Vivid T8
Vivid T8
Technical Publication
Vivid™ T8/Vivid T8 Pro
Proprietary Service Manual
Direction Number: 5718825-100 English
Rev. 15
This manual is a reference for the Vivid T8, Vivid T8 Pro. It applies to all versions of
the R1.x.x, R2.x.x software for the Vivid T8 ultrasound system. It applies to all
versions of the R1.x.x software for the Vivid T8 Pro ultrasound system.
GE
DATE 3
REV (YYYY/MM/DD) REASON FOR CHANGE
Rev. 07 2017/10/10 Update flexible arm information and spare part list
REVISION REVISION
CHAPTER NUMBER NUMBER CHAPTER NUMBER NUMBER
Chapter 5 Rev. 15
Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop/ePDM (GE electronic Product
Data Management). If you need to know the latest revision, contact your distributor, local
GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at
1 800 682 5327 or 1 262 524 5698.
Translation policy
Proprietary to GE Healthcare
Permission to use this Advanced Service Software and related
documentation (herein called the material) by persons other
than GE Healthcare employees is provided only under an
Advanced Service Package License relating specifically to this
Proprietary Material. This is a different agreement from the one
under which operating and basic service software is licensed. A
license to use operating or basic service software does not
extend to or cover this software or related documentation.
If you are a GE Healthcare employee or a customer who has
entered into such a license agreement with GE Healthcare to
use this proprietary software, you are authorized to use this
Material according to the conditions stated in your license
agreement.
However, you do not have the permission of GE Healthcare to
alter, decompose or reverse-assemble the software, and unless
you are a GE employee, you may not copy the Material. The
Material is protected by Copyright and Trade Secret laws; the
violation of which can result in civil damages and criminal
prosecution.
If you are not party to such a license agreement or a GE
Healthcare Employee, you must exit this Material now.
Trademarks
All products and their name brands are trademarks of their
respective holders.
Copyrights
All Material Copyright © 2015-2023 by
General Electric Company Inc. All Rights Reserved.
Introduction
1-1 Overview
Category R1 Upgraded R2 R2
UDI Label NO The upgrade UDI label is on The UDI label is on the rating
the back cover. plate
OR
The part number on CPU is The part number on CPU is The part number on CPU is
5487374. 5717877. 5717877.
OR
Category R1 Upgraded R2 R2
Internal Box The part number on the label is 5495619-3 For R2.0.2 and below, the part
number on the label is
5495619-4
For R2.0.3 and above, the part
number on the label is
5495619-5
There is one connector in There is one connector in this For R2.0.2 and below, there are
this ___location. ___location. two connectors in this ___location.
The CPU in the box is The CPU in the box is 5717877 For R2.0.3 and above, there
5487374 are three connectors in this
___location.
Category R1 Upgraded R2 R2
1-3-1-2 Icons
ELECTRICAL
MECHANICAL
RADIATION
LASER
HEAT
PINCH
Table 1-5: Standard Icons that indicates that a special procedure is to be used
Avoid Static Electricity Tag and Lock Out Wear Eye Protection
NOTE: If the new label is needed during the service activities, please
click “Ask an Expert“ to submit the case in the support central:
http://supportcentral.ge.com/products/sup_products.asp?prod_
id=44177.
1-6-2 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.
WARNING Have two people available to deliver and unpack the Vivid T8/
Vivid T8 Pro.
Attempts to move the Ultrasound system considerable
distances or on an incline by one person could result in injury
or damage or both.
WARNING Ensure that the Ultrasound system is turned off and unplugged
Wait for at least 20 seconds for capacitors to discharge as
there are no test points to verify isolation. The amber light on
the OP panel ON/OFF button will turn off.
Ultrasound system components may be energized. Always
refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions
WARNING Never use a probe that has fallen to the floor. Even if it looks
OK, it may be damaged.
CAUTION To avoid injury when you move the LCD monitor and the
monitor arm, do not put your finger, hand, or object on the joint
of the monitor or the monitor arm.
CAUTION Ensure that nobody touches the console arm when moving the
operator panel.
CAUTION Use safety shoes when doing work where there is any chance
of foot injury.
CAUTION Use protective gloves when working with sharp edges or when
directed to wear PPE during a removal/replacement procedure.
1-6-5-2 Probes
1-6-5-3 Peripherals
WARNING Energy Control and Power Lockout for Vivid T8/Vivid T8 Pro.
When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.
1-9-1 Overview
Equipment being returned must be clean and free of blood and
other infectious substances. GE Healthcare policy states that
body fluids must be properly removed from any part or
equipment prior to shipment. GE Healthcare 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 an 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 that 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 purposes and must be transported as a
hazardous material.
1-9-1 Overview(continued)
NOTE: The USER/SERVICE staff should dispose of all the waste
properly, per federal, state, and local waste disposal regulations.
The Ultrasound 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.
1-10-2 CE Compliance
Vivid T8/Vivid T8 Pro 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.
For applicable standards, refer to the Safety Chapter of the
Ultrasound system User’s Manual.
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.
GE Medical Systems (China) Co., Ltd. +86 510 85225888 +86 510 85226688
No.19 Changjiang Road
Wuxi National Hi-Tech Dev. Zone
214028 Jiangsu China
TELEPHONE / FAX
AUTHORIZED REPRESENTATIVE NUMBER
The ___location of the CE marking is shown in the Safety chapter of the User
manual.
Authorized EU Representative:
GE Medical Systems SCS
283 rue de la Minière 78530 BUC, France
Site Preparations
2-1 Overview
CAUTION If the Ultrasound system is very cold or hot, do not turn on its
power until it has had a chance to acclimate to its operating
environment.
Degree F 23.9 28.4 32.9 37.4 104 108.5 113 117.5 122 131 140
hours 3 2 1 0 0 1 2 3 4 6 8
CAUTION Ensure that the probe face temperature does not exceed the
normal operation temperature range.
CAUTION The Vivid T8/Vivid T8 Pro system and probe connector is not
waterproof. Do not expose the device to water or any kind of
liquid.
2-2-2-3 Cooling
2-2-2-4 Lighting
CAUTION Power outage may occur. The Vivid T8/Vivid T8 Pro requires a
dedicated single branch circuit. To avoid circuit overload and
possible loss of critical care equipment, make sure you do not
have any other equipment operating on the same circuit.
IEC 61000-4-11 < 5%T (> 95% dip) for < 5%T (> 95% dip) for Mains power
0.5 cycle; 0.5 cycle; quality should be
Voltage dips, short
interruptions and 40%T (60% dip) for 5 40%T (60% dip) for 5 that of a typical
voltage variations cycles; cycles; commercial or
on mains supply hospital
70%T (30 dip) for 25 70%T (30 dip) for 25
cycles; cycles;
environment.
< 5%T (>95% dip) for 5 < 5%T (>95% dip) for 5
sec sec
Be aware of Radio • Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI
Frequency sources sources.
• Special shielding may be required to eliminate interference problems caused by
high frequency, high powered radio or video broadcast signals.
Ground the Poor grounding is the most likely reason an Ultrasound system will have noisy
Ultrasound system images. Check grounding of the power cord and power outlet.
Replace all screws, • After you finish repairing or updating the Ultrasound system, replace all covers
Radio Frequency and tighten all screws.
gaskets, covers, • Any cable with an external connection requires a magnet wrap at each end.
cores • Install all covers. Loose or missing covers or Radio Frequency gaskets allow
radio frequencies to interfere with the ultrasound signals.
Replace broken If more than 20% or a pair of the fingers on an Radio Frequency gasket are
Radio Frequency broken, replace the gasket. Do not turn on the Ultrasound system until any loose
gaskets metallic part is removed.
Do not place labels Where applicable, never place a label where Radio Frequency gaskets meet the
where Radio Ultrasound system. Otherwise, the gap created will permit Radio Frequency
Frequency gaskets leakage. Or, if a label has been found in such a position, move the label.
touch metal
Use GE specified The interconnect cables are grounded and require ferrite beads and other
harnesses and shielding. Also, cable length, material, and routing are all important; do not change
peripherals from what is specified.
Take care with Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
cellular phones
Properly route Where applicable, do not allow cables to lie across the top of the Card Rack or
peripheral cables hang out of the peripheral bays. Loop the excess length for peripheral cables
inside the peripheral bays. Attach the monitor cables to the frame.
CAUTION Ensure that the probe face temperature does not exceed the
normal operation temperature range.
CAUTION Check the room temperature before you use the probe.
CAUTION Ensure that the probe face temperature does not exceed the
normal operation temperature range.
11
10
9
8 12
13
7
6 14
1
1. Door – at least 762 mm (30 6. Examination Table – 1930 x 12. Network Interface
inches) 610 mm (76 x 24 inches) 13. 457 mm (18 inches) distance
2. Film Viewer 7. Footswitch of Ultrasound system from
3. Counter Top, Sink with hot 8. Stool wall or objects
and cold water and Supplies 9. Ultrasound system 14. GE Cabinet for Software and
Storage 10. External Peripherals Manuals
4. Linen Supply 11. Dedicated Power Outlet -
5. Probes/Supplies Circuit Breaker protected and
easily accessible
10 11 15
12
13 14 16
2 3 4 5
7
1
17
18
Figure 2-3. Suggested Room with EchoPAC PC workstation and Ultrasound Scanner
None.
Supported networks:
10/100 Mbps Ethernet/DICOM network (option)
Commercial devices such as laser cameras, printers, VCRs and external monitors,
usually exceed allowable leakage current limits and, when plugged into separate AC
outlets, are in violation of patient safety standards. Suitable electrical isolation of such
external AC outlets, or providing the device with extra protective earth, will be required
in order to meet UL60601-1 and IEC60601-1 / IEC60601-1-1 standards for electrical
leakage.
2.12.20DV (UL60601-1:2003)
In area in which patients are normally cared for, the patient vicinity is the space with
surfaces likely to be contacted by the patient or attendant who can touch the patient.
This encloses a space within the room 1.83 m (6 ft.) beyond the perimeter of the bed
(examination table, dental chair, treatment booth, and the like) in its intended ___location,
and extending vertically 2.29 m (7.5 ft.) above the floor.
1. Patient environment
Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI
ES60601-1:2005)
Such an area is an environment in which medical diagnosis, monitoring or treatment is
carried out. It is very difficult to attach unique dimensions to the PATIENT
ENVIROMENT.
In practice a distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel
stand and a horizontal distance of 1,5 m (4.9 ft.) have justified themselves as
indicative of the dimensions of the Patient Environment.
The patient environment/vicinity will be depicted as a dashed line in this procedure.
See example below.
1. Patient environment
System Setup
3-1 Overview
CAUTION DO NOT wear the ESD wrist strap when you work on live
circuits and more than 30 V peak is present.
CAUTION DO NOT operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling
require this.
CAUTION If the Ultrasound system is very cold or hot, do not turn on its power
until it has had a chance to acclimate to its operating environment.
Degree F 23.9 28.4 32.9 37.4 104 108.5 113 117.5 122 131 140
hours 3 2 1 0 0 1 2 3 4 6 8
3-3-4-1 Overview
Description Illustration
Tilt Watch
3-3-5-1 Overview
1. Is damage apparent?
• If YES; continue with the instructions in
3-3-5-5 ‘Damage in transportation’ on
page 3-11.
• If NO; continue with the next step.
1 - Red Color
1. Tilt Indicator
NOTE: Before cutting the straps, check Tilt Tag to make sure it has not
been triggered. If damaged, report it to the carrier. If not, then
cut the straps around the crate.
Step Task
CAUTION Please carefully unpack the system, and do not dispose the
package of Vivid T8/Vivid T8 Pro, so that it can be reused for
service.
NOTE: Please check the Vivid T8/Vivid T8 Pro console is well assembly
after unpacking the system.
11. With one hand holding the control panel and the
other hand holding the rear handle, move the
whole system down to the ground.
12. Remove all the covers and foams from the unit.
Verify that the mains voltage specified for the Vivid T8/Vivid T8
Pro is available on-site.
Refer to the latest revision of the User Manual for a full list of
product labels prior to serving the system.
Part Power
Number Description Voltage Tolerances consumntion Frequency
NOTE: USB Flash Drive approved for Vivid T8/Vivid T8 Pro are verified
for EMC performance according to EN55011 class B. The use of
any other USB Flash Drive will compromise this verification, and
may cause interference on Vivid T8/Vivid T8 Pro itself, or on
other electronic devices.
For approved models, please refer to Chapter 9.
Insert the USB Flash Drive in one of the USB ports on the Vivid
T8/Vivid T8 Pro.
Connect the cable to the S-Video Out port and the external
monitor. Select S-Video in the list of signal source menu on the
external monitor.
NOTE: S-Video and composit out port are not supported on Vivid T8
system which is originally installed with software R2.x.x.
3-8-1 Overview
This section describes how to install and configure the
peripherals validated for the Vivid T8/Vivid T8 Pro.
About the operation check-out of peripherals, 4-3-33 ‘Peripheral
checks’ on page 4-41
Weight
Description (kg) Power Control Model
2 Paper Roll 1
3 USB cable 1
2 Paper Roll 1
4 USB cable 1
• Digital Printer
2 Paper Roll 1
3 USB cable 1
2 Paper Roll 1
3 USB cable 1
2 USB Cable 1
• 3 Pedal Footswitch
3-8-3-1-1 Tools
No special tools needed.
3-8-3-1-2 Manpower
One person 5 min.
3-8-3-1-3 Preparations
1. Unpack B/W Printer.
8. Select Configure.
3-8-3-2-1 Tools
No special tools needed.
3-8-3-2-2 Manpower
One person 5 min.
3-8-3-2-3 Preparations
1. Unpack the Sony UP-D25MD Printer.
8. Select Configure.
3-8-3-3-1 Tools
No special tools needed.
3-8-3-3-2 Manpower
One person 5 min.
3-8-3-3-3 Preparations
1. Unpack the HP Officejet 100 Printer.
3-8-3-4-1 Tools
No special tools needed.
3-8-3-4-2 Manpower
One person 5 min.
3-8-3-4-3 Preparations
1. Unpack the UP-D897/UP-D898 MD Printer.
3-8-3-5-1 Tools
No special tools needed.
3-8-3-5-2 Manpower
One person 5 min.
3-8-3-5-3 Preparations
1. Unpack the Footswitch.
2. Ensure no physical damage.
3-8-3-6-1 Tools
No special tools needed.
3-8-3-6-2 Manpower
One person 5 min.
3-8-3-6-3 Preparations
1. Unpack the USB2.0 HDD.
2. Ensure no physical damage.
3-8-3-7-1 Tools
No special tools needed.
3-8-3-7-2 Manpower
One person 5 min.
3-8-3-7-3 Preparations
1. Unpack the ECG.
2. Ensure no physical damage.
• Allow SR
If SR is enabled, all M&A that is supported by DICOM is
sent to the DICOM server (in a separate job).
• Allow SR Private Data
By default, this function is disabled. It is intended for
receivers that can handle “Private Data”, such as
CA-1000.
• Signed Doppler Velocities
It is disabled by default. It means that signs for Doppler
Velocities are removed in the DICOM SR.
• MPPS
If enable MPPS, check the check-box and select MPPS.
In the dialog, enter IP address, Name, AE Title and port
Number.
3-9-5 DICOM SR
DICOM Structured Reporting (SR) is a standardized for medical
results. Vivid T8/Vivid T8 Pro supports the specialized form for
Adult Echo Ultrasound (TID 5200 Echocardiography Procedure
Report) and Vascular Ultrasound (TID 5100 Vascular Ultrasound
Procedure Report) for M&A results.
With the DICOM SR support, M&A for an exam can be sent at
the end of the exam or when exported from local archive. The
destination can be either a server on the network or a removable
media (DICOM Media), depending on the DICOM dataflow
selected.
TID5200 Echocardiography Procedure Report is sent if the
exam contains M&A from category Cardiac/Pediatric (heart) and
Vascular/Abdominal categories, two SR documents are sent.
TID5200 Echocardiography Procedure Report and TID 5100
Vascular Ultrasound Procedure Report do not support all M&A
results from Vivid T8/Vivid T8 Pro. They are limited to the
following:
• No unassigned measurement.
• Not modifies Simpson or Bullet methods.
• Basic derivations (Average, last, Min and Max), no
references between the derived measurements and the
ones they were made from.
• Wall Motion Scoring: individual segment scores only
according to 16-segment model, no graded hypokinesis
(only Hypokinesis is used).
DICOM SR must be activated for each DICOM device.
1. Press F2 on the control panel and log on as admin.
2. Select Connectivity-> Dataflow, the dataflow sheet is
displayed.
3. Select the DICOM dataflow to configure in the Name
pull-down menu.
3-9-7-1 Overview
Remote
Database+ Database+
Remote DICOM DICOM DICOM
No Output Database Database Storage Storage Storage
Database X X
Remote X X
Database
DICOM X
Worklist
DICOM CD X
Read
DICOM USB X
device Read
Query/ X
Retrieve
Worklist/ X X
database
Worklist/ X X
remote
database
No input X
device
Figure 3-55.
NOTE: During and after setup, the documentation (i.e. CDs with
documentation, User Manuals, Installation Manuals, etc.) for the
Vivid T8/Vivid T8 Pro and the peripherals must be kept as part of
the original Ultrasound system documentation. This ensures that
all relevant safety and user information is available during the
operation and service of the complete Ultrasound system.
4-1 Overview
4-2-1 Overview
Some procedures are used more often than other. The intention
with this section is to keep the most used procedures in one
place.
WARNING Energy Control and Power Lockout for Vivid T8/Vivid T8 Pro.
When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.
4-2-2-1 Warnings
CAUTION Use only power supply cords, cables and plugs provided by or
designated by GE.
NOTE: Do not cycle the Circuit Breaker ON-OFF-ON in less than five
(5) seconds. When turning OFF the Circuit Breaker, the
Ultrasound system should de-energize completely before
turning the circuit breaker ON.
• Logoff
Use this button to log off the current user.
The system remains ON and ready for a new user to log on.
If the Logoff button is dimmed, it indicates that no user is
logged on to the unit at the moment.
• Shutdown
Use this button to shut down the system. The entire system
will shut down. It is recommended to perform a full shutdown
at least once a week.
If the Shutdown button is dimmed, use the key-combination
<Ctrl+Alt+Delete> to shut down the unit.
NOTE: To enable the key-combination <Ctrl+Alt+Delete>, the
dongle should be connected to the system.
• Cancel
Use this button to exit from the System-Exit menu and
return to the previous operation.
CAUTION DO NOT unplug and/or transport the unit until after the power
off sequence has been completed. Failure to do so may result
in corrupted patient files.
4-2-13 Backup
For more information, refer to the latest revision of the Vivid T8/
Vivid T8 Pro User Manual.
4-2-16 Where are the User Manuals and the Service Manual?
Online versions of the User Manuals are available via the help
function.
Both the User Manuals and the Service Manual are delivered as
PDF files on a CD-ROM. Paper copies may be ordered from
GE.
4-2-17 How to display or print the PDF files from the Manual CD?
1. Insert the CD-R disk (CD-ROM) into the CD-drive on a PC
or Laptop with Adobe Acrobat Reader.
CAUTION Do not try to use the Vivid T8/Vivid T8 Pro to read these files, it
will not work!
4-2-18-1 Manpower
4-2-18-2 Tools
4-2-18-3 Preparations
To get access to the trackball for cleaning, you must perform the
following steps:
1. Power down the system.
2. Disconnect the mains power cable from the wall outlet.
Follow these links if you need more information: 4-2-3 ‘Power
off’ on page 4-8
3. Separate the trackball and the gasket. Wipe off any oil or
dust from the trackball, gasket and the trackball housing
using a cleaner or cotton swab.
4. Assemble the trackball and gasket, then put it into the
housing and rotate it clockwise until its notches are set in
the position.
CAUTION When cleaning, make sure not to spill or spray any liquid into
the trackball housing (keyboard or system).
Power up the system and test that the trackball now works as
intended.
4-3-1 Overview
In this section, the functional checks for Vivid T8/Vivid T8 Pro
are described. Functional checks are used to verify that the
product works as intended. Functional checks may also be used
during troubleshooting.
4-3-3 Preparation
Turn on power to Vivid T8/Vivid T8 Pro. For detailed description,
4-2-2 ‘Power ON/Boot Up’ on page 4-5
4-3-8-1 Introduction
4-3-10 Preparations
• Connect one of the probes.
• Turn ON the scanner.
The 2D Mode is displayed (default mode).
4-3-15 Preparations
• Connect one of the probes to the scanner’s left-most probe
connector.
• Turn ON the scanner.
The 2D Mode window is displayed (default mode).
• Press MM on the Operator panel to bring up an M-Mode
picture on the screen.
Use the trackball to position the cursor over the required
area of the image.
4-3-17-1 Introduction
4-3-17-2 Preparations
• Adjust the Active mode gain to set the gain in the color flow
area.
Adjust Scale to the highest setting that provides adequate
flow detection.
NOTE: The scale value may affect FPS, Low Velocity Reject, and
Sample Volume.
Adjust Low Velocity Reject to remove low velocity blood
flow and tissue movement that reduces image quality.
Adjust Variance to detect flow disturbances.
Adjust Sample volume (SV) to a low setting for better flow
resolution, or a higher setting to more easily locate disturbed
flows
Adjust Frequency to optimize the color flow display. Higher
settings improve resolution. Lower settings improve depth
penetration and sensitivity. This does not affect the
frequency used for 2D and M-Mode.
NOTE: NOTE: Frequency setting may affect FPS, SV and Low
Velocity Reject.
Adjust Power to obtain an acceptable image using the
lowest setting possible.
NOTE: The Power setting affects all other operating modes.
Adjust the following settings to further optimize display of the
image:
• Use Invert to reverse the color assignments in the color flow
area of the display.
Use Tissue priority to emphasize either the color flow
overlay, or the underlying grey scale tissue detail.
Use Baseline to emphasize flow either toward or away from
the probe.
Use Radial and Lateral Averaging to reduce noise in the
color flow area. Radial and Lateral Averaging smooths the
image by averaging collected data along the same
horizontal line. An increase of the lateral averaging will
reduce noise, but this will also reduce the lateral resolution.
4-3-21-1 Introduction
4-3-21-2 Preparations
4-3-23-1 Introduction
4-3-23-2 Preparations
CAUTION DO NOT allow the probe head to hang free. Impact to the
probe head could result in irreparable damage.
1 Select the appropriate connected probe from the The probe activates in the currently-selected
probe indicators on the Touch Panel. operating mode. The probe’s default settings
for the mode and selected exam are used
automatically.
4 Test the probe in each active connector slot. It will display pictorial data each time.
Not all the types of RS probe connector can match the Vivid T8/
Vivid T8 Pro system.
1. Not match
2. Match
3. Match
4. Match
4-3-27-1 Introduction
4-3-27-3 Preparations
None
1 Connect the ECG harness to the connector The unit displays a straight curve along the
under the control panel. bottom edge of the image sector on the screen.
2 Connect the three leads to an ECG simulator, When connecting, the signal on the screen will
or be noisy.
Fasten the three ECG Pads to your body and When the connection is completed, a typical
connect the three leads to respective ECG clean ECG signal is displayed.
Pad.
4-3-28-1 Introduction
4-3-29 Preparation
• Connect one of the probes to the scanner.
• See 4-3-26 ‘Probe/Connectors Check’ on page 4-37 for info
about connecting the probes
For available probes, see 9-3-12 ‘Probe’ on page 9-36:
• Turn ON the scanner. The 2D Mode is displayed (default
mode).
Wheel Characteristics
5 Verify all of the customer’s options are set up Demo Option strings turn on
correctly.
5-1 Overview
5-2-3-2 Introduction
5-2-4-1 Description
Electrical Interface • High voltage input: +/-SHV (about +/-85V), +/-THV (about +/-70V)
• Low voltage input: +5v, -5v, +12V, +3.5V, +1.8V
• Probe and relay control signals
• Power on/off control signals
• I2C bus signals to control high voltage
• CWD signals
• DDI signals for display from CPU
• Audio signals from CPU
• USB signals from CPU
• Ethernet signals from CPU
5-2-5-1 Dscription
5-2-6-1 Description
5-2-7-1 Description
5-2-8-1 Description
5-2-9-1 Description
5-3-1 Overview
The AC Power assy’s main tasks are to isolate and output to the
DC/DC unit which is inside the system console. The input of AC
power pack will be the AC outlet and it’s universal, the range is
AC 90V-264V, 47-63Hz. And no main power switch located on
this power pack.
5-3-2 AC Power
The mains cord has plugs in one side end. A male plug connects
to the mains outlet on site.
The mains voltage is routed to the AC power pack through a
Circuit Breaker located on the site.
The Circuit Breaker is of the auto fuse type, if for some reason
the current grows to high, the switch will automatically break the
power.
From the Main Circuit Breaker, the AC power is routed via an
Inrush Current Limiter to a internal outlet connector for the
Mains Transformer.
5-4-1 Introduction
The Service Platform contains a set of software modules that
are common to all PC backend ultrasound and cardiology
systems. The Common Service Platform will increase service
productivity and reduce training and service costs.
5-4-2-1 Internationalization
Click the InSite ExC icon at the bottom of the display screen.
Select Service Desktop in the pop-up screen. It links the user
or the Field Engineer (FE) to the service login screen.
5-4-2-3 Access/Security
NOTE: Online Center access to the scanner requires the password and
they must have “Disruptive” permission and custormer input to
run diagnostics.
5-4-2-3 Access/Security(continued)
NOTE: Follow these steps if you want to exit to the Windows Desktop
when the system is active. The Service Dongle must be plugged
in to one of the USB ports.
1. Insert the Service Dongle into a USB port.
2. Go back to the scanning screen and press Ctrl+Alt+R.
3. Select Yes to continue.
Figure 5-19.
1 Warning Green
2 Warning Blue
3 Error Red
5-4-5-1 Logs
5-4-5-1 Logs(continued)
• TxPower
Log entry headings include Time Stamp; CPS NSU; CPS
SHVN; CPS HUM0.
• Temperature
Log entry headings include Time Stamp; MST FanSpeed_1;
MST FanSpeed_2; BEP CPU_TEMPERATURE; BEP
CHIPSET_TEMPERATURE; BEP SYS_TEMPERATURE;
MST MVP_TEMPERATURE; MST AFE_TEMPERATURE;
CPS DSV_TEMPERATURE.
• Dicom
Log entry headings include Time Stamp; Error Level;
Package; Message.
• Download
Log entry headings include Time Stamp; Error Level;
Package; Message.
• Network
Log entry headings include Error Level; Package; Message.
5-4-5-2 Utilities
The two sub-menus of the Utilities category are Plot Log and
Plot Page.
• Plot Log
Allows for the color coded plot of all Log contents with the
package on the “x” axis and incident count on the “y” axis.
NOTE: The screen can not display all the log contents. Move up the
screen to display the all the log contents.
• Plot Page
Allows for the color coded plot of all Log contents with the
package on the “x” axis and incident count on the “y” axis.
5-4-5-3 Search
5-4-5-4 Exit
The sub-menu, Exit Log Viewer, returns the user to the Service
Home Page.
5-4-6 Diagnostics
Detailed Diagnostic information, 7-5 ‘Global Service User
Interface (GSUI)’ on page 7-16
5-4-8 Calibration
The Calibration page is intended to contain the tools used to
calibrate the system.
5-4-9 Configuration
The Configuration page is intended to be used to setup various
configuration files on the system.
The Service Platform is the access and authorization control for
remote access to the configuration subsystem.
The enable/disable of software options can be done from this
Configuration page.
5-4-10 Utilities
The Utilities page contains several miscellaneous tools.
5-4-11 Replacement
The Replacement page is intended to contain the tools used to
track replacement parts used in the system.
5-4-12 PM
The PM page is intended to contain the tools used in periodic
maintenance of the system.
Service Adjustments
6-1 Overview
Diagnostics/Troubleshooting
7-1 Overview
7-2-1 Overview
There may be a time when it would be advantageous to capture
trouble images and system data (logs) for acquisition to be sent
back to the manufacturer for analysis. There are different
options to acquire this data that would give different results
7-5-2-1 Button
This is an editable text field that will only accept numeric values
with 4 digits or less. When the button is configured as an
“execute” button and pressed, the loop count field will be
queried to determine the number of times to execute the
diagnostic.
7-5-3-1 Utilities
NOTE: For R2.x.x, you need to repeat all the steps above after you
restart the system if you want to activate virtual dongle.
7-5-3-3-1 GFS
• GFS Swept Demodulator Test performs a signal path test of
the swept demodulator FPGA on the GFS.
• GFS Front-End Interface Test tests that the GFS can access
Front-End boards.
• GFS Analog Test.
• GFS Memory Access Test tests that GFS can access to the
internal, external, external cache memory spaces.
• Front End Interface FPGA Test reads the version of the GFE
FPGA.
• GFS Fixed Demo Test: GFS Fixed Demodulator signal path
test.
• DSP Master Clock Test tests DSP Master Clock.
• GFS Swept Demodulator Long Test.
7-5-3-3-2 System
• CPU Temperature Test.
• CPS Temperature Test.
• WMST Temperature Test.
• WMST Voltage Test.
• CPS Voltage Test.
• FPGA Version Test.
• HV_STOP Test tests HV-STOP mechanism and checks
each board is able to assert HV_STOP using its HV_STOP
source.
7-5-3-3-3 Memory
• Callisto Memory Test.
NOTE: The Callisto Memory test may fail if it is performed with other
tests at the same time.
7-5-3-3-4 AnalogReceive
• Noise Floor Test.
7-5-3-3-5 AnalogCW
• aCW IQ Symmetry Test
7-5-3-3-9 PC
• Essential Test tests: PCI, PCI Express, CPU, Memory, HD
Disk and Video.
• Hard Drive Long tests functionality of the hard drive.
• Hard Drive Short tests functionality of the hard drive.
• Memory tests the memory on the mother board.
• Network Adapter: Network calbe must be connected.
• System board tests the real time clock.
• Video tests functionality of video adapters.
7-5-3-3-10 PC Interactive
• AVI playback tests playing back an AVI file.
• Click “Play” to run the test. If the test is successful, you
will see a brief video clipo with audio. For more
information about the test, click “More Information”.
• Click “Pass” if the test successfully reproduces the
video clip.
• Click “Fail” if the test is unable to successfully reproduce
the video clip.
• Click “Cancel” button to quit the test without recording a
test result.
• Keyboard
• Press each key on the keyboard and it will be added to
the History. Hold down a key to test the repeat of that
key. To cancel, click Cancel or press Alt-X.
• Special purpose keys like volume control or Internet
access keys may not be detected. To test the Fn key of
a notebook computer, hold down the Fn key while
pressing another key.
• Note: This diagnostic is intended to verify keyboard
keys are in good working order. It is not intended to
veriy that keyboards produce desired characters.
• Trackball
• The Mouse Status Test verifies the cursor position and
mouse button state. When a mouse button is pressed,
the corresponding button on the picture will change
color. If the mouse is a wheel or scroll mouse, an arrow
will indcate the direction the wheel is being rotated.
Clicking the wheel will flash the picture of the mouse in
the Mouse Status Test area.
• The Drag and Drop Test verifies a mouse can
successfully perform drag and drop operations. Left
click the picture of the CD and drag is onto the picture of
the drive. If successful, the picture will change.
• The Double Click Test verifies a mouse can successfully
perform double-click operations. Double-click on the
picture of the monitor. If successful, the picture will
change.
• Sound Test generates sounds for testing the speakers.
• USB Ports Test lists USB Devices.
CAUTION DO NOT allow the probe head to hang free. Impact to the
probe head could result in irreparable damage.
7-5-3-5 Transmit
• GeckoScope
7-7 Troubleshooting
7-7-1 Console Troubleshooting Trees
7-7-1-1 System Doesn’t Boot
Colored streaks appear in Check for presence of magnetic sources near the monitor.
image Eliminate the sources and then degauss the monitor.
Only replace with a new MST System still can recognize the System still can recognize the
board. Keep using the existing serial numbers stored in the HDD. software option keys stored in
HDD without any software reload User no need take any action. the HDD. User no need take
or re-install. any action.
Replace with a new MST board. No serial number in MST or HDD. All existing software option keys
Replace with a new HDD, or use System will ask for serial number are lost. User need re-enter the
existing HDD but have software when first power on. User need software option keys.
reload or re-install to full disk. enter the correct serial numbers.
Replace with a new MST board. System still can recognize the System still can recognize the
Use existing HDD but have serial numbers stored in the HDD. software option keys stored in
software reload or re-install to C User no need take any action. the HDD. User no need take
disk only. any action.
Replace with a new CPU System still can recognize the System still can recognize the
module. serial numbers stored in the HDD. software option keys stored in
User no need take any action. the HDD. Please remember to
set the correct system time.
Some DEMO keys will expire if
date is incorrect.
Replace with another MST board The system serial number stored The software options keys
(with SN inside). Keep using the in MST board is different with the stored in HDD will be invalid
existing HDD. No software reload one in HDD. User need enter the since system serial number
or re-install. correct serial numbers. change. User need enter the
new software option keys which
match with the serial number in
the MST board.
NOTE: The serial number can be found on the rating plate on the
rear side of the system.
NOTE: Make sure the system is shut down after the serial number
is reset.
3. Power on the system, input the option keys if the dialog
displays.
WARNING If you rewrite the serial number after the system exits to
Windows with service dongle or the data is failed to save on
Local Archive, please follow the steps below:
1. Delete serialno.txt in D Disk.
2. Disconnect the service dongle and then reboot the system.
3. Follow the steps on page 7-50 to rewrite the Serial number
again.
5. Change the value to “-1”, and then click [Write All] button.
7. Input the correct SN. The system will restart, and then input
the option key.
Replacement Procedures
8-1 Overview
8-2-1 Warnings
WARNING Energy Control and Power Lockout for Vivid T8/Vivid T8 Pro.
When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.
8-2-1 Warnings(continued)
NOTE: Use an ESD compatible work space or the ESD-kit during parts
replacement.
8-3 Disassembly/Re-assembly
CAUTION Do not wear the ESD wrist strap when you work on live circuits
and more than 30V peak is present.
Part
No Name Part No. QTY Screw Description Screwdriver Description
R1 Touch Panel
Paper Tray
Rear Panel
Cable Tray
Speaker 8-26
Trackball 8-41
AN Keyboard 8-46
Castor 8-150
Base 8-153
When you adjust LCD position, pay attention to the pinch point
between the LCD and touch panel in case of any hurt of your
hand.
8-4-1-2 Tools
8-4-1-3 Preparation
Speaker 8-26
Trackball 8-41
AN Keyboard 8-46
8-5-1-1 Tools
8-5-1-2 Preparation
8-5-2 Speaker
Purpose: This is a description on how to remove and replace the
Speaker.(5487238-S)
8-5-2-1 Tools
8-5-2-2 Preparation
8-5-2 Speaker(continued)
8-5-3-1 Tools
8-5-3-2 Preparation
8-5-4-1 Tools
8-5-4-2 Preparation
3. Unscrew 3 screws.
8-5-5-1 Tools
8-5-5-2 Preparation
8-5-6-1 Tools
8-5-6-2 Preparation
8-5-7 Trackball
Purpose: This is a description on how to remove and replace the
Trackball.(5447726-S)
8-5-7-1 Tools
8-5-7-2 Preparation
8-5-7 Trackball(continued)
8-5-8-1 Tools
8-5-8-2 Preparation
Table 8-17: Removal Procedure for Power and Freeze button Kit
Table 8-17: Removal Procedure for Power and Freeze button Kit
8-5-9 AN Keyboard
Purpose: This is a description on how to remove and replace the
AN Keyboard.(5498252-2-S)
8-5-9-1 Tools
8-5-9-2 Preparation
8-5-10-1 Tools
8-5-10-2 Preparation
2. Disconnect 3 connectors.
8-5-11-1 Tools
8-5-11-2 Preparation
8-5-12-1 Tools
8-5-12-2 Preparation
9. Unscrew 3 screws.
8-5-13-1 Tools
8-5-13-2 Preparation
8-5-14-1 Tools
8-5-14-2 Preparation
8-5-15-1 Tools
8-5-15-2 Preparation
4. Unscrew 1 screw.
NOTE: Fix the black sheet on the flexible arm assy and then install the
flexible arm assy on the UI adapter with lock plate.
NOTE: To adjust the arm flexible or stable, loosen or fasten the screw
shown as below.
8-5-16-1 Tools
8-5-16-2 Preparation
8-6-3-1 Tools
8-6-3-2 Preparation
8-6-4-1 Tools
8-6-4-2 Preparation
8-6-5-1 Tools
8-6-5-2 Preparation
8-6-6-1 Tools
8-6-6-2 Preparation
8-6-7-1 Tools
8-6-7-2 Preparation
8-6-8-1 Tools
8-6-8-2 Preparation
8-6-9-1 Tools
8-6-9-2 Preparation
5. Unscrew 2 screws.
After the internal box assy is replaced, the serial number on the
Harddisk will not match that on the VPD. When powering the
system, the system will indicate to rewrite the serial number,
refer to 7-7-4 ‘Rewrite the Serial Number’ on page 7-50.
8-6-10-1 Tools
8-6-10-2 Preparation
Table 8-34: Removal Procedure for Harddisk Assy (5487561-S for R1.x.x, 5694056-S
for R2.x.x)
3. Unscrew 2 screws.
Table 8-34: Removal Procedure for Harddisk Assy (5487561-S for R1.x.x, 5694056-S
for R2.x.x)
Table 8-35: Removal Procedure for Harddisk Assy (5755632-S for R2.0.3 and above))
2. Unscrew 2 screws.
8-6-11-1 Tools
8-6-11-2 Preparation
Table 8-37: Removal Procedure for Internal Battery (For R2.0.3 and above)
Table 8-37: Removal Procedure for Internal Battery (For R2.0.3 and above)
8-6-12-1 Tools
8-6-12-2 Preparation
8-6-13-1 Tools
8-6-13-2 Preparation
Table 8-39: Removal Procedure for I/O Board PWA (5456663-S for R1.x.x and
5456663-4-S for R2.x.x)
Table 8-39: Removal Procedure for I/O Board PWA (5456663-S for R1.x.x and
5456663-4-S for R2.x.x)
4. Unscrew 6 screws.
3. Unscrew 6 screws.
8-6-14-1 Tools
8-6-14-2 Preparation
4. Disconnect 1 connector
and untie 2 cable hooks.
6. Unscrew 2 screws.
8-6-15-1 Tools
8-6-15-2 Preparation
Table 8-42: Removal Procedure for WPWR PWA (5473829-S for R1.x.x, 5537639-2-S
for R2.0.0)
2. Unscrew 1 screw.
Table 8-42: Removal Procedure for WPWR PWA (5473829-S for R1.x.x, 5537639-2-S
for R2.0.0)
Table 8-42: Removal Procedure for WPWR PWA (5473829-S for R1.x.x, 5537639-2-S
for R2.0.0)
Table 8-43: Removal Procedure for WPWR PWA (5537638-3-S for R2.0.3 and above)
8-6-16-1 Tools
8-6-16-2 Preparation
8-6-17-1 Tools
8-6-17-2 Preparation
After the CPU is replaced, the serial number on the Harddisk will
not match that on the VPD. When powering the system, the
system will indicate to rewrite the serial number, refer to
7-7-4 ‘Rewrite the Serial Number’ on page 7-50.
NOTE: Please make sure the system BIOS time has been updated to
the current time when rebooting the system after the CPU
replacement.
1. Press Power button on the Control Panel to power on the
system, press Config. on the control panel immediately.
3. In the BIOS Main page, update the BIOS time to the current
time.
12. Press Spooler on the cotrol panel and then select Yes to
save and exit BIOS.
8-6-18-1 Tools
8-6-18-2 Preparation
8-6-19-1 Tools
8-6-19-2 Preparation
8-6-20-1 Tools
8-6-20-2 Preparation
8-6-21-1 Tools
8-6-21-2 Preparation
8-6-22-1 Tools
8-6-22-2 Preparation
Table 8-52: Removal Procedure for Battery and SATA Connection PWA
8-6-23-1 Tools
8-6-23-2 Preparation
8-6-24-1 Tools
8-6-24-2 Preparation
Table 8-54: Removal Procedure for battery bracket (5755630-S for R2.0.3 and above)
Castor 8-150
Base 8-153
8-7-1-1 Tools
8-7-1-2 Preparation
8-7-1-6 Castor
8-7-1-7 Tools
8-7-1-8 Preparation
8-7-1-12 Base
8-7-1-13 Tools
8-7-1-14 Preparation
6. Unscrew 4 screws.
8-8-1-2 Tools
8-8-1-3 Preparation
8-8-1-9 Tools
8-8-1-10 Preparation
8-8-1-16 Tools
8-8-1-17 Preparation
Table 8-62: Removal Procedure for one box to KBD cabke kit
1. Unscrew 8 screws.
Table 8-62: Removal Procedure for one box to KBD cabke kit
Table 8-62: Removal Procedure for one box to KBD cabke kit
Table 8-62: Removal Procedure for one box to KBD cabke kit
8-8-1-22 Tools
8-8-1-23 Preparation
• No need
Table 8-63: Removal Procedure for cable clip SVC kit for power cable
CAUTION Ensure that the retaining clamp for the power plug is fixed
firmly.
8-9-1 Manpower
One person, 10 minutes,
8-9-2 Tools
• Antistatic brush and/or antistatic vacuum cleaner
8-9-3 Preparations
To get access to the trackball for cleaning, you must perform the
following steps:
1. Power down the system.
2. Disconnect the mains power cable from the wall outlet.
Follow these links if you need more information: 4-2-3 ‘Power
off’ on page 4-8
3. Separate the trackball and the gasket. Wipe off any oil or
dust from the trackball, gasket and the trackball housing
using a cleaner or cotton swab.
4. Assemble the trackball and gasket, then put it into the
housing and rotate it clockwise until its notches are set in
the position.
CAUTION When cleaning, make sure not to spill or spray any liquid into
the trackball housing (keyboard or system).
8-10-1 Manpower
One person, 5 minutes,
8-10-2 Tools
• None
8-10-3 Preparations
To get access to the air filter for cleaning, you must perform the
following steps:
1. Power down the system.
2. Disconnect the mains power cable from the wall outlet.
Follow these links if you need more information: 4-2-3 ‘Power
off’ on page 4-8
8-11-6-1 Overview
CAUTION If you select [a], ALL existing software and data will be erased.
If backup has not been performed, all data like Patient
Database, System Configuration and User Configurations
(Customer Presets) will be lost.
CAUTION If you select [a], ALL existing software and data will be erased.
If backup has not been performed, all data like Patient
Database, System Configuration and User Configurations
(Customer Presets) will be lost.
WARNING Selection of [d] DOES NOT meet the GE Global Secure Wipe
Standard. Back up the data before executing.
6. The system starts to upgrade. (for selection [a], [b], and [c])
NOTE: The download step can be paused. While paused, you can
return to normal operation. However, once the software
installation has begun, the system is not usable until the
software installation is done. While installing, DO NOT turn
off system power.
NOTE: A typical software update of about 600 Mb may take up to
45 minutes to download, but times may vary depending on
your ___location and network connection.
• Pause: Pauses the software download process. If you
select Pause, you can cancel out of this dialog and
return to normal scanning or you can power off the
scanner. A paused download can be resumed by
logging in as Administrator, pressing the power switch,
and selecting Resume.
• Resume: Press Resume to continue the software
download.
CAUTION Perform a check for all the features listed. You MUST
ensure that the entire system functions normally as
expected.
These verification results are tracked for regulatory
purposes, sent back to GE for tracking, and approved with
your signature.
Select DICOM You can modify, add or remove the selected DICOM.
8-13-1 Overview
This section provides the information for check after FRU
replacement.
• Perform required Functional and/or Leakage Current tests
based upon the FRU being replaced.
Equipment passed all required tests and is ready for use.
• Clarify the scripts to debrief a Service Dispatch using your
pole's dispatch tool. Use this script in the Service
Comments when debriefing a Service Dispatch.
Leakage Current meets allowable limits. Equipment passed
all required tests and is ready for use.
Basic Functional Check Arm Support Kit • 4-3-35 ‘Mechanical Functions Checks’ on
Checks Check Flexible Arm page 4-41
Check Internal Box Assy • 4-2-2 ‘Power ON/Boot Up’ on page 4-5
Check Internal Battery • 4-2-3 ‘Power off’ on page 4-8
Check ACDC Module • 4-3-26 ‘Probe/Connectors Check’ on page 4-37
Check I/O Board PWA • 4-2-4 ‘LCD Monitor position adjustment’ on
Check WPWR PWA page 4-10
Check Relay Assy • 4-3-8 ‘2D Mode (B mode) Checks’ on page 4-26
Check CWD PWA • 4-3-13 ‘M Mode Checks’ on page 4-28
Check One box cable kit • 4-3-17 ‘Color Mode Checks’ on page 4-29
• 4-3-21 ‘PW/CW Doppler Mode Checks’ on
page 4-33
• 4-3-23 ‘Tissue Velocity Imaging (TVI) Checks’ on
page 4-35
• 4-3-25 ‘Basic Measurements’ on page 4-36
• 4-3-28 ‘Cineloop Check’ on page 4-40
LCD Assy Check LCD Test Pattern • 4-3-35 ‘Mechanical Functions Checks’ on
page 4-41
• 4-2-2 ‘Power ON/Boot Up’ on page 4-5
• 4-2-3 ‘Power off’ on page 4-8
• 4-3-26 ‘Probe/Connectors Check’ on page 4-37
• 4-2-4 ‘LCD Monitor position adjustment’ on
page 4-10
• Check LCD Test Pattern in Utility-> Test Pattern
LCD Cable Check LCD cable kit • 4-3-35 ‘Mechanical Functions Checks’ on
page 4-41
• 4-2-2 ‘Power ON/Boot Up’ on page 4-5
• 4-2-3 ‘Power off’ on page 4-8
• 4-3-26 ‘Probe/Connectors Check’ on page 4-37
• 4-2-4 ‘LCD Monitor position adjustment’ on
page 4-10
KBD Top Assy Check KBD Top Assy • 4-3-35 ‘Mechanical Functions Checks’ on
Check KBD Top Cover page 4-41
• 4-2-2 ‘Power ON/Boot Up’ on page 4-5
• 4-2-3 ‘Power off’ on page 4-8
• 4-3-8 ‘2D Mode (B mode) Checks’ on page 4-26
• 4-3-13 ‘M Mode Checks’ on page 4-28
• 4-3-17 ‘Color Mode Checks’ on page 4-29
• 4-3-21 ‘PW/CW Doppler Mode Checks’ on
page 4-33
• 4-3-23 ‘Tissue Velocity Imaging (TVI) Checks’ on
page 4-35
• 4-3-25 ‘Basic Measurements’ on page 4-36
• 4-3-28 ‘Cineloop Check’ on page 4-40
• Press Patient key to check if system can go to
Patient screen.
• Press Print Key (Factory default settings) to see if
the system can store images
• Press Comments key to see if can input
comments via AN keys
Left/Right Fan Check Fan Assy with cable • 4-3-35 ‘Mechanical Functions Checks’ on
Assy page 4-41
• 4-2-2 ‘Power ON/Boot Up’ on page 4-5
• 4-2-3 ‘Power off’ on page 4-8
SCNT FPC Check SCNT FPC • 4-2-2 ‘Power ON/Boot Up’ on page 4-5
• 4-3-8 ‘2D Mode (B mode) Checks’ on page 4-26
• 4-3-13 ‘M Mode Checks’ on page 4-28
• 4-3-17 ‘Color Mode Checks’ on page 4-29
• 4-3-21 ‘PW/CW Doppler Mode Checks’ on
page 4-33
• 4-3-23 ‘Tissue Velocity Imaging (TVI) Checks’ on
page 4-35
• 4-3-25 ‘Basic Measurements’ on page 4-36
• 4-3-28 ‘Cineloop Check’ on page 4-40
Battery and Check Battery and SATA • 4-2-2 ‘Power ON/Boot Up’ on page 4-5
SATA Connection PWA • 4-2-3-2 ‘Battery Status’ on page 4-9
Connection
PWA
AP2M PWA Check AP2M PWA • 4-2-2 ‘Power ON/Boot Up’ on page 4-5
• 4-2-3 ‘Power off’ on page 4-8
CMOS Battery Check CMOS Battery Power on the system. Check that the current date
and time is later than the date and time of last
bootup.
Battery Bracket Check Battery Bracket • Try to move the battery bracket and the battery
bracket is securely fixed and is not loose.
• 4-2-3-2 ‘Battery Status’ on page 4-9
Renewal Parts
9-1 Overview
ABBREVIATION DESCRIPTION
3D THREE DIMENSIONAL
Assy ASSEMBLY
KBD Keyboard
HW Hardware
SW Software
ME Mechanical
Part
Item Number Part Name Quantity FRU
LCD Assy
Keyboard
Assy
Body Assy
Base Assy
6 Probe 9-36
7 Peripheral 9-38
9 Manuals 9-41
LCD Assy
R1/R2 Flexible
ARM
R1 Touch Panel
R1/R2 Probe
holder kit
R1 Internal ECG
cable
R1/R2 AN KBD
R1 ECG PWA
R1 ECG PWA
R2 Internal battery
R2 SFPC PWA
R1 IO Board PWA
R1 ACDC module
R1 CPU Assy
R1 WPWR PWA
Note:
5809956-S is
latest version
and much
stronger than
5790989-S,
please order
5809956-S for
service
activities.
607 5479055-S One box to KBD HW Note: The latest BOM does not R1.x.x/R2.x.x RP
cable kit for LOGIQ include 5448555 as part EOL.
F series Please contact Eng if needed.
9-3-12 Probe
Table 9-9: Probes for Vivid T8/Vivid T8 Pro
Center Image
Part Frequency
Item Part Name Number Illustration (MHz) Qty FRU
Center Image
Part Frequency
Item Part Name Number Illustration (MHz) Qty FRU
9-3-13 Peripheral
Table 9-10: ECG cable for Vivid T8/Vivid T8 Pro
800 AHA Solution 2269979 Cable: Main ECG Americas & Japan 1
804 IEC Solution 2269980 Cable: Main ECG Europe & ROW 1
814 ECG Cable 2106305-003-S ECG TRUNK CABLE, 3/5-LEAD, IEC, 3.6 M/12 FT. - 1
Kit - EU service edition
818 ECG Cable 2106305-001-S ECG TRUNK CABLE, 3/5-LEAD, AHA, 3.6 M/12 FT. - 1
Kit - US service edition
Footswitch
USB Stick
Printer
828 5133106-2 (H48542LY) SONY UPD25 Color Printer CHN kit (for R1 only) 1
829 5133107-2 (H48542LZ) SONY UPD25 Color Printer USA kit (for R1 only) 1
830 5133108-2 (H48552LA) SONY UPD25 Color Printer EUP kit (for R1 only) 1
831 5133109-2 (H48552LB) SONY UPD25 Color Printer JPN kit (for R1 only) 1
Biopsy Kit
9-3-14 Manuals
Table 9-12: Manuals for Vivid T8/Vivid T8 Pro
Replaced
Item Part Number Description by Qty FRU
Replaced
Item Part Number Description by Qty FRU
9-3-14 Manuals(continued)
Table 9-13: Manuals for Vivid T8/Vivid T8 Pro
10-1 Overview
10-2 Warnings
CAUTION Do not pull out or insert circuit boards while power is on.
CAUTION Do not operate this Ultrasound system unless all board covers
and frame panels are securely in place. System performance
and cooling require this.
Per
Facilities
Service at Indicated QA
Time Daily Weekly Monthly Program Notes
Clean Console •
Clean LCD •
Per
Facilities
Service at Indicated QA
Time Daily Weekly Monthly Program Notes
NOTE: For a list of required tools for servicing the Vivid T8/Vivid T8 Pro,
refer to chapter 8.
9-44579 Wrench Open End 1/2 - 9/16 9-XL9974MM Xcelite-hex Blade 2.5mm
9-44579 Wrench Open End 1/2 - 9/16 9-XL9975MM Xcelite-hex Blade 3mm
9-41581 Screwdriver, Blade 3/16 in. × 4 9-45341 Pliers Vice Grip 10 inch
in.
9-39451 20' Steel Tape, locking Spring 9-3001 Xacto Pen Knife
load
9-GH807 Ratchet, Offset, Slotted 9-HT62002 Solder Aid, Fork and Hook
9-41584 Screwdriver, slotted 1/4 in. × 6 9-GH300ME Steel Rule Metric 6 inch
in.
9-46677 Hex Keys, 20 pc., Metric 9-XL9924 Xcelite-hex Blade 1/8 inch
9-34701 1/4 in. Standard Socket set (19 9-XL9925 Xcelite-hex Blade 5/32 inch
pc)
9-43499 1/2 inch Socket 1/4 inch drive 9-XL9926 Xcelite-hex Blade 3/16 inch
9-65283 Case 8.5 in. × 4.5 in. × 2 in. 9-45072 Pliers 6 inch Diagonal
Deep
9-GH408 Tweezers
9-45381 Pliers, Arc Joint 9 1/2 inch 9-44067 Socket 1 1/16 in. for 1/2 in.
drive
9-45092 Pliers, Linesman 8 1/2 inch 9-42679 Socket 10MM Hex for 1/2 in.
drive (2273333)
9-42882 Punch, Pin 3/32 inch 9-44262 Extension 10 inch for 1/2 in.
drive (2273405)
9-42884 Punch, Pin 5/32 inch 9-4258 3/8 inch to 1/2 inch Adapter
9-42886 Punch, Pin 1/4 inch 9-34374 3/8 inch Metric Socket Set -
12 PT
9-31277 File, Half Round, Bastard 8 9-52068 Tap and Drill Set
inch
Anti Static Kit Kit includes anti–static mat, wrist strap and cables
for 200 to 240V system
3M #2204 Large adjustable wrist strap
3M #2214 Small adjustable wrist strap
3M #3051 conductive ground cord
B/W Printer Cleaning Sheet See printer user manual for requirements
Color Printer Cleaning Sheet See printer user manual for requirements
Disposable Gloves
1. Ask and Listen Ask the customer if they have any problems or questions about the
equipment.
2. Paperwork Fill in the top of Ultrasound Inspection Certificate (see Figure 10-8 on
page 10-41). Record all probes and Ultrasound system options.
3. Power up • Turn the Ultrasound 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.
• Where applicable, confirm that the battery is charged. If no AC Input
present, use the internal battery.
4. Probes Verify that the Ultrasound system properly recognizes all probes.
7. Review Error Logs Where applicable, Error Logs can be reviewed via system diagnostics.
8. Diagnostics Optional.
10. Image Archive Back up the Image Archive onto appropriate media.
1. B-Mode Verify basic B-Mode (2D) operation. Check the basic Ultrasound system
controls that affect this mode of operation.
2. CF-Mode Verify basic CF-Mode (Color Flow Mode) operation. Check the basic
Ultrasound system controls that affect this mode of operation.
3. Doppler Modes Verify basic Doppler operation (PW and CW if available). Check the basic
Ultrasound system controls that affect this mode of operation.
4. M-Mode Verify basic M-Mode operation. Check the basic Ultrasound system
controls that affect this mode of operation.
5. Probe Elements Perform an Element Test on each probe to verify that all the probe
elements and system channels are functional.
6. Applicable Verify the basic operation of all optional modes such as Contrast. Check
Software Options the basic Ultrasound system controls that affect each options operation.
7. Xmit/Recv Use the Visual Channel Utility on the loop connect to verify that all system
Elements xmit/recv channels are functional.
10. LCD Verify basic LCD display functions. Refer to Chapter 3 of the User Manual.
11. Software Menu Verify Software Menu display functions. Refer to Chapter 3 of the User
check Manual.
13. Measurements In measurement mode, make distance measurement, get result in result
window. Verify the distance by graduate rule. Distance Accuracy should
be within ±5%. (Name result from result window Result A, result from
graduate rule Result B; Distance Accuracy = (Result B-Result A)/Result A)
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.
7. DVD Verify that the DVD is functioning properly. Clean heads and covers if
necessary.
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.
10-6-2-4 Cleaning
1. Console Remove the battery. Use a fluid detergent in warm water on a soft, 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.
2. Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).
3. LCD Use a soft, non-abrasive folder cloth. Gently wipe the LCD face. DO NOT
use a glass cleaner that has a hydrocarbon base (such as Benzene,
Methy Alcohol or Methy Ethyl Ketone) on LCD with the filter (anti-glare
shield).
1. Labeling Verify that all Ultrasound system labeling is present and in readable
condition.
2. Scratches & Dents Inspect the exterior for dents, scratches or cracks. .
3. Input Power Refer to: 10-6-2-3 ‘Mains cable inspection’ on page 10-14.
4. Cables & Check all internal cable harnesses and connectors for wear and secure
Connectors connector seating. Pay special attention to footswitch assembly and probe
strain or bend reliefs.
5. Shielding & Check to ensure that all EMI shielding, internal covers, air flow panels and
Covers screws are in place. Missing covers and hardware could cause EMI/RFI
problems while scanning.
6. Control Panel Inspect keyboard and control panel. Note any damaged or missing items.
7. Control Panel Check for proper operation of all operator panel and Freeze Key light.
Lighting
8. LCD 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.
10. Power and Check for proper operation of all Power and System Status Indicators.
System Status
Indicators
11. 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,
1. Clean the probe holders with warm water and a damp cloth
to remove all traces of gel.
2. In the event that disinfection is required or any stubborn
stains remain, absorb a small quantity of isopropyl rubbing
alcohol on a soft, dust-free cloth. Wipe the surface of the
probe holder. Make sure no liquid drips into the system.
Allow to dry.
System cabinet
10-6-5-4 Footswitch
Clean the system's air filters to ensure that a clogged filter does
not cause the system to overheat and reduce system
performance and reliability. It is recommended the filters be
cleaned every two weeks, but the requirements will vary due to
your system use.
CAUTION Be sure to lock the wheels before cleaning the air filters to
avoid injury by any unexpected movement of the system.
DO NOT operate the unit without the air filters in place.
Allow the air filters to dry thoroughly before re-installing them
on the unit.
CAUTION Be sure to lock the wheels before cleaning the metal filter to
avoid injury by any unexpected movement of the system.
DO NOT operate the unit without the metal filter in place.
Allow the metal filter to dry thoroughly before re-installing them
on the unit.
2. Pull out the metal filter. The metal filter is located under the
air filter at the bottom of the system.
Put the hand under the bottom of the system and and use
fingers to slide out the metal filter slowly, then use the hand
to pull it out.
1. Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).
2. 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.
3. Probes Verify that the Ultrasound system properly recognizes all probes.
CAUTION Disinfect a defective probe before you return it. Be sure to tag
the probe as being disinfected.
WARNING Energy Control and Power Lockout for Vivid T8/Vivid T8 Pro.
When servicing parts of the Ultrasound system where there is
exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
6. Remove/disconnect the battery, if present.
Ultrasound System components may be energized.
Normal Reverse
Country Condition Open Ground Polarity Open Neutral
Table 10-13: Type BF Applied Part Leakage Current Limits - Probes Surface
NOTE: *Mains Applied refers to the sink leakage test where mains
(supply) voltage is applied to the part to determine the amount of
current that will pass (or sink) to ground if a patient contacted
mains voltage.
The following tests are performed at the factory and should be
performed at the site. These tests are: chassis leakage current,
and probe leakage current. All measurements are made with an
electrical safety analyzer which should be calibrated and
compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.
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. GROUND PIN
2. OHMMETER
3. Vivid T8/Vivid T8 Pro
4. ACCESSIBLE METAL PART:
• MONITOR HOUSING
• PEAR PANEL CONNECTOR
• ANY CASTER/WHEEL SUPPORT
The test verifies the isolation of the power line from the chassis.
The testing meter is connected from accessible metal parts of
the case to ground. Measurements should be made with the unit
ON and OFF, with the power line polarity Normal and Reversed.
Record the highest reading of current.
Figure 10-6. Set Up for Chassis Source Leakage Current, IEC 601-1 Clause 19 -
Continuos Leakage Currents and Patient, Auxiliary Currents
The test passes when all readings measure less than the value
shown in Table 10-12 on page 10-30. Record all data on the PM
Inspection Certificate.
Table 10-16: Typical Data Sheet for enclosure Source Leakage Current
Tester
Neutral
Tester or Test 1 Test 2 Real
Unit Polarity Ground Speaker Panel Metal Optional Optional
Power Switch Switch Cover Parts Test 3 Test 4
ON NORM OPEN
ON NORM CLOSED
ON REV OPEN
ON REV CLOSED
10-7-6-1 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: Some leakage current is expected on each probe, depending 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.
10-7-6-2 Tools
CONSOLE
POWER N (WHITE)
OUTLET
G (GREEN)
MOMENTARY
SWITCH LEAKAGE TEST
METER
The test passes when all readings measure less than the values
shown in Table 10-13 on page 10-30. Record all data on the PM
Inspection Certificate.
Table 10-17: Typical Data Sheet For Transducer Source Leakage Current
Transducer Tested:
ON NORM OPEN
ON NORM CLOSED
ON REV OPEN
ON REV CLOSED
* Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other
A pplic a ble H a rdwa re O ptions L a be ling (see User Manual for Labeling)
Control Panel
LCD
Measurement Accuracy
GE Approved Peripherals
COMMENTS:
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
ELECTRICAL SAFETY
Max Value Value
Electrical Test Performed Allowed Measured OK? Comments
PROBES
Probe 1:
Probe 2:
Probe 3:
Final Check. All system covers are in place. System scans with all probes as expected.
System ground
continuity
Chassis source
leakage current -
probe
Chassis source
leakage current -
wheel
Chassis source
leakage current -
monitor
Peripheral 1 leakage
current
Peripheral 1 ground
continuity
Peripheral 2 leakage
current
Peripheral 2 ground
continuity
Peripheral 3 leakage
current
Peripheral 3 ground
continuity
A verification, 3-18
customer provided prerequisite, 8-178
abbrevations, 9-3
acclimate time, 2-3 D
authorized representative in EU, 1-34
average setup time, 3-3 damage
in transportation, 3-11
B damage in transport, i-16
dangerous procedure warnings, 1-26
before installation (site preparations), 2-1 data network setup requirements, 2-18
Boot Up, 3-23 desirable features, 2-15
DICOM network function, 2-19
C DICOM setup requirements, 2-20, 2-22
display PDF files
cable inspection from manual CD-ROM
mains cable inspection, 10-14 print PDF files
care and maintenance, 10-1 from manual CD-ROM, 4-20
warnings, 10-3 disposal
CE compliance, 1-30 used media, 8-239
change history, i-1 used parts, 8-239
chapter 1
introduction, 1-1 E
chassis leakage current test, 10-34
Cleaning electrical requirements, 2-6
Ultrasound unit, 10-17 EMI limitations
cold or hot EMI limitations, 2-9
if the unit is very cold or hot, 2-3 general requirements, 2-6
compatibility site circuit breaker
hardware/software, 9-4 site circuit breaker, 2-7
completing the setup, 3-19 site power outlets
compliance, 1-30 site power outlets, 2-7
configuration, 3-24 specific requirements for the unit, 2-6
connect unit power plug
ethernet, 3-21 unit power plug, 2-7
probe, 3-23 electrical safety, 1-24
USB flash card, 3-21 electrical safety tests, 10-28
connections electrical specification, 3-20
on the rear panel, 3-21 electromagnetic interference
console environmental requirements, 2-3 abatement, 2-10
console requirements, 2-3 prevention, 2-10
contact information, 1-32 electrostatic discharge prevention, 1-31
contents in this manual, 1-3 EMC, 1-30
conventions used in book, 1-11 compliance, 1-30
cooling, 2-5 what is EMC?, 1-30
copyrights, i-19 EMI, 1-30
customer assistance, 1-32 abatement, 2-10
phone numbers, 1-33 prevention, 2-10
customer order protection, 3-18
G N
GE Healthcare leakage current limits, 10-30 network setup requirements, 2-18
general console requirements, 2-3
generic procedure on probe leakage current, 10-37 O
grounding continuity, 10-33
omission and errors, i-17
H operational and storage temperature for probes, 2-11
safety U
human, 1-18
safety precaution messages, 1-12 unpacking, 3-6
safety test overview, 10-28 unpacking instructions, 3-12
service safety considerations, i-18 USB
setup flash card
completion, 3-19 connect, 3-21
preparations, 3-18 used media
reminders, 3-3 disposal, 8-239
setup time, 3-3 used parts
setup warnings, 3-3 disposal, 8-239
shipping/returning probes and repair parts, 1-28
shock and tilt indicators V
position, 3-9
verification
W
warnings, 10-3
dangerous procedures, 1-26
receiving and unpacking, 3-6
what is EMC?, 1-30
when there’s too much leakage current, 10-39
chassis fails, 10-39
ECG fails, 10-40
new unit, 10-40
peripheral fails, 10-40
probe fails, 10-40
still fails, 10-40