
To stop the external device, select it and then click the Stop Device button.
Confirm the "‘Stop Device" dialog with OK and Close the "Connect USB and Network Drives" window.
Note The Network Color Laser printer and the Bluetooth printer connection set MUST NOT be installed by the
user! For installation please contact your local distributor or GE service representative.
If a DeskJet printer (e.g., HP Officejet 100) is connected directly via an USB-cable, use the AC mains power
outlet provided by the Voluson E-Series system (auxiliary output). This ensures medical grade separation
from AC mains.
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
Note Settings for paper size must match with the used paper (large/small) and also the right color ink cartridge
has to be used. Otherwise you will get an error message at printing.
3. Select the Graphics page. From the "Color Adjust" pull-down menu select:
4. Color Balance: Cyan = 0, Magenta = 0, Yellow = 0
9. Save the adjusted printer settings with Apply and OK. Close window and exit System Setup.
10. Assign the printer to the remote keys P1, P2, P3, P4, P5 and/or P6; see Section 3.6.6 "Remote Control
Selection" on page 3-41 .
To assign an auxiliary device (e.g., printer) to the remote keys P1, P2, P3, P4, P5 and/or P6:
1. Press the Utilities key on the control console.
2. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
3. On the right side of the screen select Connectivity and then click the Button Configuration tab.
1a Configure buttons
1b Select Printer
1c Recorder Control
1. Overview tab:
a. Configure “Remote” Buttons: Select the desired remote control button.
b. Select Printer: Check mark and select the desired Printer for the remote control button.
c. Recorder Control: Check mark this item to use the selected P? key for Recorder Control.
d. Check mark "Use P? key to send Email", and adjust Settings.
Note Optionally the Printer Remote Control can be done by the Foot switch; see Figure 3-28 on page 3-37 .
2. Detailed Setup tab:
a. If it is desired, check mark "Use Report Printer for Reports"
Note The selected Report Printer is usually used for printing reports and images from the Archive.
3.7.1 Setup
Please observe that the displayed screens may slightly differ from images shown in this manual. The
availability of some functions or features depend on the BT-version of your Voluson E-Series system.
• General: Date, Time, Clinic Name, (EUM) Language, Screen saver, etc.
• Authentication: access setting (password protection) to authentication functions
• Details: Doppler 2D Refresh, Zoom options, Menu Brightness, Trackball Speed, etc.
• Annotation: adjustment of different Annotation presets (e.g. Home position, etc.)
• Clipboard: adjustment of Clipboard display and functions
• Patient Info Display: Drop Down Management, Title Bar Settings, Capitalize Letter in Patient Names, etc.
• Scan Assistant: Scan Assistant List/Item Settings, etc.
• Service: enter the password to get access to the Service Tools functions
• System Info: shows which Software/Hardware version is installed in the system
• Options: shows which options are installed in the system. For information on configuring software options
refer to: Section 8.7 on page 8-16 .
• Disk Encryption: enables an encryption to secure all Patient Data, Patient Images and corresponding
measurements
• Whitelisting: prevents the system from installing unwanted software
• Peripherals: Video Norm selection, Foot switch assignment, Add Printer, Edit Printer settings, etc.
• Device Setup: to set up all DICOM, Archive and Network configuration nodes (e.g, TCP/IP, WLAN, EMAIL,
etc.)
• Button Configuration: adjust assignment of Remote keys P1, P2, P3, ... (e.g, Printer selection)
• Drives: USB and Network drives: stop devices, map network drive, erase CD
• System Configuration: Save/Load Scan Settings (Small Backup), Save/Load/Delete Full System
Configuration
• Image Archive: Save/Load Image Archive
• Presets: to save User Folders/Presets and 3D/4D Presets, Logo display, etc.
• Global Parameters: adjustment of different parameters for specific or all applications
• Measure & Calc: shows all settings, which are used for generic measurements as well as calculations in
different applications
• Application Parameters: to adjust Status on Freeze for different modes, Manual Trace method, Calculation
Ratio, etc.
• Global Parameters: to select cursor type and size, font size and color of measure results, position of results
for different modes, etc.
• Report: adjustment and setup of Report display
• Result Window: adjustment of Result and OB Graph display
• Button Configuration: adjust assignment of buttons
• SonoAVC: adjustment of follicle parameters
Note For further details refer to the Voluson E-Series Basic User Manual.
Note In general operations are done with the trackball and the trackball keys (mouse emulation).
upper / lower trackball key (upper trackball key = right mouse button):
no function in system desktop
Note If the eDOC DVD is not inserted, a message to insert the DVD appears.
3. Click the button to activate a sub dialog window to enter date, time and time zone.
4. Select the “Date Format” (only one can be active).
5. Select the “Time Format” (only one can be active).
6. Close the Service page with Save&Exit.
Note After changing the language the Voluson E-Series has to reboot.
Entering a password is no more required at systems with software version EC330 (BT18).
Note A valid password must be at least 6 characters long and has a maximum length of 80 characters. The
password must contain at least 2 non-letter characters, 0...9 or !@#$%^*().
d. Select a Group the user belong to.
e. Confirm with OK to save User Login Authentication.
4. Close the Service page with Save&Exit and restart the system.
The system login window appears as soon as the system is started or a current user logs off. The correct
User Name and Password has to be entered to login. If the correct password/user name combination is
entered, it is also possible to change the password. The Emergency button enables emergency mode with
restricted access.
Note For further details refer to the Voluson E-Series Basic User Manual.
Caution
Without the Encryption Password or Recovery Key it will not be possible to access the Ultrasound device
including emergency mode, scanning, patient information, images, or local archive. GE has no access to this
information or the ability to undo encryption in the event that the Encryption Password and Recovery Key are
lost. The security and safety of the Encryption Password and Recovery Key is solely the user's responsibility.
Note Disk Encryption is an option and might not be available in all countries. If the option is not set, the tab Disk
Encryption is not available in System Setup - Administration.
Content in this section
3.7.1.13.1 Disk Encryption Workflow - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-47
3.7.1.13.2 Unlock an encrypted Disk - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-47
3.7.1.13.3 Decrypt Disk - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-48
3. Start Encryption.
a. Set unlock password and Retype password.
Note The entered password is not visible and has a minimum of 8 characters.
b. Click Create unlock keys.
Identifier and Recovery key as well as an USB unlock key is automatically created by the system.
c. Save recovery key to an external or network device.
d. Choose connected printer from the pull down-menu and click Print recovery key.
e. If desired, click the Save to USB button to save the USB unlock key to a connected USB device.
f. Click the Start encryption button.
Note The process of enabling encryption of the patient data will take a considerable amount of time (one to
several hours).
g. Confirm the dialogs with Yes and OK to start encryption.
A progress bar is displayed during disk encryption process.
Note The system should not be used while encryption process in ongoing.
If the USB device with unlock key is connected to your Voluson E-Series, the system is automatically
unlocked during boot up.
Note Security of patient data on the system will be reduced when encryption is turned off. Decryption will take a
considerable amount of time (one to several hours).
5. Confirm the dialogs with Yes and OK to start encryption.
A progress bar is displayed during decryption process.
Note The system should not be used while decryption process in ongoing.
Note The entered password is not visible and has a minimum of 8 characters.
4. Click Activate.
5. Close the Service page with Save&Exit and restart the system.
Caution
The maximum power consumption of equipment (inclusive color LCD monitor) connected to these outlets
must not exceed 200VA!
UP-D898MD
Color Deskjet Printer Hewlett Packard (HP) HP Officejet 100 USB-Port or Table 9-10
Bluetooth
Color Laser Printer (Network) Hewlett Packard (HP) HP LaserJet M451 USB-Port Table 9-10
HP LaserJet M452dn
USB Flash Memory device SanDisk Cruzer Micro USB-Port Table 9-11
Gigabit Network Isolator Baaske Medical MI 1005 Medical Isolator USB-Port Table 9-11
A6210
SMX1200XLHG
4 -
32" Secondary Patient Monitor (USA NEC MultiSync V323-2 HDMI / VGA -
and EU)
32" Secondary Patient Monitor (US SONY KDL-32EX523 HDMI / VGA obsolete
version)
It might be possible that some probes, options or features are NOT available
• in some countries.
• at the time of release of this Service Manual.
3 Network Table 3-9 GES30: DICOM input/output, twisted pair RJ-45 10/100 megabit/s
GES35: DICOM input/output, twisted pair RJ-45 10/100/1000 megabit/s
6 S-Video OUT Table 3-12 S-Video OUT connector, PAL/NTSC (depending on system setup)
Figure 3-42 RTH6x => "white" USB2.0 ports / RTH50 => "blue" USB3.0 ports
Figure 3-43 External I/O connectors - on the left/right side of the Monitor
1
USB Table 3-11 USB 3.0 port
2
10 TMDS Clock+
5, 6, 7, 8, 10 GND GND
1 ETHER TD Ethernet RD +
2 ETHER TD Ethernet RD -
3 ETHER RD Ethernet TD +
6 ETHER RD Ethernet TD -
others NC no connection
Pin No Description
2, 3, 7, 10, 15 12V
1, 5, 8, 9, 1116 GND
6 / 14 USB 1- / USB 1+
Video specifications may be needed to be able to connect laser cameras or other devices to the Voluson E-
Series system.
DVI-D/VGA-connector:
• visible resolution ... 1280 x 1024
• screen refresh rate ... 60Hz
S-Video connector:
• Type: separate Video (Y/C)
• Video modes: PAL (50Hz), NTSC (60Hz)
Table below shows maximum permitted cable length of external cables, according to IEC60601-1-2.
PE cable 10 m unshielded
Note For further details refer to the Voluson E-Series Basic User Manual.
This section describes communication and connection options between the Voluson E-Series ultrasound
system and other devices in the hospital information system.
The following scenarios are covered:
• stand-alone Voluson E-Series system; see Section 3.12.1.3 on page 3-57 .
• Voluson E-Series and one or several PC workstations - with Software 4D View installed - within a
“Sneaker Net” environment. (“Sneaker Net” means that you use a DVD/CD to move data because no
network is available); see Section 3.12.1.4 on page 3-57 .
• Voluson E-Series and DICOM server in a network; see Section 3.12.1.5 on page 3-57 .
Note For further details refer to the Voluson E-Series Basic User Manual.
Note To avoid loss of essential data, it is highly recommended to export/backup patient data as well as
measurements at least once a month.
Physical Connection:
No network connection needed.
Note For further details refer to the Voluson E-Series Basic User Manual.
Note To avoid loss of essential data, it is highly recommended to export/backup patient data as well as
measurements at least once a month.
Physical Connection:
No network connection needed.
Note If a Peer-to-Peer Network is connected to the hospital's network, you may connect the Voluson E-Series to
the Peer-to-Peer Network.
Note For further details refer to the Voluson E-Series Basic User Manual.
Note Following information must be provided by the customer or hospital engineer before you can start: Station
name, AE Title, IP address and Port Number for the Voluson E-Series. The IP addresses for the default
gateway and other routers at the site for ROUTING INFORMATION. Only if necessary (e.g. for Internet
access).
1. Press the Utilities key on the control console.
2. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
3. On the right side of the screen select Connectivity and then click the Device Setup tab.
4. Click the button, read the message and confirm with Yes.
1 You can get IP and DNS settings assigned automatically, if your network supports this capability.
2 If fixed IP address is required, ask your network administrator for the appropriate settings.
Type in:
- IP address
- Subnet mask
- Default gateway
- DNS server
Note For further details refer to the Voluson E-Series Basic User Manual.
Note To configure the Voluson E-Series system to work with WLAN, the hospital’s network administrator has to
provide the required information.
Content in this section
3.13.2.1 Connecting to the WLAN - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-59
3.13.2.2 Disconnecting from the WLAN - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-59
3.13.2.3 Adding a WLAN Profile - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-60
3.13.2.4 Refreshing a WLAN Network - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-60
3.13.2.5 Setting a WLAN Network as Non-Preferable - - - - - - - - - - - - - - - - - - - - - - - - - 3-60
3.13.2.6 Removing a WLAN Profile - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-61
3.13.2.7 Customizing an existing WLAN Profile - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-61
3.13.2.8 Available WLAN Channels - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-62
3.13.2.9 Monitoring the WLAN - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-62
3.13.2.10 WLAN Diagnostic - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-63
3.13.2.11 Repairing the WLAN - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-63
Note If the WLAN fails to connect, review and/or recreate the Wireless connection in the Security tab.
- Data Encryption
- Network Key
- Key Index
7. After you have filled in all the required information, click OK.
5 WPA(2) PSK = WiFi Protected Access using one Pre-Shared Key Note: PSK is also referred to as "Personal" encryption standard.
- Data Encryption
- Network Key
- Key Index
7. After you have filled in all the required information, click OK.
6 WPA(2) PSK = WiFi Protected Access using one Pre-Shared Key Note: PSK is also referred to as "Personal" encryption standard.
Note DO NOT cancel the Repair operation after you have selected to repair the Wireless LAN connection.
By means of the Cellular Modem, it is possible to connect the Voluson E-Series to the Internet by using a
SIM card.
Note MMS are sent by e-mail to a 3rd party provider (e.g. SMSglobal). This service needs to be ordered by a 3rd
party provider.
Note Please check with a Smartphone located near the Voluson E-Series, if network coverage is available. Used
SIM card in the Smartphone should use same provider as SIM card for Cellular Modem.
Hardware Setup: To use the feature the peripheral Cellular Modem needs to be installed and a SIM card from
your local service provider needs to be ordered.
Note Since the Voluson E-Series does not enable browser access, the service provider needs to enable the
Internet access on the SIM card before installation in the Cellular Modem. Please ensure from the service
provider, that there is no browser registration necessary when using the SIM card.
Dial in Phone Number e.g., *99# - if not explicitly stated by the provider, use *99#
Please ensure that the SIM card information is available before setting up the Voluson E-Series.
Modem Configuration
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
2. Insert the SIM card into the Cellular Modem.
3. Connect the Cellular Modem as described in Section 3.5.7 on page 3-26 .
4. Press the Utilities key on the control console.
5. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
6. On the right side of the screen select Connectivity and then click the Device Setup tab.
7. Click the Modem Configuration button; see Figure 3-44 on page 3-58 .
The Modem Configuration screen appear.
Note Please keep the Dial information as *99#. Only in seldom cases different Dial information is needed.
9. Check box "Connect automatically".
10. Click OK.
11. Click the signal strength icon in the status bar.
Select Connect for connection to the service provider.
12. Please wait while busy symbol is on screen.
If the connection is established: Tooltip of the status icon provides signal strength in percentage.
If the connection is not established: Tooltip of the status icon provides an error message.
13. Depending on the region and/or provider it might be possible that you need one time registration of
your SIM card, therefore:
a. Open Windows Start Menu - All Programs - Internet Explorer.
b. Internet connection OK: close all open windows.
c. Internet connection fail: enter registration key or voucher code, then close all open windows.
14. If it is desired to send E-mails, perform configuration as described in Section 3.13.4 on page 3-66 .
15. If it is desired to use also MMS, adjust settings as described in Section 3.13.5 on page 3-67 .
16. Assign the Modem to a remote key (P1, P2, P3, P4, P5 and/or P6) as described in Section 3.6.6
"Remote Control Selection" on page 3-41 and adjust the Email settings.
17. Individually enter Patient's Email address and Phone number in the PID screen and adjust Email
and/or MMS options as described in Section 3.13.6 on page 3-68 .
If Internet access is available via LAN, Wi-Fi or Cellular modem, it is possible to send images/cines via E-
Mail to patients or physicians.
Note The Voluson E-Series is only supporting E-mail send; no e-mail receive is possible. To receive reply E-mails,
the same E-mail account needs to be installed on an Office-PC.
Note Maybe the information above needs to be searched in the Internet from your e-mail provider and is the same
for all e-mail users.
Email Configuration
1. Press the Utilities key on the control console.
2. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
3. On the right side of the screen select Connectivity and then click the Device Setup tab.
4. Click the Email Configuration button; see Figure 3-44 on page 3-58 .
The Email Configuration screen appear.
5. Enter Your name and Email Address in the Identity group. As an option you can enter a different Reply
to Address and a Signature Text.
6. To verify E-mail configuration click on Send Test Email. An E-mail is sent to the entered E-mail address
followed by a message box where either a success message or an error message is shown.
7. Store your configuration with click on OK.
8. If it is desired to use also MMS, adjust settings as described in Section 3.13.5 on page 3-67 .
9. Individually enter Patient's Email address and Phone number in the PID screen and adjust Email
and/or MMS options as described in Section 3.13.6 on page 3-68 .
If the Voluson E-Series is connected to the Internet (via LAN, Wi-Fi or Cellular modem) and E-mail service is
configured properly, it is possible to send images as an MMS.
Note MMS are sent by e-mail to a 3rd party provider (e.g. SMSglobal). This service needs to be ordered by a 3rd
party provider.
MMS Options
1. Press the Utilities key on the control console.
2. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
3. On the right side of the screen select Connectivity and then click the Device Setup tab.
4. Click the Email Configuration button; see Figure 3-44 on page 3-58 .
5. In the Email Configuration screen check box "Use Email to MMS Service" and then click on Settings.
3.13.6 How to enter Patient's Email address and Phone number in the PID screen
1. Enter the “Patient ID” screen by pressing the Patient ID key on the control console.
2. Click the @ icon (1).
The Patient´s Email address and Phone number window appear.
Note Since the E-mail to MMS service provider is maybe not located in the same area as your MMS receptions,
you need to add the area code (e.g. +49 or 0049 for Germany) to the used phone numbers in the Patient's
E-mail address and Phone number dialog.
Example: local phone number 069913800000 is +49 69913800000 or 0049 69913800000 for Germany
4. Click the Map Network Drive button to open a dialog where the system can be connected to a shared
network drive of another server.
5. Enter the name of the shared network folder in the „Network Folder Name” field.
6. Supply a valid user name and a password for this folder.
Note If you check the „Automatic Reconnect“ box, the system tries to establish the connection again when starting
up. Otherwise, the connection must be re-established manually after a shutdown or reboot.
7. Select the Connect button to establish the connection to the remote system. If successful, the
Disconnect button becomes active.
Note The Map Network Drive button is also accessible in the “Connect USB and Network Drives” dialog window
that appears when pressing the Eject key on the alphanumeric keyboard.
Note If there is an error during the connection, a warning message appears inside the dialog. In this case, please
verify the data in the dialog.
Note If there already is a connection to the remote server, the Connect button is grayed. To change the existing
connection, first click on Disconnect and then enter the new settings.
Warning
Please make sure that the server you are connecting to is trustworthy and reliable. For details, contact your
local system administrator.
If you backup archive data to this server, all the patients demographic data will be copied to this server!
Configuration Steps
At EC330 (BT18) systems the trackball functions are displayed in the trackball status area of the screen.
Note There are different possibilities to access the Common Service Desktop and its available features; see
Section 5.12.2 "Service Platform - Access and Security" on page 5-48 .
2. Select the Configuration page, then double-click InSite ExC Agent Configuration (A).
3. Fill out at least all bold stated mandatory fields in the Agent Configuration section (B).
- The Device Name (pre-populated) and the CRM field have to be prefix KE6 or KE8 + systems
serial number without prefix letter; e.g. KE810026.
- Select Continent and Country from the pull-down menu.
- Enter City, State, Postal Code and Institution where the system resides.
4. Check settings in the Advanced Configuration section (C).
- Enterprise Server - PRODUCT
- Service Center - EURO
- Log Level - WARN
Further fields should be pre-populated and should not be modified. However, please ensure correct
setting.
- Enterprise Server URL - pre-populated URL
- Enterprise Tunnel URL - pre-populated URL
- File Repository - This path is set by engineering and must not be changed!
- File Watcher - Should always be Enabled!
- Dir - D:\export
- Filter - ensure that this field has the entry "*.zip"
5. Enter Proxy Configuration (D).
a. If the customer site does not require a Proxy server, select Disable from the Proxy pull-down
menu and continue with step 7.
b. If a Proxy server is available, select Enable from the Proxy pull-down menu, enter a valid Proxy
IP Address and Port number.
Note The information MUST be properly entered, otherwise remote control does not work. There is no possibility
to detect proxy server information automatically.
6. Click the Submit Changes button (E) and then close the page.
7. Reboot the system.
8. Reenter the Common Service Desktop (CSD).
9. Confirm that Service Connectivity is "Configured" and "Checked Out" in the Home page.
If the system indicates "Checked Out" you can be confident that the system has registered correctly. If
required, verify further connectivity (e.g., remote connectivity using your account) .
10. Close the page and check/create InSite permanent user setting; see Section 3.13.8.1 on page 3-71 .
5. Fill in the required information and confirm with Add User (4).
6. Check mark the appropriate user and then click Set Default Machine Contact (5).
Color of the selected user turns from BLACK to RED (6). The permanent user is created.
7. Close the window.
3.15 Paperwork
Note During and after installation, the documentation (i.e. User Manual, Installation Manual,...) for the peripherals
must be kept as part of the original system documentation. This will ensure that all relevant safety and user
information is available during the operation and service of the complete system.
Note The provided Product Locater Installation Card may not be the same as shown in the Figure below.
Check that the correct User Manual(s) for the system and software revision, is included with the installation.
Specific language versions of the User Manual may also be available. Check with your GE Sales
Representative for availability.
Functional Checks
This chapter provides procedures for quickly checking major functions of Voluson
E-Series system diagnostics by using the built-in service software, and power
supply adjustments.
Note Most of the information pertaining to this Functional Checks chapter is found in the Voluson E-
Series Basic User Manual; see: Section 9.11 "System Manuals" on page 9-44 .
Note After turning off a system, wait at least 10 seconds before turning it on again. The system may not be able to
boot if power is recycled too quickly.
1. Connect the main power cable to the back of the system.
2. If not already done, screw on the pull-out protection of the mains power cable with the 2 screws.
3. Connect the main power cable to a hospital grade power outlet with the proper rated voltage. Never
use an adapter that would defeat the safety ground.
4. Switch ON the circuit breaker at the rear of the system.
1 circuit breaker
2 fuses (2x T10A H/250V)
3 connector for main power cable
Note When AC power is applied to the system, the ON/OFF standby button on the control console illuminates
amber, indicating that the system (including the Back-end Processor) is in standby mode.
5. Hold down the ON/OFF standby button (see: Figure 4-2 below) on the control console for ~3 seconds.
Note The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the ON/OFF
standby button. The power switch of any attached printer(s) needs to be in ON position before starting the
system. However, be aware some auxiliary equipment may switch itself to standby mode (e.g., Color video
printer) and must therefore be switched on separately.
As soon as the software has been loaded, the system enters 2D-Mode with the probe and application that
were used before the system shutdown. Total time used for start-up is about 2 minutes.
Note The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the ON/OFF
standby button. So the auxiliary equipment need not to be switched ON/OFF separately.
Note After turning off a system, wait at least 10 seconds before turning it on again. The system may not be able to
boot if power is recycled too quickly.
1. If not already in read mode, freeze the image.
2. Press the ON/OFF Standby button on the control console. Following dialog appears.
Note A full shutdown is also performed when pressing the ON/OFF standby button on the control console twice.
Note The mains outlet of the system for peripheral auxiliary equipment are commonly switched with the ON/OFF
standby button. So the auxiliary equipment need not to be switched ON/OFF separately.
Warning
Disconnection of the main power cable is necessary!
5. After complete power down, unscrew the 2 screws and remove the pull-out protection to disconnect the
main power cable from the system or unplug it from the AC wall outlet socket.
1 circuit breaker
2 fuses (2x T10A H/250V)
3 connector for main power cable
Caution
Do not disconnect a probe while running (Live Scan “Write” mode)! A software error may occur. In this case
switch the system OFF (perform a reset).
3 Mode keys on/off (push), Gain (rotate) 10 button for control console rotation
X,Y,Z rotary controls in 3D/4D Volume Mode
4 Foc.Depth (flip), B-Image Angle (rotate), Foc.Zones (push) 11 buttons for control console height adjustment
5 Zoom Box on/off (push), Zoom Size (rotate), B-Image Depth 12 Voluson Logo
(flip)
6 Remote control P-keys (programmable) 13 alphanumeric keyboard and F1 key (to invoke EUM)
2 Shows all presets for the active application; the active one is highlighted.
4 Settings which can be adjusted by the combination rotary/push/flip controls adjacent to the Touch Panel.
The functionality of these controls changes, depending upon the currently displayed menu.
Note Different menus are displayed depending on which Touch Panel Menu and which Mode is selected.
It might be possible that some probes, options or features are NOT available
• in some countries.
• at the time of release of this Service Manual.
Note Some software may be considered standard depending upon system configuration. If any Modes or Options
are not part of the system configuration, the check can be omitted.
Note Different menus are displayed depending on which Touch Panel Menu and which Mode is selected.
Note Some function keys only appear on the Touch Panel if they are available for the selected probe.
The Voluson E-Series provides an Patient/Image Management System that allows fast and extremely easy
patient, exam and image management.
Current Patient:
The entered patient data will be used in calculations, patient worksheets, DICOM settings and is displayed
on the screen to identify images.
Archive:
The patient archive database is used for searching a particular exam and/or patient. Via the Data Transfer
button, it is possible to send images over the DICOM network, print exams/images, export exams/images,
import exams/images, etc.
Image History:
Image History gives you access to all the US pictures and exams of a particular patient.
Exam Review:
Exam Review allows you to view all exams of a particular patient. Additionally it is possible to view image
properties, input comments and voice annotations, etc.
Note For further details refer to the Voluson E-Series Basic User Manual.
Note Images can also be backed up and restored by means of the Image Archive function in the System Setup.
Operation see Section 4.4.6 on page 4-20 .
6. Choose the media (2) and click the Save button (3).
7. Select the New File... key and enter a file name (without extension).
8. Click the OK key to start the process. When the saving has been completed, click OK.
The loading procedure overwrites existing image/scan settings on the local hard drive.
Make sure to insert the correct System DVD. Additionally you can load the image settings from “D:
\UserSettings”.
4.4.2.1 Preparations
1. Insert a DVD/CD+R/RW into the drive or connect an external USB device.
2. Press the Utilities key on the control console.
3. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
4. On the right side of the screen select Backup and then click the System Configuration tab.
5. Click the Load button (1) of the "Small Backup (Scan Settings)" group.
6. Choose the media (2) and click the Load button (3).
Note If it is desired to load settings from media Internal HDD, click on the Change folder button, browse for the
folder on “D:\usersettings” and then click the Load button.
7. Select the appropriate file and click OK.
8. Select the desired loading procedure:
- "Load "Complete Backup"" on page 4-13
- "Load only parts of the "Complete Backup"" on page 4-14
3. Click the Load button (3) to start the loading procedure of the complete backup into the system.
The US Application Software restarts.
3. For example: Click the [+] sign and copy the desired content by clicking the [>>] button; and so on ....
Note To return selected items from the “Load Data” field to “Backup Data” field select the [<<] button.
4. Confirm selection with the Load button (3).
Settings will be loaded and the US Application Software restarts.
A backup of the Full System Configuration always contains the following data
• User Settings (databases and files containing User Programs, 2D/3D/4D Presets, gray curves etc.)
• System Settings (general "Setup" settings such as Language, Time/Date format, Button configuration,
Annotation settings, Biopsy lines, Peripheral data, Video Norm, Archive configuration, etc.)
• Measure Configuration (user specific measure setup settings)
• User Authentication Data (User Authentication Configuration (user names, group names), LDAP
configuration, audit trail configuration,...)
• Patient Archive (database containing patient demographic exam data and measurements) - no images
• V830 Settings (Options resp. Permanent Key that is specific for enabled software options and Demo
Key)
• Image Transfer Configuration (DICOM configuration e.g., DICOM servers, AE Title, Station Name, etc.)
• Network Configuration (Network settings: IP address, Network Profiles, e-mail configuration, network
printer, network drives, computer name)
• Service Platform (state of the Service Software)
Note It is recommended to “Full Backup” system configuration data before upgrading the software and/or image
settings (presets). This ensures that if settings need to be reloaded, will be the same ones the customer was
using prior to service.
1. Press the Utilities key on the control console.
2. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
3. On the right side of the screen select Backup and then click the System Configuration tab.
4. Click the Save button of the "Full System Configuration" group.
5. Choose the destination (1).
Note Image data will not be backed up! To backup the Image Archive, refer to Section 4.4.6 on page 4-20 .
7. Click the Next button (3).
8. To start the backup process click Yes.
After copying the data, the Voluson E-Series reboots and the application starts again.
When the “Full Backup” is saved on a network drive it may be desirable to move the data (e.g., for backup or
maintenance). To map a network drive see Section 3.13.7 on page 3-69 .
The backups reside in sub folders of the main “fullbackup” -folder found at the root of the drive.
For Example: Backups on the mapped Network Drive are below path Z:\fullbackup.
The directory structure of the full backup data is as follows:
The sub folders have the names fbX where X is a number (e.g.,
Z:\fullbackup\fb1).
The data resides within a directory structure within these sub
folders. It is possible to move the fbX sub folders, even leaving
gaps in the numeration sequence.
However, NO change MUST be made to the contents of the fbX
folders itself, otherwise the backup data cannot be restored!
If the destination „Other drive“ is selected, the available drives (e.g., external
USB-memory stick) can be chosen from the pull-down menu.
Note When the backup is saved to an external USB-device, the system has to be informed about the removal of
the hardware. For this purpose every last dialog of "Full Backup Save" and "Full Backup Delete" has a Stop
USB Devices button.
For further details see Section 3.5.15 "General Remarks when using external USB-Devices" on page 3-35 .
Caution
It is recommended to backup data before an upgrade; see Section 4.4.3 on page 4-15 .
The “Full Backup” loading procedure replaces (overwrites) ALL existing data (except Application Settings
adapted for the used system software version) on the local hard drive of the Voluson E-Series system!
Note It is neither required nor advisable to reload a previously stored “Full Backup” after a software upgrade that
was performed by means of the FMI from DVD button!
Note There are circumstances where it is not possible to load (restore) all the data. The following rules specify
these restrictions:
1. Generally, only restoring data from an older to a newer software version is possible. Loading a backup
into a system that has a lower software version than the system the backup was created on is
prohibited.
2. Options can only be restored on the same Voluson E-Series system within the same major software
version.
3. When loading a backup into a system with a software version that has a higher major number (e.g.,
15.x.x -> 16.x.x -> 17.x.x), the following items will not be restored:
- Options
- State of the Service Platform
4. The user is only allowed to restore data to a different system if and only if the software version on this
system is the same as in the backup.
5. The user is not allowed to restore the following items to a different system:
- Windows Network Settings
- Options
- DICOM AE Title and DICOM Station Name
- State of the Service Platform
Operation
1. Press the Utilities key on the control console.
2. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
3. On the right side of the screen select Backup and then click the System Configuration tab.
4. Click the Load button of the "Full System Configuration" group.
5. Choose the destination (1).
6. Click on the backup to be restored (2). Additional information is displayed in the table.
7. Select the Next button (3).
The following window will be displayed.
Note For description of the check box names see Section 4.4.3 on page 4-15 .
Note When User Authentication Data is checked, a dialog asking for the system administration password appears.
Enter the correct password and click OK. Select Cancel to close the dialog. (The User Authentication Data
check box becomes unchecked.)
9. Click the Next button and then select Yes to start, or No to cancel the restore procedure.
Caution
When clicking Yes, the current data on the system will be permanently replaced by the data of the backup
and can not be restored!
After restoring the data, the Voluson E-Series reboots and the application starts again.
6. Click on the backup to be deleted (2). Additional information is displayed in the table.
7. Select the Delete button (3).
Caution
There is no "Undo" function for this action!!!
Note It is highly recommended to Backup the Full System Configuration (Section 4.4.3 on page 4-15 ) and the
Image Archive (Section 4.4.6 on page 4-20 ) once a week.
Note If for example “All images older than” 1 Day is chosen (see: Figure 4-21 on page 4-20 ), images of the
current day will not be archived! However, if you click the [Advanced] button you can put this right.
6. If desired, check mark “Remove Local Images after Backup” (3).
7. Click the Advanced button (1) if it is desired to adapt archive data.
Note Voluson E-Series presets, configurations and image settings will not be backed up! To Backup the Full
System Configuration see Section 4.4.3 on page 4-15 .
11. Select the Next button (7).
12. To start the backup process click Yes.
8. Select (check mark) the image archive data to be restored to the Voluson E-Series system (4).
9. Select the Next button (5) and then select Yes to start, or No to cancel the restore procedure.
4.5.1 Setup
Note Almost all settings have to be assigned as desired and required by the customer. After completion, return the
equipment to the customer and ensure acceptance.
Note For further details refer to the Voluson E-Series Basic User Manual.
General Settings
1 General: Check Date and Time setting Date and Time are correct
2 General: Check that Clinic Name is correct Clinic Name (location) is correct
Administration
1 Options: Check that all options are set up correct D = Demo , I = Inactive , P = Permanent
Connectivity
1 Peripherals: Check the Video Norm standard as setting assigned as required for the country
described in Section 3.7.1.6 on page 3-45 .
2 Device Setup: Check DICOM, Archive and Network settings assigned as desired and required by the
configuration nodes (e.g., TCP/IP, WLAN, EMAIL, etc.) customer
Backup
not applicable
Imaging Pesets
Assign all (further) settings as desired and required by the customer.
Biopsy
not applicable
Measure
Assign all (further) settings as desired and required by the customer.
2 Press the remote key (P1, P2, P3, P4, P5 or P6), The image displayed on the screen is printed on the
which is assigned to the BW printer. Black & White printer.
3 Press the remote key (P1, P2, P3, P4, P5 or P6), The image displayed on the screen is printed on the
which is assigned to the color printer. Color printer.
4 Press the remote key (P1, P2, P3, P4, P5 or P6), Recording starts/stops.
which is assigned to recorder control.
1 Press the Utilities key on the control console and then It will display a curve along the bottom edge of the
touch the ECG button to display the “ECG” menu. image sector.
The control console can be rotated, translated and adjusted in height (electronically only).
Note For further details refer to Section 5.10.3 on page 5-46 and/or Section 6.3 on page 6-4 .
The Voluson E-Series used digital beamforming technology which provides high resolution and high
penetration performance. It is a general purpose, mobile, software controlled diagnostic ultrasound system.
Its function is to acquire ultrasound data and to display the data of different modes gives the operator the
ability to measure anatomical structures and offers analysis packages that provide information that is used to
make a diagnosis by competent health care professionals.
The Calculation and Report function supports following application packages:
• Abdominal (ABD)
• Obstetrical and Fetal Echo (OB)
• Gynecological (GYN)
• Small Parts and Breast (SM P)
• Vascular (VAS)
• Pediatrics (PED)
• Transrectal (TR)
• Cardiology (CARD)
• Cephalic (CEPH)
• Musculoskeletal (MSK)
The Voluson E-Series supports a variety of linear-, curved-, phased array and pencil CW probes for various
clinical applications.
Any 3 probes may be connected at the same time (+ 1 pencil CW probe).
Medical application fields include:
• Obstetrics
• Gynecology and Fertility
• Radiology
• Internal Medicine
• Neurology
• Cardiology
• Oncology
• Urology
• Orthopedics
• Pediatrics
The system is designed for follow-up expansion.
In addition to the initial operational settings for each probe preprogrammed in the system, user-customized
parameter settings for each probe may be inserted by the operator and stored for recall as needed via the
system control console. System configuration is stored on the hard drive and all necessary software is
loaded from the hard drive on power up.
Biopsy guidelines are provided on screen to assist in the collection of tissue samples, using biopsy guide
adapters offered as an optional accessory.
The system provides the ability to perform remote viewing of images without compression, via DICOM 3.0
compatible output. Management of patient history is possible by image-filing function. High-resolution images
are provided by utilizing a technology called digital dynamic receive focusing.
For more detailed explanations of functions and controls refer to the Voluson E-Series Basic User Manual.
5.1.1.1.2 XTD-View
XTD-View (Extended View) provides the ability to construct and view a static 2D image which is wider than
the field of view of a given probe. This feature allows viewing and measurement of anatomy that is larger
than what would fit in a single image. XTD-View constructs the extended image from individual image frames
as the operator slides the probe along the surface of the skin in direction of the scan plane. Examples
include scanning of vascular structures and connective tissues in the arms and legs.
5.1.1.1.3 B-Flow
B-Flow is especially intuitive when viewing blood flow, for acute thrombosis, parenchymal flow and jets. It
helps to visualize complex hemodynamics and highlights moving blood in tissue. B-Flow is less angle
dependent, no velocity aliasing artifacts, displays a full field of view and provides better resolution when
compared with Color-Doppler Mode. It is therefore a more realistic (intuitive) representation of flow
information, allowing to view both high and low velocity flow at the same time.
5.1.1.2 M-Mode
In M-mode, soft tissue structure is presented as scrolling display, with depth on the Y-axis and time on the X-
axis. It is used primarily for cardiac measurements such as value timing on septal wall thickness when
accurate timing information is required. M-mode is also known as T-M mode or time-motion mode.
Ultrasound echoes of different intensities are mapped to different gray scale values in the display. M-mode
displays time motion information of the ultrasound data derived from a stationary beam. Depth is arranged
along the vertical axis with time along the horizontal axis. M-mode is normally used in conjunction with a 2D
image for spatial reference. The 2D image has a graphical line (M-line) superimposed on the 2D image
indicating where the M-mode beam is located.
5.1.1.5 3D Imaging
The Voluson E-Series Ultrasound System will be used to acquire multiple, sequential 2D images which can
be combined to reconstruct a three dimensional image. These 3D images are useful in visualizing three-
dimensional structures, and in understanding the spatial or temporal relationships between the images in the
2D sequence. The 3D image is presented using standard visualization techniques, such as surface or
volume rendering.
5.1.1.8 3D Rendering
The 3D (volume) rendering is a calculation process to visualize certain 3D-structures of a scanned volume by
means of a 2D-image. The gray value for each pixel of the 2D-image is calculated from the voxels along the
corresponding projection path (analyzing beam) through the volume. The render (calculation) algorithm,
surface or transparent mode, determines how 3D-structures are visualized.
This section describes the functions of the boards vs. different operation modes.
• RFM - (RF-Interface & Beamformer) FE Mainboard
• RSX - (Beamformer Receiver/Transmitter) Extension Board
• RTV - Video Management Board
5.1.3.1 B-Mode
1. IF-FPGA
The RFM contains the Clock-Management and PRF-Generator. It generates (drives) Shot-Trigger for
the BF-FPGAs. Configures the BF-FPGAs of RFM and RSX with Tx-Frequ, Tx-Focus, Rx-Focus,
LineNo (lateral Position), Tx- Apodisation, RX-Apodisation, Multibeam, etc.
Furthermore it contains Multibeam-DeInterleave, Subtraction Filter (for HI-Mode, see Section 5.1.3.1.1
"Special B-Mode Techniques" on page 5-10 , DC-Canceler, Mixer (Part of Demodulator),
LowPassFilter and Decimation (Pixel rate Conversion).
After DC-cancelling the signal is mixed with RX-Frequency and brought to LF-Spectrum, where the
LowPassFilter cuts HF. Mixer and Magnitude-Calculator arrange Complex Demodulation, and
Logarithmic Amplifier arrange the conversion from High-Dynamic LinearSignal to the Low-Dynamik(e.g.
8Bit) Log-Signal. Several postprocessing steps (LineFilter, FrameFilter, ReSample, Edge Enhance)
enable smooth image quality while keeping contrast high.
a. Direct Memory Access (DMA) section
B-mode data from RFM is written via Signal Processor (SP) Channel 0 into SDRAM Fifo Buffer
memory. DMA Controller 0 transfers the data into PC main memory where scan conversion is
performed per software. Cine Mode: Reserved area in PC main memory is used.
2. BF-FPGAs
Each BF-FPGA handles Rx/Tx of 64 channels. It controls 16 Tx-pulsers and 8 AFE ICs (i.e.: 32 Tx-
pulsers and 16 AFE ICs each on RFM and RSX board).
The AFE consists of Low Noise Amplifier (LNA), Rx-TGC-Amplifier, Signal-ADC. Each pulser can
support 4 Tx-channels, each AFE can support 8 Rx-channels.
- Tx-channel: The BF-FPGA generates Tx-Freq through dividing 200MHz by 2,3,4,5,... and Tx-
Focus.
- Rx-channel: The clock distribution generates Sample-Clocks for the ADC (50 MHz). The BF-
FPGA manages Rx-Focus (Delay and Chain-Adder) and Apodization.
3. RTV - Video section
Video Information is provided by the PC on the DVI (Digital Visual Interface) output connector. The
signal is connected to RTV, where the analog VGA signals for the monitor and standard video timing
outputs are generated.
5.1.3.2 M-Mode
1. IF-FPGA
see: Section 5.1.3.1 "B-Mode" on page 5-10
2. RTV - Video section
see: Section 5.1.3.1 "B-Mode" on page 5-10
It might be possible that some probes, options or features are NOT available
• in some countries.
• at the time of release of this Service Manual.
BT15 BT16
(EC300) (EC310)
VE10
VE10
VE6
VE8
VE6
VE8
HCat # Software Option Description
H48681GD Advanced STIC (incl. Basic STIC, STIC M-Mode Advanced STIC (Spatio-Temporal Image - 2) 2) - 2) 2)
and STIC flow) + SonoVCAD heart Correlation)
H48691YA eM6C - E4D Activation (incl. eSTIC) eM6C - E4D Activation (Advanced Features for - - X - - X
Electronic 4D Matrix-Probe)
Legend:
- not available
S Standard Feature, S* can be used in 3D-Mode, but for 4D-Modes the option “Advanced 4D” has to be active as well
1) this 3D/4D option can be used in 3D-Mode, but for 4D-Modes the option “Advanced 4D” has to be active as well
BT17 BT18
(EC320) (EC330)
VE10
VE10
VE6
VE8
VE6
VE8
HCat # Software Option Description
H48691XZ HDlive Silhouette and Studio HDlive Silhouette and HDlive Studio - 1) S* - - -
H48681GD Advanced STIC (incl. Basic STIC, STIC M-Mode Advanced STIC (Spatio-Temporal Image - 2) 2) - 2) 2)
and STIC flow) + SonoVCAD heart Correlation)
H48691YA eM6C - E4D Activation (incl. eSTIC) eM6C - E4D Activation (Advanced Features for - - X - - X
Electronic 4D Matrix-Probe)
H48701WM Advanced Security Features (incl. Disk Encryption Advanced Security Features - - - X X X
and Whitelisting)
Legend:
- not available
S Standard Feature, S* can be used in 3D-Mode, but for 4D-Modes the option “Advanced 4D” has to be active as well
1) this 3D/4D option can be used in 3D-Mode, but for 4D-Modes the option “Advanced 4D” has to be active as well
5.1.4.1 Advanced 4D
5.1.4.2 HDlive
Most current surface reconstructions use an illumination frontal to the rendered object. This can cause the
image to look flat. HDlive Rendering uses an illumination source that can be positioned by the user around
the rendered 3D object on a spherical surface. By highlighting structures from the side, the three-
dimensional impression is improved considerably.
Note "HDlive" is part of the “Advanced 4D” option for Voluson E8 systems. At Voluson E6 systems it is optional
(separately purchasable). At Voluson E10 systems it is not available.
5.1.4.8 Elastography
Elastography refers to the measurement of elastic properties of tissues, based on the well-established
principle that malignant tissue is harder than benign tissue.
Elastography shows the spatial distribution of tissue elasticity properties in a region of interest by estimating
the strain before and after tissue distortion caused by external or internal forces. The strain estimation is
filtered and scaled to provide a smooth presentation when displayed.
During scanning in the elastography mode, the examiner manually slightly compresses the tissue using the
ultrasound probe. A strain correlation (strain is the deformation of the tissue by compression) is continuously
performed for visual perception on the monitor.
Note “SonoVCAD heart” is part of the “Advanced STIC” option for Voluson E8 and Voluson E10 systems. At
Voluson E6 systems it is optional (separately purchasable).
Note “STIC” is part of the “Advanced STIC” option for Voluson E8 and Voluson E10 systems. At Voluson E6
systems it is optional (separately purchasable).
Note The “V-SRI” option is only available at Voluson E10 systems with probe RM6C, RIC5-9-D and RIC6-12-D.
5.1.4.16 SonoMetrium
SonoMetrium allows automated detection and display of a rendered Uterine C-plane and thereby 3D
analysis of the endometrial cavity in application Gyn.
This option is only available for Voluson E-Series systems with software version EC330 (BT18).
5.1.4.17.1 eSTIC
The intended use and workflow of the eSTIC acquisition mode is the same as the standard STIC mode but
with the advantage of a faster acquisition time.
This option is only available for Voluson E-Series systems with software version EC330 (BT18).
Note Any data stored on internal HDDs D:\ partition is encrypted by using BitLocker configured with AES 256-bits
key length.
Caution
Without the Encryption Password or Recovery Key it will not be possible to access the Ultrasound device
including emergency mode, scanning, patient information, images, or local archive. GE has no access to this
information or the ability to undo encryption in the event that the Encryption Password and Recovery Key are
lost. The security and safety of the Encryption Password and Recovery Key is solely the user's responsibility.
Note The "Disk Encryption” option is only available for Voluson E-Series systems with software version EC320
(BT17, requires Ext.4 or higher). At Voluson E-Series systems with software version EC330 (BT18), Disk
Encryption is part of the Advanced Security Features option.
Note A Voluson E-Series systems without the option but with encrypted disk is unlockable.
5.1.4.22.1 Whitelisting
Whitelisting prevents the Voluson E-Series system from installing unwanted software. It monitors all
applications/services if they are known and accepted (white-listed). Any application/service that is not known
on the system creates an error message on the screen.
"Whitelisting” is only available for Voluson E-Series systems with software version EC330 (BT18). It is part of
the Advanced Security Features option.
If more than one IOTA option (i.e., IOTA LR2, IOTA Simple Rules) is available, it is possible to configure the
measure setup which worksheet is displayed.
IOTA LR2
The IOTA (International Ovarian Tumor Analysis) LR2 Worksheet contains an ovary measurement tool for
women with adnexal tumors that have been selected to undergo surgery. The LR2 model is based on
published literature and has been tested only on the stated population. The literature states that the LR2
model can help to estimate the probability of an adnexal mass of being malignant. The IOTA group has
evaluated other ways including an LR1 model in additional to the LR2 model.
Note IOTA states that use outside of the intended population can overestimate risk. Users are expected to study
the literature and reach their own professional conclusions regarding the clinical utility of the tool. The model
cannot replace experience in ultrasonography and cannot compensate for poor quality ultrasound
equipment.
The IOTA mathematical logistic regression model, LR2 is stated in literature as described in the Advanced
Reference Manual (H48701UU).
General Electric is passing on this IOTA LR2 worksheet for your convenience based on published literature
of one group, but makes no representation of its effectiveness in your practice. This calculation is not to be
used as the primary driver in diagnostic decision making on the probability of malignancy. It is secondary
information for a physician to use based on recent literature.
The "IOTA Simple Rules" option is only available for Voluson E-Series systems with software version EC330
(BT18).
HW-Options Description
3 WLAN Network Adapter Wireless Network Adapter (WLAN - Wireless Local Area Network)
The Voluson E-Series Hard disk drive (HDD) is divided into 4 partitions:
C: System partition:
• Operating System (Windows 7 at EC300-EC320, Windows 10 at EC330) including all Windows
settings (IP-address, Network Name, etc.)
• US-Application Software (UISAPP)
• Global Service Platform Software
• Software Options
D: User partition:
• User Presets (Backup) database
• Images (Archive), Patient-ID´s and Reports database
• Service database
• System settings database
R: Rescue partition:
• Factory Images of C: Partition for System recovery after HDD (Windows) crash
• Printer Drivers
LINUX partition: (not visible in Windows)
• Linux operating system for rescue functionality
This board is not applicable at BT17 (EC320, 17.x.x) and BT18 (EC330, 18.x.x) systems.
• EC300/EC310 (BT15/BT16):
The FrontEnd Mainboard supports Tx/Rx for 128 channels only. To extend to 192 or 256 channels, the
RSX - (Beamformer Receiver/Transmitter) Extension board is required.
• EC320/EC330 (BT17/BT18):
The FrontEnd Mainboard supports Tx/Rx for 192/256 channels. It does not need RSX Extension board.
This board is not applicable at BT17 (EC320, 17.x.x) and BT18 (EC330, 18.x.x) systems.
Note All components of RSX board are also present on RFM - (RF-Interface & Beamformer) FE Mainboard.
5.3.1 PC-Motherboard
The Hard Disk is the main storage device of the Voluson E-Series ultrasound system.
The Voluson E-Series hard disk drive is divided into 4 partitions.
For further details see Section 5.1.6 "Data Location" on page 5-22
Graphic Card which supplies RTV (Video manager) board with digital video. It offers dynamic contrast
enhancement and color stretch video processing optimized on a scene by scene basis for spectacular
picture clarity.
Distributes Video signal information coming from the Graphic Card to the DVI respectively HDMI connectors.
Converts DVI/HDMI inputs to S-Video output(s).
• DVI to HDMI input (RTV30) respectively HDMI to HDMI input (RTV35) connection to Graphic Card
• DVI output (RTV30) respectively VGA output (RTV35) for external device (only RGB signals used)
• HDMI output for external device
• S-Video output for external devices
• USB connector for board configuration
Note The “Mainboard type” can be read out in the Setup - Administration - SYSTEM INFO page (see Figure 7-1
on page 7-3 ).
Figure 5-7 Internal I/O Voluson E-Series BT15 (EC300): PC-Motherboard Micro-ATX ADVANTECH + RTT/RTH6x
Figure 5-8 Internal I/O Voluson E-Series BT15/BT16 (EC300/EC310): PC-Motherboard Micro-ATX ADVANTECH + RTH50
Voluson E-Series Service Manual
5539550APB Revision 6 5-29
Components and Functions (Theory)
Figure 5-9 Internal I/O Voluson E-Series BT15 (EC300): PC-Motherboard Flex-ATX KONTRON + RTT/RTH6x
Figure 5-10 Internal I/O Voluson E-Series BT15/BT16 (EC300/EC310): PC-Motherboard Flex-ATX KONTRON + RTH50
Voluson E-Series Service Manual
5539550APB Revision 6 5-31
Components and Functions (Theory)
Figure 5-11 Internal I/O Voluson E-Series BT17 (EC320): PC-Motherboard ADVANTECH Micro-ATX
Voluson E-Series Service Manual
5-32 5539550APB Revision 6
Components and Functions (Theory)
Figure 5-12 Internal I/O Voluson E-Series BT18 (EC330): PC-Motherboard ADVANTECH Micro-ATX
Figure 5-13 Internal I/O Voluson E-Series BT18 (EC330): PC-Motherboard KONTRON Micro-ATX
The Voluson E-Series control console (User Interface) consists of the following electronic sub-assemblies
and/or functional components:
• Display/Touch screen module:
- WXGA display - 1280 x 800 pixels
- Integrated USB to Video converter with USB2.0 High Speed Interface
- projected capacitive touch screen
• Console module:
- 7 port USB 2.0 Hub controller
- Contols (Encoder/Joycoder) with integrated rotary/push/flip function
- USB Trackball (2”) with dedicated buttons to emulate standard three button mouse
- USB standard alphanumeric keyboard
- USB extended keyboard with controller
- LED Indicators with wide range dimming
- LED to illuminate probe port connectors
• DC/DC Converter:
- Converts 12VDC input voltage to 5VDC and 3.3VDC output voltage for supplying User Interface
components
7 Archive (Review) opens the Patient archive and/or exam review mode
8 End Exam stores patient and measurement data and clears all temporary data
21 ABC (Text) activates the annotation function in order to add comments to an image
23 Bodymark activates the annotation function in order to add body patterns to an image
29 P2 programmable key
30 P4 programmable key
31 Auto Automatic Optimization (optimizes the image based upon the actual BMode
image data)
33 P1 programmable key
34 P3 programmable key
59 Trackball button left left trackball key (function depends on currently selected mode)
60 Trackball button top top trackball key (function depends on currently selected mode)
61 Trackball button right right trackball key (function depends on currently selected mode)
62 Trackball button bottom bottom trackball key (function depends on currently selected mode)
63 UI Brake (Movement) Locks and releases the horizontal movement of the user interface
116 Lift DOWN Height adjustment (lift down) of the user interface
5.6 Monitor
For further details see Section 6.2.2 "Loading the Default Monitor Settings" on page 6-3
Figure 5-18 RTH6x => "white" USB2.0 ports / RTH50 => "blue" USB3.0 ports
Figure 5-19 External I/O connectors - on the left/right side of the Monitor
1
USB USB 3.0 port
2
Note For further description of I/O connectors refer to Section 3.9 "External I/O Connectors" on page 3-50 .
5.8 Peripherals
Note There are no recording tools available and released for the Voluson E-Series system.
5.8.2 Printers
Caution
Laser radiation: Avoid exposure to the beam Class 3B laser product.
Class 3B laser radiation: When open avoid exposure to the beam.
DVD Drive
The DVD Drive (Writer) is used to backup images and reports. In addition, it is used as the main source of
software upgrades and other service utility operations. It is controlled by the BEP via USB port.
Software DVR
The SW-DVR (SoftWare Digital Video Recording) function is optional at EC300-EC320 (BT15-BT17)
systems and enables video recording to DVD media or USB devices.
Media supported for data burning Media supported for video recording
• DVD+R • DVD+R
• DVD-R • DVD-R
• DVD-RW • DVD-RW
• DVD+RW • DVD+RW
• CD-R • all Dual Layer formats
• CD-RW • USB stick or external USB HDD drive (FAT32 or NTFS system)
Note A minimum writing speed of 2 MByte/sec is required to ensure stable video recording on USB devices.
Lower writing speed can result in audio and/or video drop outs. The use of USB3.0 devices is recommended.
The ECG-preamplifier is used for acquiring an ECG-signal to be displayed with the ultrasound image. This
optional peripheral serves for gaining an ECG-signal to mark the systolic and end diastolic moments in M-
Mode and Doppler evaluations.
The ECG-preamplifier must not be used for ECG-diagnostics. It is not intended for use as a cardiac monitor
and must not be used for an intra-operative application on the heart.
The Voluson E-Series supports a Wireless Network USB Adapter based on industry standards to provide
easy-to-use and compatible high-speed wireless connectivity. For details regarding type and installation, see
Section 3.5.8 "Connecting the Wireless Network Adapter" on page 3-28 .
The Wireless Network USB Adapter provides a mobile network connection to the local area network.
5.8.6 Footswitch
The Footswitch is used for comfortable system control when no hand is free. To adjust function of the
Footswitch (Left/Middle/Right) see Section 3.7.1.8 on page 3-45 .
Connecting the Voluson E-Series to the Internet allows the user to send images via e-mail and/or MMS to
patients or physicians. Whenever no LAN or Wi-Fi Internet connection is available, it is possible to connect
the Voluson E-Series to the Internet by using the optional Cellular Modem. To use this feature the peripheral
Cellular Modem needs to be installed and a SIM card from your local service provider needs to be ordered.
For details regarding installation and configuration see Section 3.13.3 on page 3-64 .
The Voluson E-Series system has a free adjustable LCD Flat panel monitor in relation to the user interface.
Press the Brake button inside of the handlebar opening to rotate/translate the console to the
desired position. Press the Brake button again in order to secure the console against
uncontrolled movement.
Height adjustment is done with the Lift UP / Lift DOWN button inside of the handlebar opening.
As long as a button is pressed, the control console can be lifted / lowered.
Caution
Make sure that nothing would be jammed while moving!
Through the filter grid on the back of the system (Main Air Inlet), air flow into the Voluson E-Series system.
• Air holes in the RSP power supply allow the air to pass through; the 3 fans inside the RSP suck in the
air and spread it through the beamformer.
• By means of the 2 Backend fans, air is blown through the GEB-box (along its internal components and
the PC- Motherboard).
The warm air exits the system through holes in the left side panel (Main Air Outlet).
5.12.1 Introduction
InSite is the connectivity to the Voluson E-Series system that allows GE to deliver remote diagnostics
capability. InSite is your direct link with a GE Online Service Engineer or Applications Support Engineer, or a
Request for Service via the InSite link (GE icon) at the right bottom of the display screen.
The GE icon in the status bar change symbol and color depending on ongoing activity; see Table 7-3 on
page 7-13 .
The Service Platform has different access and security user levels. Each user is only granted access to the
tools that are authorized for their use.
There are different possibilities to access the Common Service Desktop and its available features:
• Local Access : via Setup - Administration - Service page
• Remote Access: This offers GE technicians the possibility to view the entire customer's desktop and
operation system. Remote access to the Voluson E-Series system requires permission and customer
input to run diagnostics.
The Common Service Desktop (CSD) is started and the Home page - containing basic System Information -
appears. The navigation bar at the top of the screen allows to select different tools.
For more detailed information see Section 7.6 "Common Service Desktop (CSD)" on page 7-14 .
Internationalization
The user interface provided by the service platform is designed for GE personnel and as such is in English
only. There is no multi-lingual capability built into the Service Interface.
There are different possibilities to access the Common Service Desktop and its available features:
• Local Access : via Setup - Administration - Service page
• Remote Access: This offers GE technicians the possibility to view the entire customer's desktop and
operation system. Remote access to the Voluson E-Series system requires permission and customer
input to run diagnostics.
As soon as the Common Service Desktop (CSD) is started, the Service Home Page appears.
The navigation bar at the top of the screen allows to select from different tools for troubleshooting/
adjustment. For detailed description see Section 7.6 "Common Service Desktop (CSD)" on page 7-14 .
5.14.1 Introduction
The Service Page contains specific software/hardware test modules, system setup,update, etc. for Voluson
E-Series systems only.
The service page has different access and security user levels. Each user is only granted access to the tools
that are authorized for their use.
Please observe that the displayed screens may slightly differ from images shown in this manual. The
availability of some functions or features depend on the BT-version of your Voluson E-Series system.
Note For intermittent problems this file can be requested from the Service Engineer or customer. It is possible to
burn this file on DVD/CD+R/RW.
Operation see Section 7.7 "How to use the Auto Tester program" on page 7-18 .
Note During “FMI from DVD” the used system configuration (incl. Full Backup) will be stored on R:\. If required, the
previously used System configuration (before FMI from DVD was performed) can be restored by activating
the “Rollback” function. Operation see: Section 5.15.3 on page 5-53 .
Note Please make sure that ONLY the DVD writer is connected on the USB ports. Disconnect all other external
USB devices (such as printers, hubs, bluetooth, memory devices) as this might interfere with the recovery/
installation procedure.
Note Existing User Programs, 3D/4D Programs and Auto Text remain unaffected! Therefore it is not necessary to
perform any readout preparations.
Warning
If you select the YES button, all patients data, studies, images and measure report data will be deleted
permanently from the hard disk and cannot be recovered!
Note When reloading these Application Settings, any existing User Programs, 3D/4D Programs and Auto Text
remain unaffected!
1. Click Load Application Settings on the “Service Tools” page (see Figure 5-27 on page 5-50 ).
2. Choose the media and then click Load.
Note If the ID of the Application Setting is not valid for the currently installed Application Software version, a
warning message appears during boot up sequence.
4. If warning message is displayed, confirm it with OK and then load appropriate Application Settings
(perform loading procedure as described in steps above).
Voluson
GE-Service
Rollback
Memtest (Memory Check)
After 3 sec. without pressing any key, the system will boot-up in windows (= Voluson item). If you missed
selection, retry again with Ctrl + Alt + Del.
5.15.1 Voluson
The System will boot-up in windows. The Ultrasound Application is started. For details see Section 3.4.1.1
"During a normal boot, you may observe" on page 3-11 .
5.15.2 GE-Service
5.15.3 Rollback
This function offers the possibility to simply restore the previously used system configuration (rollback), which
was stored on R:\ during “FMI from DVD”.
1. Turn system OFF and then back ON.
2. As soon as the “Boot Screen” appears (see: Figure 5-30 on page 5-53 ), press the [PgDn] (Arrow
down) key on the keyboard until the Rollback item is highlighted, then press Enter.
3. When the following WARNING message appears, press the [<-] (Arrow left) button to highlight OK and
then press Enter.
After performing the rollback, the system reboots. The Ultrasound Application is started and finally the 2D
screen is displayed on the monitor.
After 3 sec. without pressing any key, the system will boot-up in windows (= Voluson item). If you missed
selection, retry again with Ctrl + Alt + Del.
The PC Memory Test starts automatically and takes about 2.5 hours. If there are errors they will be listed.
Note After one cycle (~ 2.5 hours) the memory check starts again. To interrupt the test, press the Esc key. If you
don't interrupt the memory test , it will perform never ending cycles of memory checks.
Note If after one cycle (about 2.5 hours), no error messages are listed, it can be assumed that the Back End
Processor including power supply is working properly.
Service Adjustments
This chapter describes how to test and adjust the mechanical capabilities of a
system that may be out of specification. Although some tests may be optional
they should only be performed by qualified personnel.
6.1 Regulatory
Verify, where applicable, that any regulatory information or tests required by national law are present and
accounted for, and any regulatory tests required by national law are performed and documented.
Incline the monitor Move back and forth Move up and down
Move the upper monitor arm parallel to the lower arm and push it down (1), then lock it by turning the knob (2) counterclockwise.
Release by turning the knob clockwise.
Rotate the arm to center position and turn the knob (1) clockwise till the rotation is locked. Release by turning the knob
counterclockwise.
To ensure that no part of the monitor can be damaged when transporting or moving the system, the monitor
has to be in a secure position.
1. Lock all monitor parts.
2. Incline the monitor to horizontal position.
The system can now be safely transported. Nevertheless be careful when transporting or moving the device.
3. Touch the Semi-Dark Room button to load default monitor settings for your system.
Press the Brake button inside of the handlebar opening to rotate/translate the console to the
desired position. Press the Brake button again in order to secure the console against
uncontrolled movement.
1 Lift UP / Lift DOWN button for height adjustment of the control console
Caution
The system should not be moved with the control console (UI) extended. Do not put your hand between the
control console and the main unit when moving the control console to its centered and locked position:
Danger of injuries!
Height adjustment is done with the Lift UP / Lift DOWN button inside of the handlebar opening.
As long as a button is pressed, the control console can be lifted / lowered.
Caution
Make sure that nothing would be jammed while moving!
Note Shipping the Voluson E-Series ultrasound system in its original packaging is only possible when control
console is centered and locked in position, the system is lowered to its minimum height and the monitor is
flapped down and locked (see Figure 6-1 on page 6-3 ).
Modification of the Keyboard Layout is no more possible at systems with operating system Windows 10
(software version EC330, BT18).
Note Configuring the layout of the keyboard is only useful by changing the concerned keys also; see Section 8.13
"Replacement of Key Caps (by special native language keys)" on page 8-24 .
Keyboard Layout Modification procedure depends on the operating system (Windows 7 or Windows 10).
Note If the desired language is not listed, click the Add button, choose the desired input language from the pull-
down menu, as shown in Figure 6-6 below, and then confirm with OK.
Diagnostics/Troubleshooting
This chapter describes how to setup and run the tools and software that help
maintain image quality and system operation. Basic host, system, and board level
diagnostics are run whenever power is applied. Some Service Tools may be run
at the application level.
Note All the above information can be found in the "System Info" page; see: Figure 7-1 on page 7-3 .
Note Move the scroll bars downwards to view additional information about the installed software/hardware.
Press the Ctrl + H key simultaneous to display the shortcuts list and a description of what they do.
Alt + D export system state (Full Backup and Alt + F7 start/stop process logger
Dump files) to D:\export
Ctrl+ Alt + D Factory use ONLY! This function is Ctrl + F8 Factory use ONLY! This function is
not intended for the user. not intended for the user.
Ctrl + H shortcuts list (see: Figure 7-2 above) Shift + F9 start remote socket control
Ctrl + Alt + I start/stop presentation mode Alt + F9 stop remote socket control
Alt + P stores screenshot on D:\export Shift + Ctrl + F11 Factory use ONLY! This function is
not intended for the user.
Ctrl + S User Program save Crtl + Alt + F11 Factory use ONLY! This function is
not intended for the user.
Ctrl + V paste, insert text from clipboard Shift + Insert insert text (paste)
Shift + Ctrl + F1 save Logfile snapshot Shift + Print Fast Export all
Screen
Move the cursor to the InSite link (GE icon) at the right bottom of the display
screen and press the left trackball key (= left-click). The “Contact GE” form (see
Figure 7-3 below) is displayed.
Note If the service platform is not configured an Error message is displayed. The request is NOT sent!
The LED within the start key (ON/OFF button) on the User Interface is used to signal the status of the
Voluson E-Series system.
The following states are implemented:
FPGA_CONF_DONE = low
blinking
IF-FPGA not initialized -> probably FrontEnd (RFM board) or Power Supply
Orange <=> Green
(RSP) issue
On the backside of the ATX board near the fans 3 green status LEDs are mounted. These LEDs are used for
signaling the status of the Power Supply (RSP).
Boot up diagnostic LEDs behind the right side door should help to diagnose system issues easier.
1 5V Standby
2 Configuration done
3 PC Power OK
4 HDD status
ON OFF
5V Standby (green) • 5V Standby voltage available from Power • 5V Standby voltage not available
supply (RSP) • No mains voltage, mains power cable not
• If in parallel the ON/OFF button of the console connected
is dark then the line up to the Console is • System is switched off (circuit breaker off)
interrupted (RSP -> RTB -> RTT -> RTU). • Power supply (RSP) defective
Configuration done • Configuration of the FrontEnd was successful • FrontEnd FPGA was not initialized correctly ->
(green) probably issue with RFM-Board
• In this state the ON/OFF button of the console
is blinking (orange <-> green)
• Further boot up is continued without FrontEnd
hardware.
PC Power OK (green) • PC was started, ATX supply voltages are • PC was not started correctly
switched on (the PC has got ATX-Power) • RSP could not send „Start PC“ Signal, PC did
not send „PS_ON“ signal
• All cables/connectors between Power supply
(RSP) and PC should be checked
• BackEnd (PC-Board) or Power supply (RSP)
could be defective
HDD Status (red) • Access to the hard disk (normally blinking) • No access to the hard disk
useful to observe hard disk activities • Depending on the status of the system software
hang-ups can be confirmed
The following is the generic process to capture any screen from the Voluson E-Series system.
1. Navigate to, and display the image/screen/volume to be captured.
2. Press the P1, P2, P3, P4, P5 or P6 key (depending on system configuration) on the control console
and store the image onto the clipboard (frame on left side of the screen).
Note A short summary of P1, P2, P3, P4, P5 or P6 keys configuration is shown in the status area on the screen.
3. Select the stored image(s) and export them to DVD drive, an external USB drive (optional) or mapped
Network drive (jpg, bmp, tiff or Volume file).
The Full Backup created by Alt + D is protected by a password that can be customized. Whenever
transmitting system state to R&D, do not forget to inform them about any password change.
Data can be stored on the hard disk (D:\export\fullbackup\fb1), or you can export them to DVD/CD, etc.
Including the D:\export folder, which contains dump files (for details see Section 7.4.2.2.1 on page 7-11 ),
Autotester script files, SMART logs, sniffer logs and screen shots (Alt + P).
Note Successive Alt + D keystrokes overwrite existing snapshots at destination (Internal) HDD.
1. Press the Alt + D key on the keyboard simultaneously.
2. Select whether you want to backup data with our without hardware diagnosis tests.
Please detach all probes if you want to execute hardware diagnosis, then click Yes.
7.5.1 General
This allows GE technicians to view the entire customer´s desktop and operation system. Using VCO (Virtual
Console Observation) a service technician or the OLC (OnLine Center) can access and modify all settings
and programs or run diagnostics on the customer's Voluson E-Series system.
When Voluson E-Series systems can be serviced remotely, service costs are minimized, and customers
benefit from decreased costs and decreased downtime for their systems.
Note Remote access is ONLY possible if the Service Platform is properly configured (either by the user or a GE
technician at site). Operation see Section 3.13.8 "InSite Configuration" on page 3-70 .
Remote access to the Voluson E-Series system requires permission and customer input before a GE service
technician or OLC can access the customer's system remotely.
Disruptive Mode can be selected by the customer directly on the Voluson E-Series (see Section 7.5.2 on
page 7-13 ), or requested remotely by the service technician or OLC .
5. Select Cancel respectively Disconnect to turn OFF “Disruptive Mode” and “VCO”.
Note Visual information about GE remote status is shown in the status area on the right bottom of the screen. At
EC330 (BT18) systems the trackball functions are displayed in the trackball status area of the screen.
EC330 only: Move the cursor over the GE icon to show trackball functions
• Contact : Section 7.2 "Request for Service (RFS)" on page 7-5
• Configuration: Section 3.13.8 "InSite Configuration" on page 3-70
• Menu: Displays the Remote Access (Disruptive Mode) menu
Yellow = Access Remote Access connection is active, but Disruptive Mode and Virtual Console
pending Observation (VCO) is not yet enabled.
Red = Disrupted Remote Access is active. All processes [UL_VNC and UL_CSD] are active. In this
State state the Voluson E-Series system should NOT be used clinically.
Note If the customer does not wish to have diagnostics running at the time of the request, select Cancel. A
message is sent back to the OLC or FE that permission to change Disruptive Status is denied.
Whenever any hardware diagnostic tests have to be executed on site, the CSD must be accessed via the -
All Programs - Voluson -GE Field Engineer - Common Service Desktop.
The navigation bar at the top of the screen shows the top level menu choices.
Note As described in Section 5.13 on page 5-49 , the service platform uses a web-based user interface to provide
access to common service components. The Service platform is designed for GE personnel and as such is
in English only. There is no multi-lingual capability.
Content in this section
7.6.1 Error Logs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-14
7.6.2 Diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15
7.6.3 Image Quality - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15
7.6.4 Calibration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15
7.6.5 Configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15
7.6.6 Utilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-16
7.6.7 Replacement - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-17
7.6.8 PM - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-17
When the Error Logs page is selected, different log viewing options are available.
Select the Log Viewer option in the left pane of the Error Logs page. Available logs are displayed in a
separate window.
7.6.2 Diagnostics
7.6.4 Calibration
7.6.5 Configuration
In the Configuration page, you can view and modify different device informations.
Note Remote access is ONLY possible if the Service Platform is properly configured (either by the user or a GE
technician at site). Operation see Section 3.13.8 "InSite Configuration" on page 3-70 .
7.6.6 Utilities
The Utilities page contains a variety of Windows utility tools to indicate the status of the system, in addition to
various other tools.
Disruptive Mode
Allows to enable or disable disruptive mode.
Disk Usage
All drives (real & virtual) mounted on the system will be shown in the right frame. Each drive will display the
total size in bytes and the total number of free bytes.
IP Configuration
Windows IP Configuration: The TCP/IP information for the device + all real and virtual networking interfaces
are displayed.
Network Status
All ports (listening & established) are displayed along with any external/foreign address that might be
connected to the device.
Windows Services
The currently active windows services (applications) are displayed.
User Accounts
Shows the internal account information that was provided and set up on the system by the OLC.
Shared Resources
Indicates the resources being shared by the system.
Disk Defragmenter
Shows how to execute a Disk Defragmentation.
Dicom Verify
This enables to verify DICOM devices.
7.6.7 Replacement
7.6.8 PM
6. Click OK.
7. Press the Alt Gr key on the alphanumeric keyboard.
8. Activate the “Auto Tester” program by clicking the “Record” icon on the displayed screen.
9. Start scanning. You can scan normally and everything will be recorded to the program (up to several
hours).
Note It is important that you are recording the processes where the errors normally occur.
Stop the program by clicking on [Stop] shown on the screen, or by pressing the Alt Gr key
on the alphanumeric keyboard.
10. Select the “Save” icon. The file will be saved in D:\Export\AutotesterScripts\*.*.
11. Press Alt + D to export system data and the needed logs. Operation see Section 7.4.2.1 "Export
System Data (by pressing the ALT + D key)" on page 7-10 .
Note The standalone recorded "Auto Tester" file makes only sense with the Alt + D log! To analyze the workflow
the exact date and time of occurrence needs to be documented!
12. If desired, save the script file also on DVD/CD. Therefore:
- Insert an empty DVD/CD+R/RW in the Drive and select the “Burn on CD” icon.
- Enter a Filename.
- After the DVD/CD write is finished click the OK button.
13. Close the “Auto Tester” program.
The following information will not be recorded. Depending on the moment the Auto Tester is activated, this
must be provided by the customer or the field engineer.
• Which probe is in use and which probes are connected?
• Which Mode is activated?
• Which peripherals are connected (Dicom, Printer, etc..)?
Collected information from all steps above + exported system data and needed logs (Alt + D) can be sent to
the Make Center. With this information the Make Center can see how the customer is using the system and
reproduce potential failures.
Note Providing all information at once will help the Make Center find the root cause and speeds up finding a
solution for the customer.
If a stand-alone UPS (Uninterruptible Power Supply) is available to power the Voluson E-Series
Connect the UPS between AC mains and the Voluson E-Series system in the same manner as shown in
Figure 7-28; - instead of the stand-alone Power Filter.
1. Switch on the Voluson E-Series system.
2. Activate the ultrasound probe and choose settings which show EMC noise in the ultrasound image to
check for EMC noise (EMC noise should be visible).
3. Disconnect one by one all cords that are connected to the Voluson E-Series system like LAN/Ethernet,
VGA, DVI, S-Video, USB, ... on the ultrasound system-side and observe the EMC noise.
4. If EMC noise is still present after disconnecting all cables, then disconnect the AC mains power cord
that supplies the UPS from the wall outlet socket.
If EMC noise is absent, then it is confirmed that the EMC noise source is in the power line of the wall
outlet socket.
5. If EMC noise is still present – then check again for any other conducting connections to the Voluson E-
Series; perform step 3.) again.
6. Connect one by one other cords to the Voluson E-Series system like LAN/Ethernet, VGA, DVI, S-
Video, USB, ... and check for EMC noise.
If EMC noise does not depend on whether the ultrasound probe is contacted
When the EMC noise does not depend on whether the ultrasound probe is contacted (hold in hand/apply to
body), then do the following:
1. Hold the ultrasound probe only at the cable and change the orientation of the ultrasound probe.
2. If the EMC noise changes by changing the orientation of the ultrasound probe then the EMC noise is
caused by a magnetic field in the room/building.
In such situations the Power Filter (H48701EL) cannot reduce the EMC noise.
Connect an USB-Mouse to one of the USB-Connectors of the Voluson E-Series system (the USB connectors
beside the DVD-Drive are recommended). So the system remains operable until the trackball problems are
solved.
Picture is fuzzy Adjust the picture contrast and picture brightness. Some SVGA cards having an
excessive video output level will cause a fuzzy picture at the maximum contrast
level.
Note For further details see Section 6.2 "LCD Monitor Adjustment" on page 6-2 .
a. Click on Export.
b. If not already selected, choose “DVD/CD” resp. "DVD Rec" from the pull-down menu.
c. Enter "File name".
d. Select any Voluson Format (*.4dv) from the pull-down menu.
e. Click the Save button.
Limits: All images, which have been exported to DVD/CD+R/RW are visible.
Press the Eject key on the alphanumeric keyboard and remove the media from the drive.
Note If you use an unformatted DVD+RW, recording is impossible! To format the DVD, press the DVD key and
then select the Format button.
2. Press the PW key on the control panel to start PW preparation mode.
3. Activate Doppler motion display by pressing the right/left trackball key.
4. Press the DVD key on the control console once to display the remote control menu.
5. In the remote menu touch the Record button to record a Doppler motion display (e.g., of the Carotid).
6. Touch the Stop button to stop recording.
7. Touch the Finalize button. The recorded motion sequence is stored on DVD.
8. Touch the Play button to play-back the recorded Doppler motion sequence.
With the Skip buttons the next/previous sequence can be selected.
Limits: The recorded Doppler motion sequence is running. The audio signal of the arterial flow can be heard in the
loudspeaker(s).
Green = Cable connected to a network. Does not imply proper network settings.
1. Check that the network cable between the Voluson E-Series system and the wall network is connected
and well seated in both ends. (Use a network cable that is known to be OK.)
2. Connect a network cable between the system and a PC by either using a hub or a cross-over cable.
Try to ping from system to IP address on PC. If OK, hardware connection inside the system is OK.
EC330 only: Move the cursor over the GE icon to show trackball functions
• Contact : Section 7.2 "Request for Service (RFS)" on page 7-5
• Configuration: Section 3.13.8 "InSite Configuration" on page 3-70
• Menu: Displays the Remote Access (Disruptive Mode) menu
Yellow = Access Remote Access connection is active, but Disruptive Mode and Virtual Console
pending Observation (VCO) is not yet enabled.
Red = Disrupted Remote Access is active. All processes [UL_VNC and UL_CSD] are active. In this
State state the Voluson E-Series system should NOT be used clinically.
Issue: In case of network connectivity issues, it may not be possible to activate your Windows operating system on the
Voluson E-Series systems. Monitor screen display: Activate Windows. Go to Settings to activate Windows.
Note: When present, the "Activate Windows" message will not impact system performance in any way.
Solution: 1. Check Operating System License Status in Utilities - Setup - Administration - System Info tab.
a. Licensed -> Windows is properly activated.
b. Notification -> Windows is not activated. Proceed with troubleshooting steps.
Issue: Storing SonoView images from Voluson 730/Expert/Pro/ProV to Voluson E-Series systems.
Solution: 1. Perform SonoView backup on Voluson 730/Expert/Pro/ProV to external hard disk (USB) or DVD.
2. Import file "V730.mdb" from external hard disk (USB) or DVD to your Voluson E-Series system.
Procedure
1. Connect the external hard disk (USB) or insert the DVD with the SonoView backup to the Voluson E-
Series system.
2. Enter “Patient Archive” by pressing the Patient ID key on the control console.
Replacement Procedures
This chapter contains replacement procedures for different modules and their
subsystems.
Note The Manpower, time and Tools indicated in the Sub-sections include all requirements from
Preparations to Installation Procedures.
Warning: DO NOT touch any boards with integrated circuits prior to taking necessary ESD
precautions.
1. When installing boards, ESD may cause damage to a board. ALWAYS connect yourself, via
an arm-wrist strap, to the advised ESD connection point located on the rear of the system (to
the right of the power connector).
2. Follow general guidelines for handling of electrostatic sensitive equipment.
Warning
No covers or panels should be removed from the system (high-voltage risk). Service and repairs
must only be performed by authorized personal. Attempting do-it-yourself repairs invalidate
warranty and are an infringement to regulations and are inadmissible acc. to IEC 60601-1.
The Waste of Electrical and Electronic Equipment (WEEE) must not be disposed as
unsorted municipal waste and must be collected separately. Please contact the
manufacturer or other authorized disposal company for information concerning the
decommission of your equipment.
Note For control console positioning see Section 6.3 on page 6-4 .
Equipment being returned must be clean and free of blood and other infectious substances.
GE policy states that body fluids must be properly removed from any part or equipment prior to shipment. GE
employees, as well as customers, are responsible for ensuring that parts/equipment have been properly
decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids
be taken or shipped from a clinic or site (for example, body coils or and ultrasound probe).
The purpose of the regulation is to protect employees in the transportation industry, as well as the people
who will receive or open this package.
Note The US Department of Transportation (DOT) has ruled that “items what were saturated and/or dripping with
human blood that are now caked with dried blood; or which were used or intended for use in patient care”
are “regulated medical waste” for transportation purpose and must be transported as a hazardous material.
Note The user/service staff should dispose of all the waste properly, per federal, state, and local waste disposal
regulations.
The Voluson E-Series system is not meant to be used for long-term storage of patient data or images. The
user is responsible for the data on the system and a regular backup is highly recommended.
If the system is sent for repair, please ensure that any patient information is backed up and erased from the
system before shipping. It is always possible during system failure and repair to lose patient data. GE is not
responsible for the loss of this data.
If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes, GE will
ascertain agreement from the customer. Patient information shall only be transferred by approved service
processes, tools and devices restricting access, protecting or encrypting data where required, and providing
traceability in the form of paper or electronic documents at each stage of the procedure while maintaining
compliance with cross-border restrictions of patient information transfers.
Caution
Disconnecting ALL external USB devices (except DVD drive) is NECESSARY. Re-installation of any
previously attached printer has to be done after the upgrade procedure.
Note Installing the Bluetooth Printer and its connection set is NOT possible by the user.
Manpower
One person ~ 1 hour (depends on contents of System DVD resp. SW update package, peripherals, etc.)
Tools
System DVD
Note It is NOT necessary to save Full System Configuration (Full Backup) prior to the upgrade. All existing User
Programs, 3D/4D Programs and Auto Text settings remain untouched!
Figure 8-1 Version check: System Setup - Administration - System Info page
5. Select the Option tab to see which options are currently installed. Please print out the options page or
write down down the state of the options (P = permanent, I = inactive).
Note It is not necessary to note the Permanent Key; it is the state of the option that matters.
1 D = Demo (Option is activated for demo and expires at date shown in the "Valid" column)
I = Inactive (Option is not activated)
P = Permanent (Option is permanently activated, i.e.purchased)
d = deactivated (Option is inactive)
2 Permanent Key
Note If the currently installed software has to be upgraded to a newer version, and the system is updated via the
FMI from DVD button, a new software specific “Permanent key" is required. Please contact your local
distributor or GE service representative.
The system software installation procedure starts with saving and recording the settings present on the
system (silent “Rollback”). Then the new software is written to the hard disk using the System DVD.
Application Settings are automatically updated, to match with new Software version.
Existing User Programs, 3D/4D Programs and Auto Text remain unaffected! Afterwards the new software is
configured such that it is integrated again in its environment.
Note For more detailed information, see Section 5.14.3.3 "FMI from DVD" on page 5-51 .
1. Perform Preparations as described in Section 8.2.1 on page 8-4 .
2. If not already done, disconnect all external USB devices (except DVD drive).
3. Insert the System DVD into the drive.
4. Restart the system. (Turn system OFF and then back ON.)
Note If the system boots into LINUX, the “Boot priority order” in BIOS is incorrect. In this case, cancel the software
installation procedure (select Exit/Reboot by means of the [Arrow] keys (right, left, up, down) and the [Enter]
key on the keyboard) and then contact your service representative.
5. Press the Utilities key on the control console.
6. In the “Utilities” menu touch the Setup button to invoke the setup desktop on the screen.
7. On the right side of the screen select Administration and then click the Service tab.
8. Enter the password « she » and click Accept.
9. Click the FMI from DVD button for updating the System Software.
10. Verify that only the DVD drive is connected to the system, then click OK.
Figure 8-4 Verify that USB devices are disconnected, then click OK
Note If the currently installed software has to be upgraded to a newer version, a new software specific “Permanent
key is required.
12. Enter the appropriate “Permanent Key” (calculated in OKOS; http://3.187.187.9/OKOS), select OK and
confirm with Enter.
If the entered Permanent key is correct, following window appears, confirm with Enter.
New Format from EC310 onwards: Previous Format still valid until EC300:
17. Please wait until all processes are finished (100 percent completed).
18. The system is rebooting into windows (Boot screen - Voluson).
Note An automated process was developed to install the required software parts, perform check disk, remap drive
letters and match settings. During this process the system might reboot several times!
19. Please wait until all processes are finished. Finally the 2D screen is displayed on the monitor.
20. Remove the System DVD from the DVD/CD+R/RW Drive drive.
21. If the Touch panel is not working after first boot up, please shutdown the system; then boot up again.
Note After turning off a system, wait at least 10 seconds before turning it on again. The system may not be able to
boot if power is recycled too quickly.
22. Reconnect the external devices, install all the printers and adjust the printer settings as described in
Section 3.6 "Printer Installation" on page 3-36 .
23. Check and match Printer Remote Control selection in the Setup - Connectivity - Button Configuration
page.
24. Confirm date and time setting in the Setup - General Settings - General page.
25. Perform Software and Functional checks as described in Section 8.3 on page 8-14 .
Overview
This icon (at right bottom of the screen) indicates that a new Software Update
Package is available for download and installation.
An InSite permanent user is required for automatic system error reporting to the digital service network; see
Section 3.13.8.1 "How to create an InSite permanent User" on page 3-71 .
The system software installation procedure starts with saving and recording the settings present on the
system (silent “Full Backup" and "Rollback”). Then the new software is written to the hard disk. Application
Settings are automatically updated, to match with new Software version.
Existing User Programs, 3D/4D Programs and Auto Text remain unaffected! Afterwards the new software is
configured such that it is integrated again in its environment.
Update Procedure
1. Remove any CD/DVD from the DVD drive.
2. Perform Preparations as described in Section 8.2.1 on page 8-4 .
3. If not already done, disconnect all external USB devices (except DVD drive).
4. Press the ON/OFF Standby button on the control console.
5. In the displayed screen click Download.
6. Download takes some time; please wait. (Download my be paused by means of the Pause button.)
7. When download is finished, click Install.
Note Installation may take up to one hour. DO NOT interrupt the installation!
If you want to install the new software later, click Exit. Installation can be resumed by clicking Install (in the
Shutdown window).
A silent “Rollback” image from C:\ is stored on R:\. After executing all LINUX commands, the system
reboots again.
10. 3 dots (one after the other) appear on the screen.
11. Booting auto ....
13. Please wait until all processes are finished (100 percent completed).
14. The system is rebooting into windows (Boot screen - Voluson).
Note An automated process was developed to install the required software parts, perform check disk, remap drive
letters and match settings. During this process the system might reboot several times!
Finally the 2D screen with the "New Software Verification" report is displayed on the monitor.
16. Reconnect the external devices, install all the printers and adjust the printer settings as described in
Section 3.6 "Printer Installation" on page 3-36 .
17. Check and match Printer Remote Control selection in the Setup - Connectivity - Button Configuration
page.
18. Confirm date and time setting in the Setup - General Settings - General page.
19. Perform a check of all modes and features listed. (Move the cursor over the feature name to get
information how to check.)
20. When all features are OK enter your signature and then click Send; see: Figure 8-18 above.
Note If one feature gets "Failed", rollback the installation (restore the previously used system configuration). For
more detailed information, see Section 5.15.3 on page 5-53 .
Note It is neither required nor advisable to reload a previously stored “Full Backup” after a software upgrade that
was performed by means of the FMI from DVD button! If the Tune version does not match the Application
Software version, a warning message appears whenever booting up the system. In this case, it is essential
to load the proper Application Settings (image presets), adapted for the installed software version. Refer to:
Section 5.14.3.14 "Load Application Settings" on page 5-52 .
8. Perform basic functional checks to ensure system is functioning normally.
9. Check Service Connectivity; if required, perform InSite Checkout. i.e., Service platform has to be
configured properly; see Section 7.6.5 "Configuration" on page 7-15 .
Loading Procedure
see: Section 4.4.2 "Load Small Backup (Scan Settings)" on page 4-12
Loading Procedure
see: Section 4.4.4 "Load Full System Configuration (Full Backup)" on page 4-17
Loading Procedure
see: Section 4.4.6.2 "Load Image Archive" on page 4-22
It might be possible that some probes, options or features are NOT available
• in some countries.
• at the time of release of this Service Manual.
1 D = Demo (Option is activated for demo and expires at date shown in the "Valid" column)
I = Inactive (Option is not activated)
P = Permanent (Option is permanently activated, i.e.purchased)
d = deactivated (Option is inactive)
2 Permanent Key
4. Position the cursor inside the input field desired and press the right/left trackball key.
5. If one exists, clear/edit the current Permanent Key.
6. Enter the encrypted Permanent Key with the keyboard and click on Submit. (Code will be checked.)
7. Click the Save&Exit button.
Note After activating a Permanent Key, restart (turn off and on) the Voluson E-Series system.
New Format from EC310 onwards: Previous Format still valid until EC300:
Manpower
One person, 1 minute
Tools
none
Preparations
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
Figure 8-21 turn quick release devices 90° and remove the footrest cover
Manpower
One person, 5 minutes
Tools
none
Preparations
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
Manpower
One person, 1 minute
Tools
none
Preparations
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
Manpower
One person, 1 minute
Tools
Phillips screwdriver PH1 and PH2
Preparations
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
Manpower
One person, 3 minutes
Tools
Phillips screwdriver PH1 and PH2
Preparations
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
2. Remove the Printer Flap as described in Section 8.8.3.3.1 on page 8-20 .
3. Remove the Voluson covering and rectangular covering strip (Front Frame) as described in Section
8.8.2.1 on page 8-18 .
Tools
Phillips screwdriver PH1 and PH2
1. Loosen 2 screws below the control console and then remove the Cable Holder.
2. Place the new Cable Holder at its original position and fasten it with 2 screws.
Tools
none
1. Simply pinch the clip and then pull out the Probe Holder to be replaced.
Tools
Phillips screwdriver PH1 and PH2
1. Loosen 3 screws and then remove the Probe Holder for Endocavity probes.
2. Place the new Probe Holder at its original position and fasten it with 3 screws.
Tools
none
Manpower
One person, 30 minutes
Tools
small-sized slotted screwdriver or tweezers
Preparations
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
1. Place a small slotted screwdriver between the Key Cap to be removed and its neighboring Key Cap.
2. Gently lift the Key Cap, until it is completely loosened from its base.
1. Carefully place the appropriate Key Cap in position on the keyboard, taking care to place the plastic
alignment pin in the correct position so that the Key Cap is the right way up and reads correctly.
2. Push the Key Cap down until it snaps into position.
3. Power On/Boot Up the system as described in Section 4.2.1 on page 4-3 .
4. Setup the Keyboard Language Layout as described in Section 6.4 on page 6-5 and then type with the
keyboard to check the function of each key.
Tools
none (poss. small-sized slotted screwdriver or tweezers)
Manpower
One person, approx. 1 minute/cap
Tools
small-sized slotted screwdriver or tweezers
3. Place the new Key Cap down until it snaps into position.
Tools
small-sized slotted screwdriver
Preparations
1. Power Off/Shutdown the system as described in Section 4.2.2 on page 4-4 .
1. Open the fuse protection at the power inlet block (1) with a small-sized slotted screwdriver.
Manpower
One person, 30 - 60 minutes (depending on peripherals)
Tools
slotted screwdriver
Preparations
Content in this section
8.17.1 Mounting/Replacing a Secondary "Patient" Monitor - - - - - - - - - - - - - - - - - - - - - - 8-29
Caution
A Secondary "Patient" Monitor MUST NEVER be connected to the Voluson E-Series systems mains supply
directly! Always connect it to an appropriate Isolation Transformer (see Section 9.10.3 on page 9-42 ).
Warning
After each installation, the leakage currents have to be measured according to IEC 60601-1, IEC 62353 or
other relevant standard.
Note A Secondary Monitor is NOT intended for diagnostic use. It is an additional device used to allow the patient
to watch the proceedings.
Caution
For changing the input/output voltage or fuses the isolation transformer should not be connected. The wrong
fuses and position of the input/output voltage selector may cause major damage on connected peripherals.
1. Before using the Isolation Transformer you must check the input/output voltage settings to meet the
ratings of the line power available in your location or country.
2. For changing the input/output voltage, remove the label by means of a small socket wrench.
3. Switch both voltage selectors (input as well as output voltage) to 115V or 230V. Consider that changing
the input/output voltage also requires to change the fuses!
4. For changing the fuses, open the fuse protection at the power inlet block with a small screwdriver,
remove the fuse holder and exchange fuses.
5. Assure that the connected loads can be operated with the chosen voltage.
Caution
A Secondary "Patient" Monitor MUST NEVER be connected to the Voluson E-Series systems mains supply
directly! Always connect it to an appropriate Isolation Transformer (see Section 9.10.3 on page 9-42 ).
Caution
The transformer must be out of the reach of the patient. However, it needs to be within cable length from the
monitor and a socket. The transformer is IPX 0. There is no protection against ingress of liquids!
Caution
All necessary modifications to wall and buildings must be performed by a professional to avoid structural
damage and electrical hazard.
Note If you need to change the configuration of the newly installed monitor, please, refer to the manual of the
Secondary Monitor, which is enclosed in the Wall mount kit.
Note The monitor needs to be switched of separately at the main power switch of the monitor.
Renewal Parts
This chapter gives an overview of replacement parts available for the Voluson E-
Series system.
It might be possible that some probes, options or features are NOT available
• in some countries.
• at the time of release of this Service Manual.
Assy Assembly
DC Direct Current
FE FrontEnd
Int Internal
I/O Input/Output
UI User Interface
100 - "Housing - Mechanical Hardware Parts & Covers" on page 9-4 Housing Covers (except UI and Monitor), Caster
Wheels, Handle
200 - "User Interface" on page 9-9 Console (keyboard, trackball, display, special knobs
and switches) Loudspeakers, Disk Drive, Probe
holder, Console Covers, etc.
300 - "Monitor + Monitor Replacement Parts" on page 9-17 Monitor + Monitor Replacement Parts
600 - "Options and Upgrades" on page 9-28 Software Options and Upgrades
900 - Probes
- "2D-Probes - Curved Array Probes" on page 9-49
- "2D-Probes - Linear Array Probes" on page 9-51
- "2D-Probes - Phased Array Probes" on page 9-52
- "Real-Time 4D Volume Probes" on page 9-53
- "CW-Doppler - Pencil Probes" on page 9-56
102 Side Cover incl. Door (left) KTZ303548 Side Cover left (incl. Door for probe cables) EC300 1 N Y
103 Side Cover incl. Door (right) KTZ303554 Side Cover right (incl. Door for probe cables) EC300 1 N Y
105 Front Cover KTZ303559 Front Cover EC300 incl. Plug Support 1 N Y
107 Front Frame KTZ303557 Front Frame (Voluson covering + rectangular covering 1 Y Y
strip) EC300
108 Printer Flap incl. Hinges KTZ303815 Printer Flap (incl. Hinges) EC300 1 N Y
109 Printer Box Extension (for KTZ303932 Additional Printer Box for Color Printer A6, EC300 1 N Y
Color Printer)
113 Handle Base KTZ303568 Handle Base EC300, replaced by KTZ304045 (Handle 1 N Y
complete)
114 Handle Bar KTZ303570 Handle Bar EC300, replaced by KTZ304045 (Handle 1 N Y
complete)
115 Handle complete EC300 KTZ304045 Handle complete (Handle Bar + Handle Base) EC300, 1 N Y
replaces KTZ303568 + KTZ303570
119 Caster front ("Steinco") KTZ303911 Caster front (lockable, 2 pcs.) EC300 2 N Y
122 Caster front universal KTZ304057 Caster front, 2 pcs. (lockable) incl. hexagon bolts, 2 N Y
("Tente") washers, lock-nuts and quick fastener
123 Caster back universal KTZ304058 Caster back, 2 pcs. (1 pcs. is lockable) incl. hexagon 1/1 N Y
("Tente") bolts, washers and lock-nuts
Note DO NOT mix "Steinco" and new universal "Tente" Casters. Please identify the used Casters before ordering!
201 Cable Holder KTZ134656 Probe Cable Holder (1 pcs.) for Voluson E-Series 2 N Y
202 Probe Holder Set KTZ303933 Probe holder Set RTU100 (Probe holder inlet left/right, 1 Y Y
Gel holder inlet and holder for Endocavity probe left)
203 Probe Holder right KTZ304030 Probe Holder for Endocavity probe right) 1 N Y
207 Caps Alphanumeric Keyboard KTZ303965 Caps Alphanumeric Keyboard RTU100, English 1 Y Y
210 Caps for Encoder and KTZ303937 Caps for Encoder and Joycoder RTU100 5/7 Y Y
Joycoder
214 Top Cover RTU100 KTZ303938 Top Cover RTU100; incl. 3 Voluson logo stickers 1 N Y
220 Disk Drive3 DVD+(R)W - KTZ303258 DVD+(R)W Writer internal (no own cabinet) 1 N Y
SATA
224 USB3.0 Cable RTU100 KTZ304048 Cable USB3.0 (from RTH50 to external USB connectors 2 N Y
beside DVD Drive at Top Console) 2 pcs.
231 Labels UI, VE6, VE8, VE10 KTZ304103 Labels for User Interface (Voluson logo stickers, 3 pcs. 1 Y Y
each for VE6, VE8 and VE10)
233 Console Touch with Housing KTZ303948 Console Touch with Housing RTU100; without any 1 N Y
electronics
236 Front Key Board with cable KTZ303966 Front Key Board with cable RTU100 1 N Y
301 Monitor OLED 22" (MDM300) KTZ304059 22" Color Image OLED Monitor complete 1 N Y
complete
302 Monitor Back Cover Set KTZ304102 Monitor Back Cover Set MDM3xx (22" OLED Monitor 1 Y Y
MDM3xx
8 only)
303 Monitor Arm (Ergotron) - 22" KTZ304101 Monitor Arm (Ergotron) for 22” OLED Monitor 1 N Y
OLED
8 Monitor Back Cover depends on the currently installed "OLED" Monitor Arm type (MDT30 or Ergotron). If the Monitor Arm is replaced by the other Monitor Arm type, the
Monitor Back Cover needs to be exchanged too (i.e., ordered separately, KTZ304102).
304 Monitor Arm (Daeil) MDT30 - KTZ304069 MDT30 Monitor Arm (Daeil) for 22” OLED Monitor 1 N Y
22" OLED
305 Monitor Color LCD 23” KTZ303839 23” Color Image LCD Monitor complete 1 N Y
(MDM200) complete
307 Monitor Housing Set KTZ303951 Monitor Housing Set for 23" LCD Monitor 1 N Y
308 Monitor Back Cover Set KTZ304090 Monitor Back Cover Set MDM2xx (23" LCD Monitor only) 1 Y Y
9
MDM2xx
9 Monitor Back Cover depends on the currently installed Monitor Arm type (MDT20 or Ergotron). If the Monitor Arm is replaced by the other Monitor Arm type, the Monitor
Back Cover needs to be exchanged too (i.e., ordered separately, KTZ304090).
309 Monitor Arm (Daeil) MDT20 - KTZ303879 MDT20 Monitor Arm (DAEIL) with trapezoidal mounting 1 N Y
23" LCD plate for 23” LCD Monitor
310 Monitor Arm (Ergotron) - 23" KTZ304089 Monitor Arm (Ergotron) for 23” LCD Monitor 1 N Y
LCD
311 Monitor Cable Set MDT20 KTZ303952 MDT20 Monitor Cable Set for 23” LCD Monitor (1x Cable 1 N Y
USB3.0, 1x Cable DVI to HDMI, 1x Mini DIN Monitor
Power Cable)
312 Monitor Cable USB3.0 KTZ304034 MDT20 Monitor Cable USB3.0 (2 pcs.) 2 N Y
MDT20
403 Fuse Set KTZ280043 Fuses for Power Supply (T1.25A, T1.6A, T10A and T15A; - Y Y
10 pcs. each = 40)
503 RTF300-EC300 Probe KTZ303955 Probe Control Assembly ( Voluson E10, compatible to all 1 N Y
Control Board versions
504 RTF340-EC320 Probe KTZ304072 Probe Control Assembly ( Voluson E6 and Voluson E8 1 N Y
Control Board
505 RTF441-EC320 Probe KTZ304082 Probe Control Assembly ( compatible to all versions 1 N Y
Control Board
511 RSX10 - Extension Board for KTZ303250 Extension Board for FE-Mainboard RFM 1 N Y
RFM
512 RSX110 - Extension Board KTZ303759 Extension Board for FE-Mainboard RFM (Voluson E6 only 1 N Y
for RFM
513 RSX20 - Extension Board for KTZ303054 Extension Board for FE-Mainboard RFM + CW-steerable 1 N Y
RFM + CW-steerable
514 RSX120 - Extension Board KTZ303760 Extension Board for FE-Mainboard RFM + CW-steerable 1 N Y
for RFM + CW-steerable (Voluson E6 only
554 Battery Lithium CR2032 (3V) KTZ208791 Lithium Battery CR2032 (3V) for PC-Motherboard 1 N Y
555 Hard Disk Drive (HDD) KTZ302446 Hard disk drive SATA 500 Gbyte (Western Digital or 1 N Y
Hitachi) System/Boot DVD (see: Table 9-8 on page 9-
28 ) is required
556 Fan Set (2 fan) for PC - KTZ134698 Fan for PC-box (2 fan) - BackEnd 1 N Y
BackEnd
557 Back End Processor (BEP) KTZ303830 Kit contains ATX Motherboard "ADVANTECH", CPU 1 N Y
Kit, EC300 (BT15/BT16), incl. cooler, RAM, Fan(s), housing + internal cables
housing and cables premounted
558 Back End Processor (BEP) KTZ304075 Kit contains ATX Motherboard "ADVANTECH", CPU 1 N Y
Kit, EC320 (BT17), incl. cooler, RAM, Fan(s), housing + internal cables
housing and cables premounted
559 Back End Processor (BEP) KTZ304107 Kit contains Motherboard, CPU cooler, RAM, Fan(s), 1 N Y
Kit, EC330 (BT18), incl. housing + internal cables premounted
housing and cables
560 PC-Cover plate for GES35 KTZ304108 PC-Cover plate for GES35 (I/O panel and Video 1 N Y
Converter Board)
563 GES30 - External I/O KTZ303754 External Rear Panel incl. VGA, USB, Network and S- 1 N Y
Connection Panel Video cables to the Voluson E-Series system (internal)
564 GES35 - I/O Panel and Video KTZ304105 External I/O Panel and Video Converter Board (RTV35) 1 N Y
Converter Board (RTV35) incl. HDMI, VGA, USB, Network and S-Video connector
601 System/Boot DVD EC330 KTZ304119 bootable DVD for System HDD recovery 1 Y Y
(BT18 - Ext.0, 18.0.0) Contents: SP with newest MS patches, Linux rescue
partition, System C: Image (Windows 10), UISApp,
Backup, EUM, Database Repair Tool, etc.
Note: Refer to SN79009, which is the best source for the
latest revision.
602 System/Boot DVD EC320 KTZ304109 bootable DVD for System HDD recovery 1 Y Y
(BT17 - Ext.4, 17.0.4) Contents: SP with newest MS patches, Linux rescue
System/Boot DVD EC320 KTZ304100 partition, System C: Image (Windows 7), UISApp,
(BT17 - Ext.3, 17.0.3) Backup, EUM, Database Repair Tool, etc.
Note: Refer to SN79009, which is the best source for the
System/Boot DVD EC320 KTZ304094 latest revision.
(BT17 - Ext.2, 17.0.2)
603 System/Boot DVD EC310 KTZ304095 bootable DVD for System HDD recovery 1 Y Y
(BT16 - Ext.2, 16.0.3) Contents: SP with newest MS patches, Linux rescue
System/Boot DVD EC310 KTZ304084 partition, System C: Image (Windows 7), UISApp,
(BT16 - Ext.2, 16.0.2) Backup, EUM, Database Repair Tool, etc.
Note: Refer to SN79009, which is the best source for the
System/Boot DVD EC310 KTZ304066 latest revision.
(BT16 - Ext.1, 16.0.1)
604 System/Boot DVD EC300 KTZ304085 bootable DVD for System HDD recovery 1 Y Y
(BT15 - Ext.6, 15.0.6) Contents: SP with newest MS patches, Linux rescue
System/Boot DVD EC300 KTZ304067 partition, System C: Image (Windows 7), UISApp,
(BT15 - Ext.5, 15.0.5) Backup, EUM, Database Repair Tool, etc.
Note: Refer to SN79009, which is the best source for the
System/Boot DVD EC300 KTZ304056 latest revision.
(BT15 - Ext.4, 15.0.4)
605 Upgrade Kit: Voluson E- H48691ZG BT16 Upgrade kit (incl. System DVD, System Manuals, - N N
Series BT15 to BT16 etc.)
606 Upgrade Kit: Voluson E- H48701MS BT17 Upgrade kit (incl. Hardware components, System - N N
Series BT15 to BT17 DVD, System Manuals, etc.)
607 Upgrade Kit: Voluson E- H48701GW BT17 Upgrade kit (incl. Hardware components, System - N N
Series BT16 to BT17 DVD, System Manuals, etc.)
608 Upgrade Kit: Voluson E- H48701WC BT18 Upgrade kit (incl. Hardware components, System - N N
Series BT17 to BT18 DVD, System Manuals, etc.)
609 Upgrade Kit: Voluson E10 H48701EC OLED Monitor Upgrade kit (incl. Monitor OLED 22" - N N
OLED Monitor MDM300, Monitor Arm for OLED, Upgrade Manual)
613 Advanced VCI - Volume H48681FP encrypted Software Option string (password) - N N
Contrast Imaging
614 STIC “Basic” - Spatio- H48681FS encrypted Software Option string (password) - N N
Temporal Image Correlation
615 Coded Contrast Imaging - H48681FT encrypted Software Option string (password) - N N
Contrast Media
617 SonoAVC - Sono Automated H48681FX encrypted Software Option string (password) - N N
Volume Count
620 Advanced STIC * - Spatio- H48681GD encrypted Software Option string (password) - N N
Temporal Image Correlation
623 HDLive (Europe and Latin H48691KK encrypted Software Option string (password) - N N
America only)
624 HDLive Silhouette (BT15- H48691XZ encrypted Software Option string (password) - N N
BT17)
628 IOTA Simple Rules H48701WP encrypted Software Option string (password) - N N
629 eM6C (Electronic 4D Probe) H48691YA encrypted Software Option string (password) - N N
E4D Advanced Features
630 Full Disk Encryption H48701UX encrypted Software Option string (password) - N N
631 Advanced Security Features H48701WM encrypted Software Option string (password) - N N
632 SW DVR (Software Digital H48691XF encrypted Software Option string (password) - N N
Video Recorder)
633 DVD and USB Recorder H48701WR encrypted Software Option string (password) - N N
634 RLS Option (Russian H48691KG encrypted Software Option string (password) - N N
Language Support)
635 4D View Package (PC H48691KL encrypted Software Option string (password) - N N
software)
636 Swedish Key Cap Kit KTZ303956 kit includes special native language keys - Y Y
637 Danish Key Cap Kit KTZ303957 kit includes special native language keys - Y Y
638 Norwegian Key Cap Kit KTZ303958 kit includes special native language keys - Y Y
639 Finnish Key Cap Kit KTZ303959 kit includes special native language keys - Y Y
640 Spanish Key Cap Kit KTZ303960 kit includes special native language keys - Y Y
641 French Key Cap Kit KTZ303961 kit includes special native language keys - Y Y
642 German Key Cap Kit KTZ303962 kit includes special native language keys - Y Y
643 Italian Key Cap Kit KTZ303963 kit includes special native language keys - Y Y
644 Russian Key Cap Kit KTZ303964 kit includes special native language keys - Y Y
645 Swiss Key Cap Kit KTZ304060 kit includes special native language keys - Y Y
646 South Slavic Key Cap Kit KTZ304086 kit includes special native language keys - Y Y
Note For more detailed description of Software options and their functions, see: Section 5.1.4 "Description of
Software Options" on page 5-12 .
Note Not every feature is released in every country. Please contact Sales & Marketing in your region for
information on feature availability.
701 SATA Data Cable for HD- KTZ300244 SATA Data Cable for HD-Drive 1 N Y
Drive
702 PCI-E Connection Cable KTZ303121 PCI-E Connection from FrontEnd to BackEnd Cable 1 N Y
(FEP - BEP)
703 Cable Stereo Jack - Cinch KTZ280285 Cable from PC-Sound-StereoJack to DVD Shelf 2 N Y
RoHS
704 KVX1 Network Cable - RoHS KTZ280284 Network Cable from external rear panel (GES) to the 1 N Y
Voluson E-Series (internal) rear panel
705 Cable DVI (M) to HDMI (M) KTZ303895 Cable DVI (M) to HDMI (M), 30 cm 1 N Y
706 Cable HDMI (M) to HDMI (M) KTZ304110 Cable HDMI (M) to HDMI (M) 1 N Y
707 Monitor Cable Set MDT20 KTZ303952 MDT20 Monitor Cable Set for 23” LCD Monitor (1x Cable 1 N Y
USB3.0, 1x Cable DVI to HDMI, 1x Mini DIN Monitor
Power Cable)
708 Monitor Cable USB3.0 KTZ304034 MDT20 Monitor Cable USB3.0 (2 pcs.) 2 N Y
MDT20
709 Power Cord - Europe 230V KTZ220388 Power Cord Europe 230V/240V used at Mains Input - Y Y
Connector C14 (10A type)
710 Power Cord - USA (Hops. KTZ220389 Power Cord USA Hospital Grade used at Mains Input - Y Y
grade) Connector C14 (10A type)
711 Power Cord - Japan (Hops. KTZ220390 Power Cord Japan Hospital Grade used at Mains Input - Y Y
grade) Connector C14 (10A type)
712 Power Cord - China KTZ220391 Power Cord China used at Mains Input Connector C14 - Y Y
(10A type)
713 Power Cord - Australia KTZ220392 Power Cord Australia used at Mains Input Connector C14 - Y Y
(10A type)
714 Power Cord - India RoHS KTZ280289 Power Cord India used at Mains Input Connector C14 - Y Y
(10A type)
715 Power Cord - United KTZ220476 Power Cord United Kingdom (UK) 240V used at Mains - Y Y
Kingdom (UK) Input Connector C14 (10A type)
716 Power Cord - South Africa KTZ220477 Power Cord South Africa used at Mains Input Connector - Y Y
C14 (10A type)
717 Power Cord - Argentina KTZ220478 Power Cord Argentina used at Mains Input Connector - Y Y
C14 (10A type)
718 Power Cord - Israel KTZ220479 Power Cord Israel used at Mains Input Connector C14 - Y Y
(10A type)
719 Power Cord - Switzerland KTZ220480 Power Cord Switzerland used at Mains Input Connector - Y Y
C14 (10A type)
720 Power Cord - Denmark KTZ220481 Power Cord Denmark used at Mains Input Connector C14 - Y Y
(10A type) 2 pcs.
721 Power Cord - Brazil KTZ280185 Power Cord Brazil used at Mains Input Connector C14 - Y Y
(10A type)
722 Power Cord - Extension KTZ301990 Power Cord Extension for C13 connector (2m) - Y Y
723 Console Cable Set RTU100 KTZ303943 Console Cable Set RTU100 1 N Y
1 cable LVDS
2 cable Backplane -> Display
3 cable USB-A -> USB-mini
4 cable Main <-> Satellite
5 cable Main -> Backplane
6 cable USB-A <-> USB-B, white
7 cable USB-A <-> USB-B, black
8 cable UI main power D-SUB
9 cable Trackball
10 cable earth connection, 50mm
11 cable Frontkey <-> Main
12 cable USB Main PCB <-> AN PCB (USB)
13 cable Main -> Light
14 cable Display/Joycoder PCBA -> Main (JST PA)
15 cable earth connection, 100mm
724 USB3.0 Cable RTU100 KTZ304048 Cable USB3.0 (from RTH50 to external USB connectors 2 N Y
beside DVD Drive at Top Console) 2 pcs.
725 GES30 External I/O KTZ303754 External Rear Panel incl. VGA, USB, Network and S- 1 N Y
Connection Panel Video cables to the Voluson E-Series system (internal)
726 Cable Harness 3 EC3xx KTZ304077 Cable Harness 3 (Grounding, Console, Monitor DVI, 1 N Y
USB3.0, USB UI and USB Hub cable), cable tube, tie-
wraps, etc.
727 2nd HDD Power Cable KTZ280126 S-ATA Power Y-splitter cable for data transfer from old to - N Y
new HDD
728 SATA Data Cable for DVD- KTZ303261 SATA Data cable for DVD-Drive 1 N Y
Drive
729 SATA Power Cable for DVD- KTZ303260 SATA Power cable for DVD-Drive 1 N Y
Drive Note: Only used when RTH6x is installed.
730 USB Cable for ECG module KTZ303296 USB cable for ECG module 1 N Y
731 ECG patient cable KTZ303297 ECG patient cable, IEC Type - Y Y
9.10.1 Printers
Table 9-10 Optional Peripherals and Accessories - Printers
811 Digital BW Video Printer (e.g., KTZ220507 Digital B/W Video Printer, USB-Port - N Y
Sony UP-D898MD) H48651ML
812 Digital Color Printer ( Sony 5389822 Digital Color Printer, A6, USB-Port - N Y
UP-D25MD) H46831B
813 DeskJet Color Printer KTZ300182 DeskJet Color Line Printer Bluetooth incl. Ink, Bluetooth - N Y
Bluetooth (HP Officejet 100) H48661MT Adapter(s) + power cable US and EU
814 Printer Box Extension (for KTZ303932 Additional Printer Box for Color Printer A6, incl. mounting - N N
Color Printer) H48691WX plates and screws
815 Color Laser Printer (HP 5456780 Color Laser Printer for 220V systems - N Y
LaserJet M451) H48701EZ
816 Color Laser Printer (HP 5438549 Color Laser Printer for 110V systems - N Y
LaserJet M451) H48701FA
817 Color Laser Printer (HP 066E8922 Color Laser Printer for 220V systems - N Y
LaserJet M452dn)
818 Color Laser Printer (HP 066E8923 Color Laser Printer for 110V systems - N Y
LaserJet M452dn)
821 LAN Optical Isolation Box EP200132 LAN Patient Isolation Box - N Y
H45021EC
823 Cellular Modem KTZ304025 Cellular Modem (SIM Card Connection) incl. power supply - N Y
H48691WL and USB cable
825 Wireless Network Interface KTZ196269 Wireless Network Interface (“Netgear” WG111v3 WLAN - Y Y
H48671DT Adapter)
obsolete, please order PNo 5737413 except for systems
located in Brazil and (South)Korea
829 ECG-preamplifier (MAN30) KTZ304009 consists of ECG-preamplifier and patient connection cable - N Y
H48691LN
830 ECG patient cable KTZ303297 ECG patient cable, IEC Type - Y Y
831 Isolation Transformer kit H48671WN Isolation Transformer kit for Secondary Monitor incl. - - N
power cord set for US, EU and ROW (rest of world),
monitor power cable, fuses, documentation, etc.
833 Fuses for Isolation KTZ196333 Fuses for Isolation Transformer (2AT, 4AT; 10 pcs. each - Y Y
Transformer = 20)
834 RIC-Holder KTZ225469 Probe holder used for Real-time 4D endocavity probes - Y Y
(RIC) during disinfection process
836 UPS (Uninterruptible Power H48691PD Medical-grade UPS protection with built-in line-interactive - - N
Supply) for 100-130V AC voltage regulation (corrects brownouts as low as 82V and
countries overvoltages as high as 142V back to normal 120V
levels).
837 UPS (Uninterruptible Power H48691PE Medical-grade UPS protection with built-in line-interactive - - N
Supply) for 220-240V AC voltage regulation (corrects brownouts as low as 155V
countries and overvoltages as high as 274V back to normal 230V
levels).
838 Power Filter KTZ304093 Power Filter to eliminate EMC noise (filter incl. cables) - - N
H48701EL
839 VET-Label-Kit KTZ304117 Lables for Veterinay systems (Veterinary Use label 1 pcs., - - Y
H48701WX Not for Human Use label 1 pcs., VET label 2 pcs.)
Service Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
User Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
Service Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
User Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
Service Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
User Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
Service Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
User Manuals
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
Part Name Part No. - Voluson E8 Part No. - Voluson E6 Part No. - Voluson E10
9.12 Probes
Content in this section
9.12.1 2D-Probes - Curved Array Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-49
9.12.2 2D-Probes - Linear Array Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-51
9.12.3 2D-Probes - Phased Array Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-52
9.12.4 Real-Time 4D Volume Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-53
9.12.5 CW-Doppler - Pencil Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-56
Note Please observe that some probes are not applicable on all Voluson E-Series systems (depending on system
type and/or configuration).
900 4C-D 5162351 broadband curved array transducer, 2.0 - 5.0 MHz, 128 - Y Y
H4001BC Elements Applications: Abdominal, Obstetrics,
Gynecology
901 C1-5-D 5304539 broadband curved array transducer, 2.0 - 5.0 MHz, 192 - Y Y
H40452LE Elements Applications: Abdominal, Obstetrics,
Gynecology, Fetal Cardio
903 C4-8-D 5336339 broadband curved array transducer, 2.0 - 8.0 MHz, 192 - Y Y
H48681AS Elements Applications: Abdominal, Obstetrics,
Gynecology, Fetal Cardio, Pediatrics
904 IC5-9-D 5212417 endocavity broadband curved array transducer, 4.0 - 9.0 - Y Y
H40442LK MHz, 192 Elements, field of view: max. 175° Applications:
Obstetrics, Gynecology, Urology
910 11L-D 5410800 broadband linear array transducer, 4.0 - 10.0 MHz, 192 - Y Y
H40432LN Elements, electronically steerable Applications: Small
Parts, Peripheral Vascular, Pediatrics, Orthopedics
911 9L-D 5499510 broadband linear array transducer, 3.0 - 8.0 MHz, 192 - Y Y
H40442LM Elements, electronically steerable Applications: Small
Parts, Peripheral Vascular, Pediatrics, Orthopedics
912 ML6-15D 5271060 1,25D Matrix linear array transducer, 4.0 - 13.0 MHz, 336 - Y Y
H40452LG Elements / 3 rows (= 1008) Applications: Small-Part
(Breast), Peripheral Vascular, Pediatrics, Orthopedics
(Musculoskeletal), Neonatal, Urology
920 3SP-D KTZ280293 broadband phased array transducer, 1.0 - 5.0 MHz, 64 - Y Y
H48681AZ Elements Applications: Abdominal, Obstetrics,
Cardiology, Pediatrics, Neurology
921 S4-10-D 5394804 broadband phased array transducer, 4.0 - 9.0 MHz, 128 - Y Y
H45302LA Elements Applications: Small Parts, Cardiology,
Pediatrics
922 M5Sc-D 5446030 Matrix Single crystal phased array transducer, 1.5 - 4.6 - Y Y
H44901AE MHz, 80 Elements / 3 rows (= 270) Applications:
Obstetrics, Cardiology, Fetal Cardio, Pediatrics, Cephalic
934 eM6C G2* KTZ304083 1,5D Abdominal Matrix Array Real-time 4D broadband - Y Y
H48701ES electronic transducer, 128 azimuthal x 64 elevation
elements (= 8192) Applications: Abdominal Obstetrics,
Gynecology/Fertility, Pediatrics
Note Probes marked with an asterisk (*) are not applicable at Voluson E6 systems.
Note The Electronic Matrix probe "eM6C" is only applicable at Voluson E10 systems.
The probe RNA5-9-D is not applicable at Voluson E-Series BT16 (EC310, SW 16.x.x), BT17 (EC320, SW
17.x.x) and BT18 (EC330, SW 18.x.x) systems.
945 P2D KTZ280051 Continuous Wave (CW) Doppler pencil probe with a - Y Y
H4830JE center frequency of 2.0 MHz (no B-image), 2 Elements
Applications: Cardiology (suprasternal), Peripheral
Vascular, Neurology
946 P6D KTZ280050 Continuous Wave (CW) Doppler pencil probe with a - Y Y
H4830JG center frequency of 6.0 MHz (no B-image), 2 Elements
Applications: Cardiology, Peripheral Vascular, Pediatrics
CW-Doppler Pencil Probes are not applicable at Voluson E-Series BT16 (EC310, SW 16.x.x), BT17 (EC320,
SW 17.x.x) and BT18 (EC330, SW 18.x.x) systems.
950 ****** E8385MJ disposable Biopsy needle guide for probe IC5-9-D needle - - N
(disposable) diameter: 16-18GA (gauge); 1.2 - 1.6 mm
951 ****** H40412LN reusable Biopsy needle guide for probe IC5-9-D needle - - N
(reusable) diameter: < 1.65 mm
952 PEC63 H46721R reusable Biopsy needle guide for probe RIC5-9-D / - - N
RIC6-12-D needle diameter: < 1.8 mm
953 RIC Single-angle bracket H48681GF disposable Biopsy needle guide for probe RIC5-9-D / - - N
RIC6-12-D needle diameter: 16-18GA (gauge); 1.2 - 1.6
954 RIC Single-angle bracket + H48691Z mm - - N
Latex Cover
955 PEC74 H48621Y reusable Biopsy needle guide for probe RAB2-5-D needle - - N
diameter: < 1 mm, 1.4 mm, 2.2 mm
956 RAB Single-angle bracket H46701AE Non Sterile Single Angle Bracket needle guide for probe - - N
RAB2-5-D needle diameter: 8.5FR, 14-23GA (gauge); >
0.6 mm - < 2.1 mm
957 eM6C Biopsy Starter Kit H48681MK Biopsy Starter Kit for Matrix probe eM6C needle diameter: - - N
8.5FR, 14-23GA (gauge); > 0.6 mm - < 2.1 mm
958 eM6C G2 Biopsy Starter Kit H48701MP Biopsy Starter Kit for Matrix probe eM6C G2 needle - - N
diameter: 8.5FR, 14-23GA (gauge); > 0.6 mm - < 2.1 mm
959 PEC75 H46721W reusable Biopsy needle guide for probe RSP6-16-D - - N
needle diameter: < 1 mm, 1.4 mm, 2.2 mm
960 RSP Single-angle bracket H46701AD Non Sterile Single Angle Bracket needle guide for probe - - N
RSP6-16-D needle diameter: 8.5FR, 14-23GA (gauge); >
0.6 mm - < 2.1 mm
961 PEC76 H48651DG reusable Biopsy needle guide for probe RNA5-9-D needle - - N
diameter: < 1 mm, 1.4 mm, 2.2 mm
962 RNA Single-angle bracket H46701AF Non Sterile Single Angle Bracket needle guide for probe - - N
RNA5-9-D needle diameter: 8.5FR, 14-23GA (gauge); >
0.6 mm - < 2.1 mm
963 RAB6 Biopsy Starter Kit H48681ML Biopsy Starter Kit for UltraLight probe RAB6-D needle - - N
diameter: 8.5FR, 14-23GA (gauge); > 0.6 mm - < 2.1 mm
964 4C Multi-angle bracket E8385NA Non Sterile Multi Angle Bracket needle guide starter kit for - - N
probe 4C-D needle diameter: 8.5FR, 14-23GA (gauge); >
0.6 mm - < 2.1 mm
965 C1-5-D Biopsy guide H40432LE Non Sterile Multi Angle Bracket needle guide for probe - - N
C1-5-D needle diameter: 8.5FR, 14-23GA (gauge); > 0.6
mm - < 2.1 mm
966 C2-9-D Biopsy guide H4913BA Non Sterile Multi Angle Bracket needle guide for probe - - N
C2-9-D needle diameter: 8.5FR, 14-23GA (gauge); > 0.6
mm - < 2.1 mm
967 C4-8-D Biopsy guide H48681AT Non Sterile Multi Angle Bracket needle guide for probe - - N
C4-8-D needle diameter: 8.5FR, 14-23GA (gauge); > 0.6
mm - < 2.1 mm
968 12L-RS Multi-angle bracket H40432LC Non Sterile Multi Angle Bracket needle guide for probe - - N
11L-D needle diameter: 8.5FR, 14-23GA (gauge); > 0.6
mm - < 2.1 mm
969 9L Multi-angle bracket H4906BK Non Sterile Multi Angle Bracket needle guide for probe - - N
9L-D needle diameter: 8.5FR, 14-23GA (gauge); > 0.6
mm - < 2.1 mm
970 ML6-15D Biopsy kit H40432LJ Non Sterile Multi Angle Bracket needle guide for probe - - N
ML6-15-D needle diameter: 8.5FR, 14-23GA (gauge); >
0.6 mm - < 2.1 mm
971 3SP Multi-angle bracket H46222LC Non Sterile Multi Angle Bracket needle guide for probe - - N
3SP-D needle diameter: 8.5FR, 14-23GA (gauge); > 0.6
mm - < 2.1 mm
972 M5S-D Multi-angle bracket H45561FC Non Sterile Multi Angle Bracket needle guide for probe - - N
M5Sc-D needle diameter: 8.5FR, 14-23GA (gauge); > 0.6
mm - < 2.1 mm
This chapter describes Care and Maintenance on the Voluson E-Series system
and its peripherals. These procedures are intended to maintain the quality of the
Voluson E-Series systems performance. Read this chapter completely and
familiarize yourself with the procedures before performing a task.
Warning
Be sure to disconnect the Voluson E-Series ultrasound system power plug and switch off the main
circuit breaker before you remove any parts. Be cautious whenever power is still on and covers are
removed.
Caution
Do not pull out or insert circuit boards while power is ON.
Caution
The system requires all covers. Do not operate the Voluson E-Series system unless all board
covers and frame panels are securely in place. The covers are required for safe operation, good
system performance and cooling purposes. When covers are removed, EMI may be present.
Caution
To ensure the mutual protection and safety of GE service personnel and our customers, all
equipment and work areas must be clean and free of any hazardous contaminants before a service
engineer starts a repair. This includes, but is not limited to, decontamination and/or sterilization,
depending on the application or use of the medical device.
It has been determined by engineering that your Voluson E-Series system does not have any high wear
components that fail with use, therefore no Periodic Maintenance Inspections are mandatory. However,
some Customers Quality Assurance Programs may require additional tasks and/or inspections at a different
frequency than listed in this manual.
It is good business practice that ultrasound facilities maintain records of periodic and corrective
maintenance. The Ultrasound Equipment Quality Check form provides the customer with documentation that
the ultrasound system is maintained on a periodic basis.
A copy of the Ultrasound Equipment Quality Check form should be kept in the same room or near the
Voluson E-Series ultrasound system.
In order to gain accreditation from organizations such as the American College of Radiology (USA), it is the
customer's responsibility to have a quality assurance program in place for each system. The program must
be directed by a medical physicist, the supervising radiologist/physician or an appropriate designee.
Routine quality control testing must occur regularly. The same tests are performed during each period so
that changes can be monitored over time and effective corrective action can be taken.
Testing results, corrective action and the effects of corrective action must be documented and maintained on
the site.
Your GE service representative can help you with establishing, performing and maintaining records for a
quality assurance program. Please contact us for coverage information and/or price for service.
The Customer Care Schedule (see: Table 10-1 on page 10-3 ) specifies how often your Voluson E-Series
should be serviced and outlines items requiring special attention.
Note It is the customer's responsibility to ensure that the Voluson E-Series care & maintenance is performed as
scheduled in order to retain its high level of safety, dependability and performance.
Your GE Service Representative has an in-depth knowledge of your Voluson E-Series ultrasound system
and can best provide competent, efficient service. Contact GE for coverage information and/or price for
service.
The service procedures and recommended intervals shown in the Customer Care Schedule assumes that
you use your Voluson E-Series for an average patient load (10 per day) and not use it as a primary mobile
system which is transported between diagnostic facilities.
Note If conditions exist which exceed typical usage and patient load, then it is recommended to increase the
maintenance frequencies.
Abbreviations used in the Customer Care Schedule Table 10-1:
• D = Daily
• W = Weekly
• M = Monthly
• A = Annually
Air Filter Grid Remove the filter grid and clean the air filter grid with • more frequently depending on your
vacuum cleaner from outside. environment
Air Filter Grid Remove filter grid, back top cover and back cover and • more frequently depending on your
clean the housing from inside. (vacuum cleaner and environment
soft brush)
Cables and Connectors Check if all cables are fixed and well seated at the • also after corrective maintenance
correct position and if there is no mechanical damage
visible.
User Interface Clean alphanumerical keyboard, functional keys, • Be careful not to get the cloth too wet
digital potentiometers. (vacuum cleaner, lukewarm so that moisture does not enter the
soap water on a soft, damp cloth) loudspeakers or other keys!
LCD Monitor, Touch Clean LCD monitor surface, Touch Panel and probe • Be careful not to get the cloth too wet
Panel and Probe holder holder with a fluid detergent in warm water on a soft, so that moisture does not enter the
damp cloth. entire system.
Mechanical parts Clean and inspect the mechanical function of wheels, • mobile systems check daily
casters, brakes and swivel locks as well as side door,
foot rest, front and rear handle, and monitor holder.
Remove dust and coupling gel.
Control Console Check translation/rotation and height adjustment • more frequently at mobile systems
movement (elevation)
Trackball Check Check proper operation (cursor movement X, Y • If failure occurs go to trackball
direction) cleaning.
Trackball Cleaning Remove trackball ring; open the trackball housing and •
take out the trackball (see Section 7.8.3 on page 7-
25 ). Clean the trackball (and X,Y axes) with soft
tissue and screwdriver shaft.
Disk Drives (Data Test image filing (Archive) import and export data • •* * save the image filing data weekly or
Backup) capability (DVD/CD Drive) at least monthly on DVD/CD
depending on the number of
examinations
Safe Probe Operation Clean probes and probe cables and check acoustic •* * or before each use
lens housing (cracks) and probe cables. In case of
mechanical damage, don't use them! Danger: Safety
risk for operator and patient.
Probe Air bubbles To detect air bubbles in filling liquid, shake the probe
carefully and check for abnormal noise.
Probe/Phantom Checks Check gain changes, vary the focus and check • Also after corrective maintenance or
reaction on screen. as required by your facilities QA
NOTE! The use of a Phantom is not required during program.
Preventive Maintenance. Customer may use it as part
of their Quality Assurance Program tests.
Note Electrical leakage testing may be accomplished with any calibrated Electrical Safety Analyzer tool compliant
with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551 or IEC 62353 or other relevant national regulation.
Tools Comments
Digital Volt Meter (DVM) minimum 5% accuracy, 3.5 digit and 200 Ohm range required
Anti Static Kit including anti-static mat, wrist strap, cables and conductive ground cord
QIQ Phantom NOTE! The use of a Phantom is not required during Preventive Maintenance. Customer
may use it as part of their Quality Assurance Program tests.
B/W Printer Cleaning Sheet see printer user manual for requirements
Color Printer Cleaning Sheet see printer user manual for requirements
Disposable Cloves •
The preliminary checks take about 15 minutes to perform. Refer to the Voluson E-Series user documentation
whenever necessary.
1 Ask and Listen Ask the customer if they have any problems or questions about the equipment.
2 Power up • Turn the system power on and verify that all fans and peripherals turn on.
• Watch the displays during power up to verify that no warning or error messages are displayed.
3 Probes Verify that the ultrasound system properly recognizes all probes.
4 Displays Verify proper display on the LCD monitor and Touch Panel (when present).
5 Presets “Full Backup” all customer presets onto appropriate media (see: Section 4.4.3 "Save Full System
Configuration (Full Backup)" on page 4-15 ).
6 Image Archive Backup the Image Archive onto appropriate media (see: Section 4.4.6.1 "Save Image Archive" on
page 4-20 ).
The functional checks take about 60 minutes to perform. Refer to the Voluson E-Series user documentation
whenever necessary.
1 B Mode Verify basic B Mode (2D) operation. Check the basic ultrasound system controls that affect this mode
of operation.
2 M Mode Verify basic M Mode operation. Check the basic ultrasound system controls that affect this mode of
operation.
3 C Mode Verify basic CFM Mode (Color Flow Mode) operation. Check the basic ultrasound system controls that
affect this mode of operation.
4 PD Mode Verify basic PD Mode (Power Doppler Mode) operation. Check the basic ultrasound system controls
that affect this mode of operation.
5 Doppler Modes Verify basic Doppler Mode operation (PW and CW if available). Check the basic ultrasound system
controls that affect this mode of operation.
6 3D Mode Verify basic 3D Mode operation. Check the basic ultrasound system controls that affect this mode of
operation.
7 RealTime 4D Mode Verify basic RealTime 4D Mode operation. Check the basic ultrasound system controls that affect this
(optional) mode of operation.
8 *Applicable Verify the basic operation of all optional modes. Check the basic system controls that affect each
Software Options option`s operation.
9 Keyboard Test Perform the Keyboard Test Procedure to verify that all keyboard controls are OK.
Note * Some software may be considered standard depending upon system model configuration.
2 B/W Printer Verify hardcopy output of the B/W video page printer. Clean heads and covers if necessary.
3 Color Printer Verify hardcopy output of the Color video page printer. Clean heads and covers if necessary.
4 Color Deskjet Verify hardcopy output of the Deskjet (Bluetooth) printer. Clean heads and covers if necessary.
(Bluetooth) Printer
5 DICOM Verify that DICOM is functioning properly. Send an image to a DICOM device.
1 Unplug Cord Disconnect the mains cable from the wall and ultrasound system.
3 Verify Verify that the LINE, NEUTRAL and GROUND wires are properly attached to the terminals, and that
no strands may cause a short circuit.
1 Labeling Verify that all ultrasound system labeling is present and in readable condition.
2 Covers Where applicable, verify all covers are secured in place and are properly aligned with other covers.
Replace any covers that are damaged.
3 Control Console Inspect the control console and keyboard. Record any damaged or missing items. (Replace faulty
and Keyboard components, as required).
4 Control Console • Where applicable, verify ease of control console movement in all acceptable directions.
Movement • Where applicable, ensure that it latches in position as required.
6 LCD Monitor Inspect the LCD Display for scratches and bad pixels. Verify proper operation of Contrast and
Brightness controls. Where applicable, confirm that the LCD arm allows:
• swivelling the screen to the left and to the right
• folding the screen to the locked position
• release and adjustment backwards and forwards
• can be adjusted in the up/down positions
Note: LCD Arm movement may vary and is not applicable to all ultrasound systems.
7 Monitor Light Check for proper operation of any monitor lights, if available.
8 Cables and Check all internal cable harnesses and connectors for wear and secure connector seating. Pay
Connectors special attention to footswitch assembly and probe strain or bend reliefs.
9 Shielding & Covers Check to ensure that all EMI shielding, internal covers, air flow panels and screws are in place.
Missing covers and hardware could cause EMI/RFI problems during scanning.
10 Probe Holders Where applicable, inspect the Probe Holders for cracks or damage.
11 Power and System Check for proper operation of all Power and System Status Indicators.
Status Indicators
12 External I/O Check all connectors for damage and verify that the labeling is good.
13 Wheels and Brakes • Check all wheels and casters for wear and verify operation of foot brake, to stop the system from
moving, and release mechanism.
• Check all wheel locks and wheel swivel locks for proper operation.
14 Battery Where applicable, check that the battery is not damaged, does not leak, does not emit an odor, and is
not deformed or discolored. Observe all warnings and cautions for battery handling, recharging,
storing, and/or disposal.
10.4.4 Cleaning
The Basic User Manual of the Voluson E-Series system provides a complete description of system/probe
care, maintenance, cleaning and disinfection.
Note It is the responsibility of the user to decide which cleaning procedures are necessary to ensure a safe
working environment.
Warning
• Before cleaning the Voluson E-Series system switch it off and disconnect from AC mains.
• Electric parts must be protected from liquids that drip or seep into the system.
• Electrical contacts and connectors must not be cleaned.
• Do not use high-proof alcohol for cleaning. Only use cleaning/disinfecting agents listed in the Basic
User Manual of the Voluson E-Series system.
1 Console Use cleaning agent on a soft, non-abrasive, damp cloth to carefully wipe the entire system. Be careful
not to get the cloth too wet so that moisture does not enter the console. Caution: DO NOT allow any
liquid to drip or seep into the system.
2 LCD Monitor + Clean LCD Monitor surface and Touch Panel with cleaning agent on a soft, non-abrasive, damp cloth.
Touch Panel Caution: DO NOT spray any liquid directly onto Voluson E-Series covers, Monitor, keyboard, etc.
1 Probes Thoroughly check the ultrasound system probe connectors and remove dust from inside the connector
sockets if necessary. Visually check for bent, damaged or missing pins.
2 Probes Verify that the ultrasound system properly recognizes all probes.
3 Probe Holder Clean probe holders (they may need to be soaked to remove excess gel).
Caution
To help protect yourself from blood borne diseases, wear approved disposable gloves. These are made of
nitrile derived from vegetable starch to prevent allergic latex reactions.
Caution
Failure to follow the prescribed cleaning or disinfection procedures will void the probes warranty. Do not soak
or wipe the lens with any product not listed in the Voluson E-Series Basic User Manual and/or care card.
Doing so could result in irreparable damage to the probe.
Caution
Disinfect a defective probe before you return it. Be sure to tag the probe as being disinfected.
Caution
Follow the Care Card instructions supplied with each probe (inside the probe boxes) for disinfectants and
gels that are compatible with the surface material of the probes.
Note For the latest list of compatible cleaning solutions and disinfectants refer to: http://www.gehealthcare.com/
transducers.
Please be aware of the NEVER place or store a probe When disinfecting a probe,
sensitive probe head. TAKE on its scan head! ensure that there is sufficient
EXTREME CARE! space between the probe and
the container bottom!
Warning
Energy Control and Power Lockout for Voluson E-Series:
When servicing parts of the system where there is exposure to voltage greater than 30 Volts:
1. Follow LOTO (Lockout/Tagout) procedures.
2. Turn off the breaker.
3. Unplug the Voluson E-Series system.
4. Maintain control of the Voluson E-Series system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.
The electrical safety tests in this section are based on IEC60601 standard including national deviations for
Health Care Facilities and IEC 62353 Medical electrical equipment – Recurrent test and test after repair of
medical electrical equipment. These standards provide guidance on evaluating electrical safety of medical
devices which are placed into service and are intended for use in planned maintenance (PM) or testing
following service or repair activities. They differ somewhat from the standards that are used for design
verification and manufacturing tests (e.g., IEC 60601-1 including national deviations) which require a
controlled test environment and can place unnecessary stress on the ultrasound system.
These tests may refer to specific safety analyzer equipment as an example. Always refer to the safety
analyzer's user manual that will be used to perform the tests.
Prior to initiating any electrical test, the system must be visually inspected. Perform following visual checks:
• Check for missing or loose enclosure covers that could allow access to internal live parts.
• Examine the mains cord, mains plug and appliance inlet for damaged insulation and adequacy of strain
relief and cable clamps.
• Locate and examine all associated probes. Inspect the cables and strain relief at each end. Inspect the
probe enclosure and lens for cracks, holes and similar defects.
Caution
For all instructions in this section: In case of using an UPS (uninterruptable power supply) the terms outlet,
wall outlet, AC wall outlet or power outlet refer to the AC wall outlet to which the UPS power input is
connected to. In case of further available AC (or DC) power outlets at the same used UPS these must
remain unused; i.e. not connected to any other devices.
Warning
Users must ensure that safety inspections are performed whenever damage is suspected and on a regular
basis in accordance with local authorities and facility procedures. DO NOT use the Voluson E-Series system
or individual probes which fail any portion of the safety test.
Warning
To minimize the risk and to avoid an electric shock, only trained persons are allowed to perform the electric
safety inspections and tests.
Caution
Compare all safety-test results with safety-test results of previously performed safety tests (e.g., last year
ect). In case of unexplainable abrupt changes of safety-test results consult experienced authorized service
personnel or GE for further analysis.
Caution
To avoid electrical shock, the Voluson E-Series system under test must not be connected to other electrical
equipment. Remove all interconnecting cables and wires. The system under test must not be contacted by
users or patients while performing these tests.
The following acceptance limits and test conditions are summarized from IEC 60601 including national
deviations and IEC 62353 and in some cases are lower than that specified by the standards.
Type BF Applied Parts (sink leakage, On and Off Closed 5.0 5000
mains voltage on applied part)
* ISO and Mains Applied refers to the sink leakage test where mains (supply) voltage is applied to the
applied part to determine the amount of current that will pass (or sink) to ground if a patient is in contact with
mains voltage.
Note Electrical leakage testing may be accomplished with any calibrated Electrical Safety Analyzer tool compliant
with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551 or IEC 62353 or other relevant national regulation.
Applied Parts (AP) Parts or accessories that contact the patient to perform their function. For ultrasound equipment, this
includes transducers and ECG leads and e-TRAX Needle Sensor.
Type BF Type BF Applied Part (man in the box) symbol is in accordance with IEC 60417-5333.
e.g., ultrasound probes which are marked with the 'man in box' BF symbol
Type BF Type BF defibrillation proof Applied Part (man in the box with paddle) symbol is in
Defibrillator-proof accordance with IEC 60417-5334.
e.g., ECG electrodes which are marked with the 'man in box with paddle' BF symbol
Type CF Type CF Applied Part (heart in the box) symbol is in accordance with IEC 60417-5335.
e.g., intraoperative probes for direct cardiac contact, isolated ECG connections and e-TRAX
Needle Sensor, so marked with the 'heart in box' CF symbol
Type CF Type CF defibrillation proof Applied Part (heart in the box with paddle) symbol is in
Defibrillator-proof accordance with IEC 60417-5336.
e.g., intraoperative probes for direct cardiac contact, isolated ECG connections and e-TRAX
Needle Sensor, so marked with the 'heart in box with paddle' CF symbol
Sink Leakage The current resulting from the application of mains voltage to the applied part. This test is required for Type
BF and CF applied parts.
Test all outlets in the area for proper grounding and wiring arrangement by plugging in the neon outlet tester
and noting the combination of lights that are illuminated. Any problems found should be reported to the
hospital immediately and the receptacle should not be used.
Note No outlet tester can detect the condition where the Neutral (grounded supply) conductor and the Grounding
(protective earth) conductor are reversed. If later tests indicate high leakage currents, this should be
suspected as a possible cause and the outlet wiring should be visually inspected.
Measure the resistance from the third pin of the attachment plug to the exposed metal parts of the case. The
ground wire resistance should be less than 0.2 ohms. Reference the procedure in the IEC60601-1-1 and/or
IEC62353.
Caution
Lacquer is an isolation barrier! Measure only on blank accessible metal parts.
10.6.5.1 Definition
This test, also known as Enclosure Leakage current test, measures the current that would flow through a
grounded person who touches the accessible conductive parts of the equipment during normal and fault
conditions.
The test verifies the isolation of the power line from the chassis.
The meter is connected to parts of the equipment, easily contacted by the user or patient.
Record the highest reading.
Note For more information, refer to the safety analyzer's user manual that will be used to perform the test.
The maximum allowable limit for chassis source leakage is shown in:
• Table 10-10 on page 10-11 , as Chassis/Enclosure Leakage.
Follow the test conditions described for respective test points shown in the table below.
Table 10-14 Typical Data Format for recording Enclosure/Chassis Leakage Current
on closed 100
on open 500
10.6.6.1 Definition
This test measures the current which would flow to ground from any of the isolated ECG leads. The meter
simulates a patient who is connected to the monitoring equipment and is grounded by touching some other
grounded surface. Measurements should be made with the ground open and closed, with power line polarity
normal and reversed, and with the Voluson E-Series ultrasound system on and off.
For each combination the operating controls, such as the lead switch, should be operated to find the worst
case condition.
Note For more information, refer to the safety analyzer's user manual that will be used to perform the test.
Measurements should be made under the test conditions specified in:
• Table 10-10 on page 10-11 , as applicable.
For each combination, the operating controls, such as the lead switch, should be operated to find the worst
case condition.
Record all data and keep the record of the results with other hard copies of maintenance data.
6 AC wall outlet
Note For more information, refer to the safety analyzer's user manual that will be used to perform the test.
Table 10-15 Typical Data Format for recording Patient Lead to Lead Leakage
off closed 10
off open 50
on closed 10
on open 50
Select the ALL position on the LEAD selector since the test is performed with mains applied to all ECG leads
at the same time.
Caution
Line voltage is applied to the ECG leads during this test. To avoid possible electric shock hazard, the system
being tested must not be touched by patients, users or anyone while the ISO TEST switch is depressed.
Note For more information, refer to the safety analyzer's user manual that will be used to perform the test.
Table 10-16 Typical Data Format for recording Isolated Patient Lead (sink) Leakage
on closed 50
off closed 50
Warning
Do not use the probe if the insulating material has been punctured or otherwise compromised. Integrity of the
insulation material and patient safety can be verified by safety testing according to IEC60601-1.
10.6.9.1 Definition
This test measures the current that would flow to ground from any of the probes through a patient who is
being scanned and becomes grounded by touching some other grounded surface.
Note Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage
currents are normal from probe to probe. Other variations will result from differences in line voltage and test
lead placement. It is abnormal if no leakage current is measured. If no leakage current is detected, check the
configuration of the test equipment.
Note Saline water pod should be insulated from floor and earth ground.
The Saline solution is a mixture of water and salt. The salt adds free ions to the water, making it conductive.
Normal saline solution is 0.9% salt and 99.1% water. If ready-mixed saline solution is not available, a mixture
of 1 quart or 1 liter water with 9 or more grams of table salt, mixed thoroughly, will substitute.
Note Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage
currents are normal from probe to probe. Other variations will result from differences in line voltage and test
lead placement. It is abnormal if no leakage current is measured. If no leakage current is detected, check the
configuration of the test equipment.
The ultrasound probes imaging area is immersed in the Saline solution along with a grounding probe from
the test meter to complete the current path.
This test is also known as Patient Leakage Current.
1. Turn the Voluson E-Series system OFF.
2. Connect the Safety analyzer to an AC wall outlet.
3. Set the Safety analyzer's function switch to "Chassis" or "Enclosure Leakage".
4. Plug the Voluson E-Series system's power cord into the test meter.
5. Plug the Chassis Ground Probe (saline probe) into the test meter's “CHASSIS” connector.
6. Connect the ultrasound probe to be tested to the Voluson E-Series system.
7. Immerse the saline probe in the saline solution.
8. Immerse the Voluson E-Series probe´s face (imaging area of the probe) into the saline solution.
Caution
To avoid probe damage and possible electric shock, do not immerse probes into any liquid beyond the level
indicated shown below.
Do not touch the probe, conductive liquid or any part of the system under test while doing the test.
The actual location of the test probe may vary by system. Measurements should be recorded for each probe
under the set of test conditions.
Record all data and keep the record of the results with other hard copies of maintenance data.
Table 10-17 Typical Data Format for recording Probe (source) Leakage Current
on closed 100
on open 500
Caution
Line voltage is applied to the ultrasound probe during this test. To avoid possible electric shock hazard, the
system being tested must not be touched by patients, users or anyone while the ISO TEST switch is
depressed.
Measurements should be recorded for full lead combination under each set of test conditions specified in:
• Table 10-11 on page 10-11
Record all data and keep the record of the results with other hard copies of maintenance data.
1. Connect the Safety analyzer to an AC wall outlet.
2. Plug the equipment under test into the receptacle on the panel of the meter.
3. Connect the ultrasound probe to be tested to the Voluson E-Series system.
4. Immerse the saline probe in the saline solution.
5. Immerse the Voluson E-Series probe´s face (imaging area of the probe) into the saline solution.
6. Select the "Patient Lead Leakage" function on the meter.
7. Test with closed ground with the Voluson E-Series system on and off.
Note For more information, refer to the safety analyzer's user manual that will be used to perform the test.
Record all data and keep the record of the results with other hard copies of maintenance data.
Table 10-18 Typical Data Format for recording Isolated Probe (sink) Leakage
on closed 5000
Where applicable, check the AC/DC adapter and its cable. Replace a new one if any portion is defective.
Check the ground on the power cord and plug for continuity. Ensure the ground is not broken, frayed, or
intermittent. Replace any defective part.
Tighten all grounds. Ensure star washers are under all ground studs. Inspect wiring for bad crimps, poor
connections, or damage.
Test the wall outlet; verify it is grounded and free of other wiring abnormalities. Notify the user or owner to
correct any deviations. As a work around, check the other outlets to see if they could be used instead.
Note No outlet tester can detect the condition where the white neutral wire and the green grounding wire are
reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the
outlet wiring should be visually inspected. If reversed wiring is observed, it is the customers responsibility to
have the condition corrected by qualified personnel.
Test another probe to isolate if the fault lies with the probe or the system.
Note Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage
currents are normal from probe to probe. Other variations will result from differences in line voltage and test
lead placement. The maximum allowable leakage current for body surface contact probe differs from inter-
cavity probe. Be sure to enter the correct probe type in the appropriate space on the check list.
Test the probe in another connector to isolate if the fault lies with the probe or the system. If excessive
leakage current is slot dependent, inspect the system connector for bent pins, poor connections, and ground
continuity.
If the problem remains with the probe, replace the probe.
Tighten all grounds. Ensure star washers are under all ground studs.
Inspect wiring for bad crimps, poor connections, or damage.
If all else fails, begin isolation by removing the probes, external peripherals, then the on board ones, one at a
time while monitoring the leakage current measurement.
In case of using an UPS (Uninterruptible Power Supply), perform the tests in the “Electrical Safety tests”
section without using the UPS (i.e. directly connect the Voluson E-Series system to the AC wall outlet). If this
leads to a pass result, the specific UPS must no longer be used.
If the leakage current measurement tests fail on a new Voluson E-Series system and if situation can not be
corrected, submit a Safety Failure Report to document the problem. Remove Voluson E-Series system from
operation.