IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
IMPORTANT PRECAUTIONS
• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN
ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.
WARNING
AVERTISSEMENT
• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE
MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.
• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE
PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL
OR OTHER HAZARDS.
• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.
• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE
LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE
TRADUIRE.
• NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE
MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.
• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE
TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES
DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.
WARNUNG
• DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER
SPRACHE.
• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT, IST
ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG ZU
SORGEN.
• VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN
WURDE.
• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN
DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN
DURCH ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.
i
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
• ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.
• SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA
QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCIÓN.
• NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER
AV I S O
CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.
• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL
PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN
LESIONES PROVOCADAS POR CAUSAS ELÉCTRICAS, MECÁNICAS O DE OTRA
NATURALEZA.
• ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM
INGLÊS.
• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A
GEMS, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.
ATENÇÃO
• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.
• O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.
AVVERTENZA
• IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN
INGLESE.
• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.
• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO
AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL
CONTENUTO.
• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR
COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA
MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE
ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.
ii
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
iii
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
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.
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY
All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the
equipment shall be performed by licensed electrical contractors. Other connections between pieces of
electrical equipment, calibrations and testing shall be performed by qualified GE Medical Systems
personnel. In performing all electrical work on these products, GE will use its own specially trained field
engineers. All of GE’s electrical work on these products will comply with the requirements of the
applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to perform
electrical servicing on the equipment.
OMISSIONS & ERRORS
If there are any omissions, errors or suggestions for improving this documentation, please contact the
GE Medical Systems Global Documentation Group with specific information listing the system type,
manual title, part number, revision number, page number and suggestion details. Mail the information
to: Service Documentation, 4855 W. Electric Ave (EA-53), Milwaukee, WI 53219, USA.
GE Medical Systems employees should use the iTrak System to report all documentation errors or
omissions.
iv
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
LEGAL NOTES
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without
prior written permission of GE Medical Systems.
GE Medical Systems may revise this publication from time to time without written notice.
TRADEMARKS
All products and their name brands are trademarks of their respective holders.
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
Chapter 1
Introduction
Section 1-1
Overview
1-1-1Purpose of Chapter 1
This chapter describes important issues related to safely servicing the Vivid™ 3 scanner. The service
provider must read and understand all the information presented here before installing or servicing a
unit.
Table 1-1 Contents in Chapter 1
SectionDescriptionPage Number
1-1
1-2
1-4
1-3
1-5
1-6
Overview
Important Conventions
Product Labels and Icons
Safety Considerations
EMC, EMI, and ESD
Customer Assistance
1-1-2Purpose of Service Manual
This manual provides installation and service information for the Vivid™ 3 ultrasound unit, and contains
the following chapters:
•Chapter 1 - Introduction:
Contains a content summary and warnings.
•Chapter 2 - Pre-Installation
Contains pre-installation requirements for the Vivid™ 3 ultrasound unit.
•Chapter 3 - Installation
Contains installation procedures and an installation checklist.
•Chapter 4 - Functional Checks
Contains functional checks that are recommended as part of the installation procedure, or as
required during servicing and periodic maintenance.
1-1
1-6
1-11
1-8
1-25
1-27
•Chapter 5 - Components and Function (Theory)
Contains block diagrams and functional explanations of the electronic circuits.
•Chapter 6 - Service Adjustments
Contains instructions for performing service adjustments to the Vivid™ 3 ultrasound unit.
•Chapter 7 - Diagnostics/Troubleshooting
Provides instructions for setting up and running diagnostic, troubleshooting and other related
routines for the Vivid™ 3 ultrasound unit.
Chapter 1 - Introduction 1-1
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
•Chapter 8 - Replacement Procedures
Provides disassembly and reassembly procedures for all Field Replaceable Units (FRUs).
•Chapter 9 - Renewal Parts
Contains a complete list of field replaceable parts for the Vivid™ 3 ultrasound unit.
•Chapter 10 - Periodic Maintenance
Provides periodic maintenance procedures for the Vivid™ 3 ultrasound unit.
1-1-3Typical Users of the Basic Service Manual
This manual is intended for the following categories of users:
•GE service personnel (installation, maintenance, etc.).
•Hospital service personnel.
•Contractors (some parts of Chapter 2 - Pre-Installation).
1-2Section 1-1 - Overview
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
1-1-4Vivid™ 3 Models Covered in this Manual
The Vivid™ 3models documented in this manual are shown in Tab le 1 -2 and Ta bl e 1- 3 below.
NOTE:The difference between the two types of Vivid™ 3 BTO3 models are as follows:
On RFI models (supported by software version 3.2, and above), Image Port, RFT, and FEC functionality
are all incorporated into one board - the RFI board.
For RFT models (supported by software versions below 3.2), the Image Port, RFT, and FEC boards are
all separate components.
Table 1-2 Vivid™ 3 - BT03 - RFI Models
ModelCat No.DescriptionComments
BASE Vivid 3 Console
Vivid 3 BT03
console, 220-240V AC, RFI
Vivid 3 BT03
console, 100V AC, RFI
Vivid 3 BT03
console, 110-120V AC, RFI
Vivid 3 BT03
console, 220-230V AC / NTSC, RFI
Vivid 3 BT03 console, NTRL, RFIH45521JB
H45011GD
H45011GE
H45011GF
H45011GG
An advanced version of the newer
generation of the Vivid™ 3 BT03
Ultrasound Scanning System.
Enables a larger variety of probes
and larger application use.
The BT03 is backward compatible to its
parallel product, the BT02 Pro and Expert
and its predecessor BT01 Pro and Expert.
Contact your local distributor for more
information about upgrades and backward
compatibility. BT00 hardware cannot be
upgraded to this level.
PRO Console
Vivid 3 BT03 PRO console, 220-240V AC, RFI H45011G
Vivid 3 BT03 PRO console, 100V AC, RFIH45011GA
Vivid 3 BT03 PRO console, 110-120V AC, RFI H45011GB
Vivid 3 BT03 PRO console, 220V-230V AC
/ NTSC, RFI
Vivid 3 BT03 PRO console, NTRL, RFIH45521JA
H45011GC
New generation of the Vivid™ 3
Ultrasound Scanning System,
continuation of the product line of
Vivid™ 3 BT01 & BT02. For global
universal use.
The Pro is backward compatible to its
predecessor, the BT01 & BT02.
Contact your local distributor for more
information about upgrades and backward
compatibility. BT00 hardware cannot be
upgraded to this level
Chapter 1 - Introduction 1-3
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
Table 1-3 Vivid™ 3 - BT03 - RFT Models
ModelCat No.DescriptionComments
BASE Vivid 3 Console
Vivid 3 BT03
console, 220-240V AC
Vivid 3 BT03
console, 100V AC
Vivid 3 BT03
console, 110-120V AC
Vivid 3 BT03
console, 220-230V AC / NTSC
Vivid 3 BT03 console, NTRLH45521EW
PRO Console
Vivid 3 BT03 PRO console,
220-240V AC
Vivid 3 BT03 PRO console,
100V AC
Vivid 3 BT03 PRO console,
110-120V AC
Vivid 3 BT03 PRO console,
220V-230V AC / NTSC
Vivid 3 BT03 PRO console,
NTRL
H45011ES
H45011ET
H45011EU
H45011EV
H45011FD
H45011FE
H45011FF
H45011FG
H45521FH
An advanced version of the newer
generation of the Vivid™ 3 BT03
Ultrasound Scanning System.
Enables a larger variety of probes
and larger application use.
New generation of the Vivid™ 3
Ultrasound Scanning System,
continuation of the product line of
Vivid™ 3 BT01 & BT02. For global
universal use.
The BT03 is backward compatible to its
parallel product, the BT02 Pro and Expert
and its predecessor BT01 Pro and Expert.
Contact your local distributor for more
information about upgrades and backward
compatibility. BT00 hardware cannot be
upgraded to this level.
The Pro is backward compatible to its
predecessor, the BT01 & BT02.
Contact your local distributor for more
information about upgrades and backward
compatibility. BT00 hardware cannot be
upgraded to this level
NOTE:Vivid™ 3 systems with Serial No 5000 and above, have the RFI system hardware configuration. All
systems with a serial number prior to this (i.e. 4999 and below) are configured with RFT hardware.
1-4Section 1-1 - Overview
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
1-1-5System History - Hardware and Software Versions
The newest generation of the Vivid™ 3 (BT03) ultrasound unit is based on its predecessor, the
Vivid™ 3 (BT01 and BT02) ultrasound unit, and is therefore backward compatible. The Vivid™ 3
ultrasound unit enables advanced features in a compact and user friendly tool.
Note:Vivid™ 3 (BT00) cannot be upgraded to the Vivid™ 3 Pro 03 as was the case for Pro 02.
The Vivid™ 3 Pro and Vivid™ 3 are the same generation of products, but differ in their functionality,
enabling customers to receive some of the advanced Vivid™ 3 features. With minor software and hardware
modifications, the Vivid™ 3 Pro can be upgraded to the Vivid™ 3 - refer to Ta bl e 1 -4 .
Table 1-4 Vivid™ 3 Upgrade Options Available
Part No.UpgradeComments
H45011BABT00 to BT00 Pro upgrade
H45011BPBT00 to BT00 Pro upgrade for P509 probe
H45011BCPlatform upgrade from Vivid™ 3 BT01 "Pro" to "Expert"
H45011DLBT00 to Pro-02 upgrade
H45011DMBT00 Pro to Pro-02 upgrade
H45011DRBT01 Pro to Pro-02 upgrade
H45011DSBT01 Expert to Expert -02 upgrade
H45011FBBT01/BT02 Pro to BT03 UpgradeNew
H45011FCBT01/BT02 Expert to BT03 UpgradeNew
H45011BN3rd Probe Connector for Vivid 3 system field upgradeNew
H45011MK17 " Monitor field upgradeNew
1-1-6Purpose of Operator Manual(s)
The Operator Manual(s) should be fully read and understood before operating the Vivid™ 3 system, and also
kept near the unit for quick reference.
Chapter 1 - Introduction 1-5
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
Section 1-2
Important Conventions
1-2-1Conventions Used in this Manual
1-2-1-1Model Designations
This manual covers the Vivid™ 3 ultrasound units listed in Table 1-2 on page 1-3 and Table 1-3 on
page 1-4.
1-2-1-2Icons
Pictures, or icons, are used wherever they will reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.
1-2-1-3Safety Precaution Messages
Various levels of safety precautions are found on the equipment and throughout this service manual.
Different levels of severity are identified by one of the following icons which precede precautionary
statements in the text.
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 the instructions are ignored.
CAUTION: Indicates the presence of a hazard that can cause property damage but has absolutely no
personal injury risk.
Note:Notes are used to provide important information about an item or a procedure. Be sure to read
the notes as the information they contain can often save you time or effort.
1-6Section 1-2 - Important Conventions
GE MEDICAL SYSTEMS
IRECTION 2300164-100, REVISION 7VIVID™ 3 PRO/VIVID™ 3 SERVICE MANUAL
D
1-2-1-4Standard Hazard Icons
Important information will always 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.
Table 1-5 Standard Hazard Icons
ELECTRICALMECHANICALRADIATION
LASERHEATPINCH
LASER
LASER
LIGHT
LIGHT
Other hazard icons make you aware of specific procedures that should be followed.
Table 1-6 Standard Icons Indicating a Special Procedure Be Used
AVOID STATIC ELECTRICITYTAG AND LOCK OUTWEAR EYE PROTECTION
TAG
TAG
&
&
LOCKOUT
LOCKOUT
Date
Signed
EYE
EYE
PROTECTION
PROTECTION
Chapter 1 - Introduction 1-7
Loading...
+ 600 hidden pages
You need points to download manuals.
1 point = 1 manual.
You can buy points or you can get point for every manual you upload.