IRECTION 2392751-100, REVISION 3VIVID™ 4 SERVICE MANUAL
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.
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• 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.
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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.
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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 2392751-100, REVISION 3VIVID™ 4 SERVICE MANUAL
Chapter 1
Introduction
Section 1-1
Overview
1-1-1Purpose of Chapter 1
This chapter describes important issues related to safely servicing the Vivid™ 4 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™ 4 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™ 4 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
1-5
1-10
1-7
1-24
1-26
•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™ 4 ultrasound unit.
•Chapter 7 - Diagnostics/Troubleshooting
Provides instructions for setting up and running diagnostic, troubleshooting and other related
routines for the Vivid™ 4 ultrasound unit.
Chapter 1 - Introduction 1-1
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•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™ 4 ultrasound unit.
•Chapter 10 - Periodic Maintenance
Provides periodic maintenance procedures for the Vivid™ 4 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
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1-1-4Vivid™ 4 Models Covered in this Manual
The Vivid™ 4models 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™ 4 BT03 models are as follows:
On RFI models (supported by software version 4.2, 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 4.2), the Image Port, RFT, and FEC boards are
all separate components.
Table 1-2 Vivid™ 4 BT03 - RFI Models
ModelCat No.Description
BASE Vivid 4 Console
Vivid 4 BT03
console, 220-240V AC, RFI
Vivid 4 BT03
console, 100V AC, RFI
Vivid 4 BT03
console, 110-120V AC, RFI
Vivid 4 BT03
console, 220-230V AC / NTSC, RFI
Vivid 4 BT03 console, NTRL, RFIH45531JC
H45011FT
H45011FW
H45011FY
H45011FZ
An advanced version of the Ultrasound Scanning
Systems based on the Vivid product line. Enables a
larger variety of probes and larger application use.
Table 1-3 Vivid™ 4 BT03 - RFT Models
ModelCat No.Description
BASE Vivid 4 Console
Vivid 4 BT03
console, 220-240V AC
Vivid 4 BT03
console, 100V AC
Vivid 4 BT03
console, 110-120V AC
Vivid 4 BT03
console, 220-230V AC / NTSC
Vivid 4 BT03 console, NTRLH45531GC
H45011DT
H45011DU
H45011DV
H45011DW
An advanced version of the Ultrasound Scanning
Systems based on the Vivid product line. Enables a
larger variety of probes and larger application use.
NOTE:Vivid™ 4 systems with Serial No 10500 and above, have the RFI system hardware configuration. All
systems with a serial number prior to this (i.e. 10499 and below) are configured with RFT hardware.
Chapter 1 - Introduction 1-3
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1-1-5System History - Hardware and Software Versions
The newest generation of the Vivid™ 4 (BT03) ultrasound unit is based on the Vivid 3 (BT01 and BT02)
ultrasound unit, and therefore shares much of the same hardware. However, even though much of the
hardware is the same, the Vivid 3 cannot be upgraded to Vivid™ 4, or vice-versa. The Vivid™ 4
ultrasound unit provides advanced features, in a compact and user-friendly tool.
1-1-6Purpose of Operator Manual(s)
The Vivid™ 4 User Guide and Operator Manual(s) should be fully read and understood before operating the
Vivid™ 4 system, and also kept near the unit for quick reference.
1-4Section 1-1 - Overview
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Section 1-2
Important Conventions
1-2-1Conventions Used in this Manual
1-2-1-1Model Designations
This manual covers the Vivid™ 4 ultrasound units listed in Table 1-2 on page 1-3 and Table 1-3 on
page 1-3 .
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.
Chapter 1 - Introduction 1-5
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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 1-4 Standard Hazard Icons
ELECTRICALMECHANICALRADIATION
LASERHEATPINCH
LASER
LASER
LIGHT
LIGHT
Other hazard icons make you aware of specific procedures that should be followed.
Table 1-5 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
1-6Section 1-2 - Important Conventions
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Section 1-3
Safety Considerations
1-3-1Introduction
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.
1-3-2Human Safety
Operating personnel must not remove the system covers.
Servicing should be performed by authorized personnel only.
Only personnel who have participated in Vivid™ 4 Training are authorized to service the equipment.
1-3-3Mechanical Safety
DANGER: WHEN THE UNIT IS RAISED FOR A REPAIR OR MOVED ALONG ANY INCLINE,
USE EXTREME CAUTION SINCE IT MAY BECOME UNSTABLE AND TIP OVER.
DANGER: ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS
THAT CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN
HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A
DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN
RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.
DANGER: NEVER USE A PROBE THAT HAS BEEN SUBJECTED TO MECHANICAL
SHOCK OR IMPACT. EVEN IF THE PROBE APPEARS TO BE UNBROKEN, IT MAY IN
FACT BE DAMAGED.
CAUTION: Always lower and center the Operator I/O Panel before moving the scanner.
CAUTION: The Vivid™ 4 weighs 170 kg (375 lbs.) or more, depending on installed peripherals,
when ready for use. Care must be used when moving it or replacing its parts. Failure to follow
the precautions listed could result in injury, uncontrolled motion and costly damage.
ALWAYS:
Be sure the pathway is clear.
Use slow, careful motions.
Use two people when moving the system on inclines or lifting more than 16 kg (35 lbs). Also,
whenever lifting/removing the monitor, two people are required.
WARNING: Always lock the control console in its parking (locked) position after moving the
system. Failure to do so could result in personal injury or equipment damage.
Chapter 1 - Introduction 1-7
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WARNING: Equipment damage could result if special care is not taken when transporting the
system in a vehicle.
ALWAYS:
•Secure the system in an upright position and lock the wheels (brake).
•DO NOT use the control console as an anchor point.
•Place the probes in their carrying case.
•Eject any disks from the MOD (if installed).
•Ensure that the system is well prepared and packed in its original packaging before
transporting. Special care must be taken to correctly position the packing material
supporting the monitor. For further information, refer to Chapter 3 - Installation.
CAUTION: Keep the heat venting holes on the monitor unobstructed to avoid overheating of the
monitor.
1-3-4Electrical Safety
To minimize shock hazard, the equipment chassis must be connected to an electrical Ground. The
system is equipped with a three-conductor AC power cable. This must be plugged into an approved
electrical outlet with safety grounding.
The power outlet used for this equipment should not be shared with other types of equipment. Both the
system power cable and the power connector must meet international electrical standards.
Note:When replacing UPS batteries, ensure that defective batteries are disposed of in accordance
with local regulations. Alternatively, forward them to GE Medical Systems for proper disposal.
1-3-4-1Probes
All the probes for the Vivid™ 4 ultrasound unit 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 transducer elements,
acoustic lens, or housing.
•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.
•To avoid the risk of a probe accidentally falling, do not allow the probe cables to become entangled,
or to be caught in the machine’s wheels.
NOTE:For detailed information on handling endocavity probes, refer to the appropriate supplementary
instructions for each probe. In addition, refer to the Vivid™ 4 User Manual for detailed probe handling
instructions.
1-8Section 1-3 - Safety Considerations
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1-3-5Dangerous Procedure Warnings
Warnings, such as the examples below, precede potentially dangerous procedures throughout this
manual. Instructions contained in the warnings must be followed.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS
EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
EXPLOSION WARNING
DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.
OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A
DEFINITE SAFETY HAZARD.
DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT
BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT INSTALL
SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION OF THE
EQUIPMENT.
Chapter 1 - Introduction 1-9
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Section 1-4
Product Labels and Icons
The Vivid™ 4 ultrasound unit comes equipped with product labels and icons. These labels and icons
represent pertinent information regarding the operation of the ultrasound unit.
1-4-1Product Label Locations
The following two diagrams indicate the location of some of the labels and icons found on the Vivid™ 4
ultrasound unit. All the labels and icons are described in Table 1-6 on page 1-12.
1
2
3
Figure 1-1 Product Label and Icon Locations (Front)
1Product Logo
2Equipment Type CF
3Parking Label on Brake Pedal
4Class II Equipment
5Swivel Brake Label on Brake Pedal
1-10Section 1-4 - Product Labels and Icons
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1
2
3
Figure 1-2 Product Label and Icon Locations (Rear)
1 Main Label
2 AC Voltage Rating Label
3 GND Label
Chapter 1 - Introduction 1-11
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1-4-2Label Descriptions
The following table shows the labels and symbols that may be found on the Vivid™ 4 ultrasound unit,
and provides a description of each label’s purpose and location.
Table 1-6 Product Icons
Label NameDescriptionLocation
Product LogoIdentifies Vivid™ 4 models.Front of the unit.
Manufacturer’s name and address.
Identification and Rating
Plate
Date of Manufacture.
Model and Serial numbers.
Electrical ratings.
Class I Equipment, in which protection
against electric shock does not rely on basic
insulation only, but which includes an
additional safety precaution in that means
are provided for the connection of the
equipment to the protective earth conductor
in the fixed wiring of the installation - in such
a way that accessible metal parts cannot
become live in the event of a failure of the
basic insulation.
Rear of the unit, near the power inlet.
Rear of the unit and probe
connectors.
Device Listing/Certification
Labels
CAUTION - This machine
weighs...Special care must
be used to avoid..."
Laboratory logos or labels that denote
conformity with industry safety standards,
such as UL or IEC.
CE certification mark.Rear of the unit, on the main label.
Equipment Type BF (man in the box symbol)
IEC 878-02-03 indicates B Type equipment
having even more electrical isolation than
standard Type B equipment because it is
intended for intimate patient contact.
Equipment Type CF IEC 878-02-05
indicates equipment having a floating
applied part that provides a degree of
protection suitable for direct cardiac contact.
This precaution is intended to prevent injury
that may be caused by the weight of the
machine if one person attempts to move it
considerable distances or on an incline.
Rear of the unit.
Probe connectors
PCG connector
or Rear of Console
Front of the unit, ECG connector and
surgical probes.
Used in the Service and User Manual
which should be adjacent to
equipment at all times for quick
reference.
1-12Section 1-4 - Product Labels and Icons
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Table 1-6 Product Icons (Continued)
Label NameDescriptionLocation
"DANGER - Risk of explosion
used in..."
The system is not designed for use with
flammable anesthetic gases.
"CAUTION" The equilateral triangle is
usually used in combination with other
symbols to advise or warn the user.
“ATTENTION - Consult accompanying
documents” is intended to alert the user to
refer to the User Manual or other instructions
when complete information cannot be
provided on the label.
"CAUTION - Dangerous voltage" (the
lightning flash with arrowhead in equilateral
triangle) is used to indicate electric shock
hazards.
"Protective Earth" Indicates the protective
earth (grounding) terminal.
Indicated in the Service Manual.
Rear of the unit.
Rear of the unit.
Rear of the unit.
Rear of the unit.
"Equipotentiality" Indicates the terminal to be
used for connecting equipotential
conductors when interconnecting
(grounding) with other equipment.
Waste Electrical and Electronic Equipment
(WEEE) Disposal
This symbol indicates that the waste of
electrical and electronic equipment must not
be disposed as unsorted municipal waste
and must be collected separately.
Please contact an authorized representative
of the manufacturer for information
concerning the decommissioning of your
equipment.
Peripherals
Rear of the unit.
Chapter 1 - Introduction 1-13
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1-4-3Vivid™ 4 External Labels
In addition to the labels described in the previous section, additional labels may be found on the
Vivid™ 4 ultrasound unit, as described in the following sections:
•Main Label section, on page 1-14.
•Rating Labels section, on page 1-22.
•GND Label section, on page 1-23.
•Parking Label section, on page 1-23.
•Swivel Brake Label section, on page 1-23.
1-4-3-1Main Label
The main label may be printed in any of the following languages: English, German, French, Spanish,
Portuguese, Italian, Chinese, Danish, Dutch, Finnish, Greek, Japanese, Norwegian, Russian, or
Swedish, as shown in the examples below. Each main label includes a serial number, a voltage rating,
caution warnings, danger warnings and classifications (UL, CE0344 and so on.)
•English: Used for all countries except those in which German, French, Spanish, Portuguese or
Italian are spoken.
Figure 1-3 Main Label (English) 220 -240V
.
Figure 1-4 Main Label (English) USA
1-14Section 1-4 - Product Labels and Icons
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•German: Used in all German language countries.
Figure 1-5 Main Label (German)
•French: Used in all French language countries.
Figure 1-6 Main Label (French)
Chapter 1 - Introduction 1-15
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•Spanish: Used in all Spanish language countries.
Figure 1-7 Main Label (Spanish)
•Portuguese: Used in all Portuguese language countries.
Figure 1-8 Main Label (Portuguese)
1-16Section 1-4 - Product Labels and Icons
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Figure 1-9 Main Label (Portuguese) 220 - 240V
•Italian: Used in all Italian language countries.
Figure 1-10 Main Label (Italian)
Chapter 1 - Introduction 1-17
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•Chinese: Used in all Chinese language countries.
Figure 1-11 Main Label (Chinese)
•Danish: Used in all Danish language countries.
Figure 1-12 Main Label (Danish)
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•Dutch: Used in all Dutch language countries.
Figure 1-13 Main Label (Dutch)
•Finnish: Used in all Finnish language countries.
Figure 1-14 Main Label (Finnish)
Chapter 1 - Introduction 1-19
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•Greek: Used in all Greek language countries.
Figure 1-15 Main Label (Greek)
•Japanese: Used in all Japanese language countries.
Figure 1-16 Main Label (Japanese)
1-20Section 1-4 - Product Labels and Icons
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•Norwegian: Used in all Norwegian language countries.
Figure 1-17 Main Label (Norwegian)
•Russian: Used in all Russian language countries.
Figure 1-18 Main Label (Russian)
Chapter 1 - Introduction 1-21
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•Swedish: Used in all Swedish language countries.
Figure 1-19 Main Label (Swedish)
1-4-3-2Rating Labels
Indicates the ultrasound unit’s factory preset input AC voltage as follows:
•AC 100V
•AC 120V
•AC 220-240V
•AC 220-230V
One of the rating labels (shown in Figure 1-20 below) is located on the rear of the ultrasound unit.
Figure 1-20 Rating Labels
1-22Section 1-4 - Product Labels and Icons
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1-4-3-3GND Label
Indicates the protective earth (grounding) terminal. The GND label shown below is located at the rear
of the unit, as shown in Figure 1-2 on page 1-11.
Figure 1-21 GND Label
1-4-3-4Parking Label
Indicates the locked pedal position which locks the front castors and prevents the ultrasound unit from
moving. The parking label, shown below, is located on the brake pedal at the front of the unit, as shown
in Figure 1-1 on page 1-10.
Figure 1-22 Parking Label
1-4-3-5Swivel Brake Label
Indicates the locked swivel position which prevents the front castors from swiveling. The swivel brake
label, shown below, is located on the brake pedal at the front of the unit, as shown in Figure 1-1 on
page 1-10.
Figure 1-23 Swivel Break Label
Chapter 1 - Introduction 1-23
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Section 1-5
EMC, EMI, and ESD
1-5-1Electromagnetic Compatibility (EMC)
Electromagnetic compatibility describes a level of performance of a device within its electromagnetic
environment. This environment consists of the device itself and its surroundings, including other
equipment, power sources and persons with which the device must interface. Inadequate compatibility
results when a susceptible device fails to perform as intended due to interference from its environment,
or when the device produces unacceptable levels of emission. This interference is often referred to as
radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through space or
conducted over interconnecting power or signal cables. In addition to electromagnetic energy, EMC
also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and
disturbances in the electrical power supply.
1-5-2Electrostatic Discharge (ESD) Prevention
CAUTION: DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO
TAKING THE NECESSARY ESD PRECAUTIONS:
1.ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED ESD
CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (TO THE RIGHT OF
THE POWER CONNECTOR).
2.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE
EQUIPMENT.
1-24Section 1-5 - EMC, EMI, and ESD
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1-5-3Standards Used
To fulfill the requirements of relevant EC directives and/or European Harmonized/International
standards, the following documents/standards have been used:
Table 1-7 Standards Used
Standard/DirectiveScope
89/336/EECEMC Directive.
93/42/EECMedical Device Directive.
IEC 801-2Electrostatic Discharge.
IEC 801-3Radiated Electromagnetic Field.
IEC 801-4Electrical Fast Transient/Burst.
IEC 805-1Surge.
EN 55011/CISPR 11Electromagnetic Susceptibility.
EN 60601-1/IEC 601-1/UL 2601-1Medical Electrical Equipment; General Requirements for Safety.
EN 61157/ IEC 61157
Requirements for the declaration of the acoustic output of medical
diagnostic ultrasonic equipment.
NOTE:For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh and clamps are in good
condition and 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.
1-5-4Lockout/Tagout Requirements (For USA Only)
Follow OSHA Lockout/Tagout requirements by ensuring you are in total control of the electrical
Mains plug.
Chapter 1 - Introduction 1-25
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Section 1-6
Customer Assistance
1-6-1Contact Information
If this equipment does not work as indicated in this service manual or in the Vivid™ 4 User Manual, or
if you require additional assistance, please contact the local distributor or appropriate support resource,
as listed below.
Prepare the following information before you call:
•System ID and/or serial number.
•Software version.
Table 1-8 GE Contact Information
LocationPhone Number
USA/ Canada
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center
Latin America
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center
Europe
GE Ultraschall Deutschland GmbH& Co. KG
BeethovenstraBe 239
Postfach 11 05 60, D-42665 Solingen
Germany
Asia (Singapore/ Japan)
GE Ultrasound Asia
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Central Plaza
Singapore 169730
Phone: +1-800-437-1171
Phone: +1-800-321-7937
Phone: +1-800-682-5327
Phone: +1-262-524-5698
Fax:+1-414-647-4125
Phone: +1-262-524-5300
Phone: +1-262-524-5698
Fax:+1-414-647-4125
General Imaging: +49 (212) 2802 207
Cardiac:+49 (212) 2802 208
Fax:+49 212 2802 431
Phone:+65-277-3487
Fax:+65-272-3997
Phone: +81-426-48-2950
Fax:+81-426-48-2902
1-26Section 1-6 - Customer Assistance
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Chapter 2
Pre-Installation
Section 2-1
Overview
2-1-1Purpose of Chapter 2
This chapter provides the information required to plan and prepare for the installation of a Vivid™ 4
ultrasound unit. Included are descriptions of the electrical and facility requirements that must be met by
the purchaser. A worksheet is provided at the end of this chapter (see Figure 2-2 on page 2-11) to help
ensure that all the required network information is available, prior to installation.
Table 2-1 Contents in Chapter 2
SectionDescriptionPage Number
2-1
2-2
2-3
Overview
Console Requirements
Facility Needs
2-1
2-2
2-7
Chapter 2 - Pre-Installation 2-1
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Section 2-2
Console Requirements
2-2-1Unit Environmental Requirements
Table 2-2 Environmental Requirements
Relative Humidity
RequirementTemperature
(non-condensing)
Air Pressure
Operational
Storage
Transport
10 — 40
-20 — 60
-20 — 60
o
C(50 — 104oF)
o
C(-4 — 140oF)
o
C(-4 — 140oF)
50 — 70%700 — 1060 hPa
10 — 95%700 — 1060 hPa
10 — 95%700— 1060 hPa
CAUTION: If the system has been in storage or has been transported, please see the acclimation
requirements before powering
ON and/or using the system. Refer to the Installation Warnings section
on page 3-2.
2-2-2Cooling Requirements
The cooling requirement for the Vivid™ 4 ultrasound unit environment is
3500 BTU/hr. This figure does not include the cooling required for lights, people, or other equipment in
the room.
Note:Each person in the room places an additional 300 BTU/hr demand on the environmental cooling.
2-2-3Lighting Requirements
For system installation, updates and repairs, bright lighting is required. However, operator and patient
comfort may be optimized if the room lighting is subdued and indirect when a scan is being performed.
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.
2-2-4Time and Manpower Requirements
Site preparation takes time. Begin pre-installation checks as soon as possible to allow sufficient time to
make any required changes. If possible, begin these checks as many as six weeks before system
delivery.
CAUTION: At least two people must be available to deliver and unpack the Vivid™ 4 ultrasound
unit. Attempts to move the unit considerable distances (or on an incline) by one person alone,
could result in personal injury, and/or damage to the system.
2-2Section 2-2 - Console Requirements
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2-2-5Electrical Requirements
NOTE:GE Medical Systems 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.
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 unit is only a conduit.
2-2-5-1Vivid™ 4 Power Requirements
Electrical specifications for the Vivid™ 4 monitor and onboard peripherals are as follows:
Table 2-3 Electrical Requirements
VoltageTolerancesOp. CurrentFrequency
100V AC±10%8A50-60 Hz
120V AC±10%8A50-60 Hz
220 - 240V AC±10%4A50-60 Hz
2-2-5-2Inrush Current
Inrush current is not a factor for consideration, due to the inrush current limiting properties of the power
supplies.
Maximum power requirement = 1.2 KVa
•100V AC: 8A
•120V AC: 8A
•220 - 240V AC: 4A
2-2-5-3Site Circuit Breaker
It is recommended that the branch circuit breaker for the machine be readily accessible.
CAUTION
POWER OUTAGE MAY OCCUR.
The Vivid 3 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.
Chapter 2 - Pre-Installation 2-3
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2-2-5-4Site Power Outlets
A dedicated AC power outlet must be within reach of the unit without requiring the use of extension
cords. Other outlets adequate for the external peripherals, medical and test equipment required to
support this unit must also be present and located within 1 m (3.2 ft) of the unit. Electrical installation
must meet all current local, state, and national electrical codes.
2-2-5-5Mains Power Plug
If the unit arrives without a power plug, or with the wrong plug, contact your GE dealer. When necessary,
the installation engineer will supply the locally-required power plug.
2-2-5-6Power Stability Requirements
Voltage drop-out
Max 10 ms.
NOTE:The Vivid™ 4 ultrasound unit can be provided with an external UPS system. Contact your local
GE Service Representative for details.
Power Transients
(All applications)
Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including
line frequency, synchronous, asynchronous, or aperiodic transients.
2-4Section 2-2 - Console Requirements
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2-2-6EMI Limitations
Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transients in the air or wiring. They also generate EMI. The Vivid™ 4 ultrasound
unit 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 unit is installed, and should not be on the
same line as the ultrasound system. A dedicated line should be used for the ultrasound system.
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 ovens.
•Portable phones.
•Broadcast stations and mobile broadcasting machines.
Chapter 2 - Pre-Installation 2-5
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The following table lists recommendations for preventing EMI:
Table 2-4 EMI Prevention/ Abatement
EMI RuleDetails
Ground the unit.
Be aware of RF sources.
Replace and/or reassemble all
screws, RF gaskets, covers and
cores.
Replace broken RF gaskets.
Do not place labels where
RF gaskets touch metal.
Use GE specified harnesses and
peripherals.
Take care with cellular phones.Cellular phones may transmit a 5 V/m signal that causes image artifacts.
Properly address peripheral cables.
Poor grounding is the most likely reason an ultrasound unit will have noisy images.
Check the grounding of the power cord and power outlet.
Keep the unit at least 5m (16.4 ft) away from other EMI sources. Special shielding may
be required to eliminate interference problems caused by high frequency, high
powered radio or video broadcast signals.
After you finish repairing or updating the system, replace all covers and tighten all
screws. Any cable with an external connection requires a magnet wrap at each end.
Install the shield over the front of the card cage. Loose or missing covers or RF gaskets
allow radio frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an RF gasket are broken, replace the
gasket. Do not turn ON the unit until any loose metallic part is removed and replaced,
if required.
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will
permit RF leakage. In case a label has been found in such a location, move the label
to a different, appropriate location.
The interconnect cables are grounded and require ferrite beads and other shielding.
Cable length, material, and routing are all important; do not make any changes that do
not meet all specifications.
Do not allow cables to lie across the top of the card cage or hang out of the peripheral
bays. Loop any peripheral cable excess length inside the peripheral bays or hang on
the hooks provided below the console. Attach the monitor cables to the frame.
2-2-7Probe Environmental Requirements
Table 2-5 Probe Operation and Storage Temperatures
ElectronicsPAMPTE
Operation
Storage
Note:System and electronic probes are designed for storage temperatures of -20o to +50o C. When
exposed to large temperature variations, the probes should be kept at room temperature for
a minimum of 10 hours before use.
2-6Section 2-2 - Console Requirements
10 — 40oC (50 — 104oF)5 — 42.7oC (41 — 109oF)
-20 — 50oC (-4 — 122oF)-20 — 50oC(-4 — 122oF)
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Section 2-3
Facility Needs
2-3-1Purchaser Responsibilities
The work and materials required to prepare the site are the responsibility of the purchaser. To avoid
delay, complete all pre-installation work before delivery. Use the Pre-installation Check List (provided
in Table 2-6 on page 2-12)to verify that all the required steps have been completed.
Purchaser responsibilities include:
•Procuring the required materials.
•Completing the preparations prior to delivery of the ultrasound system.
•Paying the costs of any alterations and modifications not specifically provided for in the sales
contract.
Note:All relevant preliminary electrical installations at the prepared site must be performed by
licensed electrical contractors. Other connections between electrical equipment, and
calibration 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 utilize only
qualified personnel to perform electrical servicing of the equipment.
To avoid delays during installation, the individual or team who will perform the installation should be
notified at the earliest possible date (preferably prior to installation), of the existence of any of the
following variances:
•Use of any non-listed product(s).
•Use of any customer provided product(s).
•Placement of an approved product further from the system than the interface kit allows.
The prepared site must be clean prior to delivery of the system. Carpeting is not recommended because
it collects dust and creates static. Potential sources of EMI should also be investigated before delivery.
Dirt, static, and EMI can negatively impact system reliability.
Chapter 2 - Pre-Installation 2-7
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2-3-2Mandatory Site Requirements
The following are mandatory site requirements. Additional (optional) recommendations, as well as a
recommended ultrasound room layout, are provided in section 2-3-3 - Site Recommendations (see
below).
•A dedicated single branch power outlet of adequate amperage (see Table 2-3 on page 2-3.) that
meets all local and national codes and is located less than 2.5 m (8.2 ft) from the unit’s proposed
location. Refer to the Electrical Requirements section on page 2-3.
•A door opening of at least 76 cm (2.5 ft) in width.
•The proposed location for the unit is at least 0.3 m (1 ft) from the walls, to enable cooling.
•Power outlets for other medical equipment and gel warmer.
•Power outlets for test equipment within 1 m (3.3 ft) of the ultrasound unit.
•Clean and protected space for storage of probes (either in their case or on a rack).
•Material to safely clean probes.
•In the case of a network option:
•An active network outlet in the vicinity of the ultrasound unit.
•A network cable of appropriate length (regular Pin-to-Pin network cable).
•An IT administrator who will assist in configuring the unit to work with your local network. A fixed
IP address is required. Refer to the form provided in Figure 2-2 on page 2-11 for network details
that are required.
Note:All relevant preliminary network outlets installations at the prepared site must be performed by
authorized contractors. The purchaser of GE equipment must utilize only qualified personnel to
perform servicing of the equipment.
2-3-3Site Recommendations
The following are (optional) site recommendations. Mandatory site requirements are provided in the
Mandatory Site Requirements section, above.
•A door opening of 92 cm (3 ft) in width.
•An accessible circuit breaker for a dedicated power outlet.
•A sink with hot and cold running water.
•A receptacle for bio–hazardous waste, for example, used probe sheaths.
•An emergency oxygen supply.
•A storage area for linens and equipment.
•A nearby waiting room, lavatory, and dressing room.
•Dual level lighting (bright and dim).
•A lockable cabinet for software and manuals.
2-8Section 2-3 - Facility Needs
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2-3-3-1Recommended Ultrasound Room Layout
VIVID 4
36 IN.
(92 CM)
Scale: Each square = 1 sq ft (144 sq ins)
Figure 2-1 Minimal Floor Plan 2.5m x 3m (8.2ft x 9.84 ft)
2-3-4Networking Pre-Installation Requirements
2-3-4-1Stand-alone Unit (without Network Connection)
None.
2-3-4-2Unit Connected to Hospital’s Network
Supported networks:
Dedicated Power Outlets
Hospital Network
Dedicated Analog Telephone Line
for Connection to InSite
GE Cabinet for
Software and Manuals
(optional)
•100/10 Mbit/sec
2-3-4-3Purpose of the DICOM Network Function
DICOM services provide the operator with clinically useful features for moving images and patient
information over a hospital network. Examples of DICOM services include the transfer of images to
workstations for viewing or transferring images to remote printers. As an added benefit, transferring
images in this manner frees up the on-board monitor and peripherals, enabling viewing to be done while
scanning continues. With DICOM, images can be archived and stored faster, easier, and at a lower cost.
Chapter 2 - Pre-Installation 2-9
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2-3-4-4DICOM Option Pre-Installation Requirements
To configure the Vivid™ 4 ultrasound unit to work with other network connections, the network
administrator must provide the required information, which should include the following:
•Vivid™ 4 Details: DICOM network details for the Vivid™ 4 unit, including the host name, local port,
IP address, AE title and net mask.
•Routing Information: IP addresses for the default gateway and other routers in use at the site.
•DICOM Application Information: Details of the DICOM devices in use at the site, including the
DICOM host name, AE title and IP addresses.
2-10Section 2-3 - Facility Needs
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Section 2-4
Connectivity Installation Worksheet
Site System Information
Site:
Dept:
Vivid™ 4 SN:
CONTACT INFORMATION
Name
TCP/IP Settings
Scanner IP Settings
Name - AE Title:
IP Address:
Subnet Mask:
Default Gateway:
Type:
Title
Floor:
Room:
REV:
Phone
Comments:
E-Mail Address
Remote Archive Setup
(Echo Server/GEMNet Server/EchoPac PC)
Name - AE Title:
IP Address:
Subnet Mask:
Default Gateway:
Server Name:
Remote DB User Name:
Services (Destination Devices)
Device Type
1
2
3
4
5
6
7
8
9
10
11
12
Manufacturer
Figure 2-2 Connectivity Installation Worksheet
Name
IP Address
Port
AE Title
Chapter 2 - Pre-Installation 2-11
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Table 2-6 Pre-Installation Check List
ActionYesNo
Schedule at least 3 hours for installation of the system.
Notify installation team of the existence of any variances from the basic installation.
Make sure system and probes have been subject to acclimation period.
Environmental cooling is sufficient.
Lighting is adjustable to adapt to varying operational conditions of the scanner.
Electrical facilities meet system requirements.
EMI precautions have been taken and all possible sources of interference have been
removed.
Mandatory site requirements have been met.
If a network is used, IP address has been set for the system and a dedicated network
outlet is available.
IRECTION 2392751-100, REVISION 3VIVID™ 4 SERVICE MANUAL
Chapter 3
Installation
Section 3-1
Overview
3-1-1Purpose of Chapter 3
This chapter provides instructions for installing the Vivid™ 4 ultrasound unit. Before beginning the
installation process, an appropriate site must be prepared, as described in Chapter 2 - Pre-Installation.
Once the site has been prepared, installation can proceed as described in this chapter.
Table 3-1 Contents in Chapter 3
SectionDescriptionPage Number
3-1
3-2
3-3
3-4
3-5
3-6
3-7
3-8
3-9
Overview
Installation Reminders
Receiving and Unpacking the Equipment
Preparing for Installation
Completing the Hardware Installation
System Configuration
Connectivity Setup
Storing and Transporting the Unit
Completing the Installation Paperwork
3-1
3-2
3-4
3-13
3-23
3-36
3-52
3-70
3-78
Chapter 3 - Installation 3-1
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Section 3-2
Installation Reminders
3-2-1Average Installation Time
Once the site has been prepared, the average installation time required is shown in Ta bl e 3 -2 below.
Table 3-2 Average Installation Time
Average
Description
Unpacking the scanner0.5 hour
Installing the scanner0.5 hourTime may vary, according to the required configuration
DICOM Option
(connectivity)
3-2-2Installation Warnings
1.) Since the Vivid™ 4 weighs 170 kg (375 lbs) or more, without options, two persons are always
required to unpack it. This is also applicable when installing any additional items in excess of 16 kg
(35 lbs).
2.) 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.
Installation Time
0.5 - 2.0 hoursTime may vary, according to the required configuration
Comments
3-2-2-1System Acclimation Time
Following transport, the Vivid™ 4 system may be very cold, or hot. Allow time for the system to acclimate
o
C increment, when the temperature of
CAUTION
before being switched ON. Acclimation requires 1 hour for each 2.5
the system is below 10
o
C or above 35oC.
Turning the system ON after arrival at the site - without allowing time for acclimation - may
cause system damage!
IRECTION 2392751-100, REVISION 3VIVID™ 4 SERVICE MANUAL
3-2-3Safety Reminders
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 UNIT!
WARNING: Two people are required to unpack the unit, as it is heavy. Two people are also
required whenever a part weighing 19kg (35 lb.) or more must be lifted.
CAUTION: If the unit is very cold or hot, do NOT turn ON power to the unit until it has had
sufficient time to acclimate to its operating environment.
CAUTION: To prevent electrical shock, connect the unit to a properly grounded power outlet.
Do NOT use a three-prong to two-prong adapter, as this defeats safety grounding.
CAUTION: Do NOT wear the ESD wrist strap when you work on live circuits where more than
30 V peak is present.
CAUTION: Do NOT operate the unit unless all board covers and frame panels are securely in
place, to ensure optimal system performance and cooling.
When covers are removed, EMI may be present.
WARNING: ACOUSTIC OUTPUT HAZARD
Although the ultrasound energy transmitted from the Vivid™ 4 ultrasound unit is within
AIUM/NEMA standards and FDA limitations, avoid unnecessary exposure. Ultrasound energy
can produce heat and mechanical damage.
Note:The Vivid™ 4 User Manual should be fully read and understood before operating the unit. Keep
the manual near the unit for reference.
Chapter 3 - Installation 3-3
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Section 3-3
Receiving and Unpacking the Equipment
CAUTION: Please read this section fully before unpacking the Vivid™ 4 ultrasound unit.
Note:The Vivid™ 4 ultrasound unit is shipped from the factory either in a wooden shipping crate, or
in a cardboard shipping carton. Separate instructions are provided for opening and unpacking
each type of container, as follows:
•Unpacking the Wooden Shipping Crate - see section 3-3-1 below.
•Unpacking the Cardboard Shipping Carton - see section 3-3-2 on page 3-9.
3-3-1Unpacking the Wooden Shipping Crate
The Vivid™ 4 ultrasound unit is packed in a wooden crate that has four walls (left, right, front and rear),
the crate base, and the top cover. Each section has rebated joints that are joined together with
Clip-lok
TM
clips.
Figure 3-1 Vivid™ 4 - Wooden Shipping Crate
3-3-1-1Removing the Clip-lok
TM
Clips
When unpacking the Vivid™ 4 ultrasound unit, always remove the Clip-lok
1) Locate and remove the clip remover tool (item 23) that is secured on the outside of the wooden
crate, as shown in Figure 3-1, above.
2) Insert the hand level of the clip remover tool under the flange of the long leg of the clip.
3) Place your free hand over the clip to prevent injury when the clip is removed.
4) Rock the lever downwards towards the edge of the case, to remove the clip.
3-4Section 3-3 - Receiving and Unpacking the Equipment
TM
clips as follows:
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3-3-1-2Unpacking and Removing the Unit from the Wooden Crate
Before unpacking the unit, inspect the wooden crate for damage. Inspect the Drop and Tilt indicators
(on the Shock-watch and Tilt-watch labels, respectively) for evidence of accidental shock or tilting of the
crate during transit - see Figure 3-2 below).
NOTE:If the crate is damaged, or if either the Drop or Tilt indicators have turned red (showing failure),
please inform the GE Medical Systems sales representative immediately. In addition, mark on
the shipping consignment note or packing slip/post-delivery checklist (in the “Package” column)
that the Tilt and/or Drop indicators show failure.
Drop indicators turn Red
Tilt indicators turn Red
Figure 3-2 Drop and Tilt Indicators
It is recommended to keep and store the crate and all other packing materials (including the Clip-lok
TM
clips, support foams, anti-static plastic cover, etc.), in the event that transport or shipment of the unit to
a different location will be required in the future.
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CAUTION: When using sharp tools to open packing materials, take care to avoid cutting or damaging
the contents.
Note:Unless otherwise specified, referenced items are shown in Figure 3-1 on page 3-4.
1) Cut and remove the three securing steel strips (item 16).
2) Release the eight Clip-lok
TM
clips (item 15) securing the front wall (item 13) and remove the front
wall. (Refer to the procedure described in Section 3-3-1-1 on page 3-4).
3) Release the eight Clip-lok
TM
clips securing the back wall (item 14) and remove the back wall.
4) Remove the small cartons containing the probes and peripheral options (items D and E in Figure 3-3
below) from the wooden crate.
Figure 3-3 Probes and Peripherals in Original Packaging
5) Remove the console control support back foam (item 11 in Figure 3-3, above).
6) Remove the keyboard support foam located in front of the keyboard (item 10 in Figure 3-3, above).
7) Remove the back support foam located in front of the rear wheels (item 9 in Figure 3-3, above).
8) Remove the top cover by opening the six clips fastening it to the right and left walls. For details on
opening the clips, refer to Section 3-3-1-1 on page 3-4.
9) Remove the right wall (item 6) and the left wall (item 7) by opening the three clips fastening each to
the base.
10) Cut and remove the antistatic sheet (item 2 in Figure 3-4 below) that is wrapped around the unit,
taking care not to damage the antistatic cover.
11) Remove the antistatic cover (item 4 in Figure 3-4).
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12) Remove the two monitor foam supports (item 12 in Figure 3-4), located one on each side of the monitor.
Figure 3-4 Antistatic Cover, Supports and Accessories
13) Remove the three silica gel (moisture absorbing) bags (item 5 in Figure 3-4, above) located under
the unit.
14) Raise the control console (monitor) by pressing the release grip located under the unit’s front handle.
15) Remove the two cartons containing the external cables and accessories located under the control
console, and then lower the control console.
16) Lay the top cover (removed from the crate in step 8 on page 3-6) on the floor and push it over the
narrow side of the base, in front of the unit, to act as a ramp (item 3 in Figure 3-5 below).
Figure 3-5 Removing the Unit from the Wooden Crate
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17) Press the brake pedal, located near the bottom of the front of the unit, to the right, to prevent the
wheels from swiveling, as described in the Swivel Brake Label section, page 1-23.
18) Pull the unit backwards from the platform base onto the ramp and roll it down to the floor.
19) Press the brake pedal, located near the bottom of the front of the unit, to the left, to lock the wheels,
as described in the Parking Label section, page 1-23.
20) Verify the contents of the case, as described in Verifying the Shipping Crate Contents on page 3-13.
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3-3-2Unpacking the Cardboard Shipping Carton
The Vivid™ 4 ultrasound unit is packed in a cardboard shipping carton comprising a durable outer
cardboard carton cover, and a wooden platform base; these are firmly joined together with clamps and
screws. A ramp for rolling the Vivid™ 4 ultrasound unit off the platform, is also included.
Figure 3-6 Vivid™ 4 - Cardboard Shipping Carton
3-3-3Unpacking and Removing the Unit from the Cardboard Shipping Carton
Before unpacking the unit, inspect the carton case for damage. Inspect the Drop and Tilt indicators (on
the Shock-watch and Tilt-watch labels, respectively) for evidence of accidental shock or tilting of the
crate during transit - refer to Figure 3-2 on page 3-5.
NOTE:If the crate is damaged, or if either the Drop or Tilt indicators have turned red (showing failure),
please inform the GE Medical Systems sales representative immediately. In addition, mark on
the shipping consignment note or packing slip/post-delivery checklist (in the “Package” column)
that the Tilt and/or Drop indicators show failure.
It is recommended to keep and store the cardboard shipping carton and all other packing materials
(including the support foams, anti-static plastic cover, etc., in the event that transport or shipment of the
unit to a different location will be required in the future.
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CAUTION: When using sharp tools to open packing materials, take care to avoid cutting or damaging
the contents.
Note:Unless otherwise specified, referenced items are shown in Figure 3-6 on page 3-9.
1) Cut and remove the three securing steel strips (item 13).
2) Cut the adhesive tape along the center of the top of the cardboard shipping carton (item 14).
3) Remove all the fastening staples (item 15) and remove the two screws (item 16) so that the
cardboard carton (item 12) is free of the wooden platform (item 4), and the narrow flap is free.
4) Open the narrow side flap of the carton, remove the ramp (item 5) and attach it to the narrow side
of the wooden platform (item 4 in Figure 3-7 below).
Figure 3-7 Platform View of Shipping Carton
5) Remove the small boxes containing the accessories, probes and peripherals from the shipping carton.
6) Clear away the carton cover (item 12) from the wooden platform on which the ultrasound unit is
standing.
7) Cut and remove the antistatic sheet (item 6 in Figure 3-7, above) that is wrapped around the
ultrasound unit, taking care not to damage the antistatic cover (item 11 in Figure 3-8 below)
covering the unit. Remove the antistatic cover.
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Figure 3-8 Front and Side View of the Unit in the Shipping Carton
8) Pull out and remove the monitor support (item 10 in Figure 3-9 below) from under the base of the
monitor.
Figure 3-9 Unit in Shipping Carton - Right View
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9) Release the front stopper (item C in Figure 3-10 below) by sliding the metal sleeve located at the
locking pin’s base upwards, and then turning it towards you.
Figure 3-10 Front Stopper Location
10) Remove the three silica gel (moisture absorbing) bags (item 7 in Figure 3-10, above) located
underneath the ultrasound unit.
11) Raise the control console (monitor) by pressing the release grip located under the unit’s front handle
and remove the two cartons (item 8 in Figure 3-8 on page 3-11) from underneath the control
console. These cartons contain the external cables and accessories.
12) Lower the control console to its lowest position.
13) Remove the manuals (item 4 in Figure 3-8 on page 3-11) from the compartment on the left side of
the ultrasound unit.
14) Press the brake pedal, located near the bottom of the front of the unit, to the right, to prevent the
wheels from swiveling, as described in the Swivel Brake Label section, page 1-23.
15) Carefully pull the unit backwards from the platform base onto the ramp and roll it down to the floor.
16) Press the brake pedal, located near the bottom of the front of the unit, to the left, to lock the wheels,
as described in the Parking Label section, page 1-23.
17) Verify the contents of the shipping carton, as described in Verifying the Shipping Crate Contents on
page 3 - 13.
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Section 3-4
Preparing for Installation
3-4-1Confirming Customer Order
When preparing for installation of a Vivid™ 4 system, it is important to verify that all items ordered by
the customer have been received. Compare all items listed on the packing slip (shipping consignment
note) with those received and report any items that are missing, back-ordered, or damaged, to your GE
Medical Systems sales representative.
3-4-2Verifying the Shipping Crate Contents
The following sections list the contents of the shipping crate (or shipping carton). Ensure that all
components are present before completing the installation.
3-4-2-1External Cables
The ECG cable (item number 10 or 11) is supplied according to installation location.
IRECTION 2392751-100, REVISION 3VIVID™ 4 SERVICE MANUAL
3-4-2-2Accessories
Table 3-5 Vivid™ 4 Accessories
Item
NumberP/NDescriptionQuantity
12390932
22277423
3066E0007
4E11821AE
52277190
3-4-3Component Inspection
After verifying that all the required parts are included in the shipping crate, inspect the system
components using the checklist supplied below. In addition, ensure that all the labels described in
Chapter 1 - Introduction are present, accurate and in good condition, and enter the serial number printed
on the main label into the system installation details card, as described in System Installation Details on
page 3-78.
3-4-3-1Damage Inspection Checklist
Visually inspect the contents of the shipping crate/shipping carton for damage. If any parts are damaged
or missing, contact an authorized GE Service Representative.
A Damage Inspection Checklist is provided in Table 3-6 on page 3-15.
CD WITH SW V4.2 VIVID4 SYSTEM
DISKETTE 3.5” 1.44MB
FOOTSWITCH
ULTRASOUND GEL BOTTLE
MO DISKETTE 2.3GB (OPTIONAL)
1
1
1
1
1
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Table 3-6 Damage Inspection Checklist
b
StepItemRecommended Procedure
1
Console
2
Probe HoldersClean the gel wells with warm water and a damp cloth to remove all traces of gel.
3
Control Panel
4
Probes
5
Monitor
6
Fans
7
BE Rear Panel
8
Covers
9
Peripherals
Verify that the system is switched OFF and unplugged. Clean the console and
control panel.
Physically inspect the control panel for missing or damaged items. Verify the proper
illumination of all the control panel buttons.
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 unit. Verify
that the EMI fingers around the probe connector socket housing are intact. Check
the probe locking mechanism and probe switch.
Clean the CRT with a soft cloth dampened with water. Repeat using only water,
and wipe with a dry cloth. Inspect the monitor for scratches and raster burn.
Verify that the FE crate cooling fans, BE fan and peripheral fans are operating and
clean.
Check the BE 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.
Check that all screws are in place, all chassis and internal covers are installed and
that the air filters are in place.
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
AC System
11
Power Cord
12
Front Castors
13
Rear CastorsCheck that the rear castors can roll and swivel but cannot lock.
Check the AC board connectors and the associated cabling for good connection
and proper insulation. Verify that the connections are secured.
Check the power cord for cuts, loose hardware, tire marks, exposed insulation, or
any deterioration. Verify continuity. Tighten the clamps that secure the power cord
to the unit and the outlet plug to the cord. Replace the power cord and/or clamp, as
required.
Check that the front castors can swivel, and can be placed in swivel lock and full
lock by the foot brake pedal.
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3-4-3-2Front and Side View of the Vivid™ 4 Ultrasound Unit
Figure 3-11 below shows the Vivid™ 4 ultrasound unit components that are visible from the front and
side of the ultrasound unit.
1
11
12
13
14
15
2
3
4
5
6
16
7
17
8
18
9
19
LEFT
Note: (10) Footswitch not illustrated
RIGHT
Figure 3-11 Front and Side View of the Vivid™ 4
1Display Monitor: Swivels to the left and right, and tilts up and down.
2Speakers: Two loudspeakers for Doppler sound.
3Probe Holders and Probes: Situated on either side of the front panel.
4Control Panel: Contains the alphanumeric keyboard and the buttons used to operate the ultrasound
unit.
5Front Handle.
6Raise/Lower the Control Console Up/Down/Swivel Handle: Located midway underneath the front
handle. Used to swivel (left or right) and raise or lower the control console (control panel and
monitor). Press the handle halfway for the swivel action, and all the way for the raising/lowering
action.
7Air Filter: Located above the crate.
8Probe Ports:
•Four active probe connectors (one for a pencil probe).
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9Foot Brake: Three-position brake, as follows:
•LEFT (P) locks the wheels.
•MIDDLE unlocks the wheels.
•RIGHT (double arrows) locks the swivel action.
10 (Not shown in Figure 3-11)
Footswitch: Configurable footswitch connected to the patient I/O module that enables keyboard
commands to be operated by foot.
11 Gel Holders: Situated on either side of the control console, and on the top surface on either side of
the monitor.
12 Color Printer or optional storage area.
13 On/Off Switch.
14 Alphanumeric Keyboard and Operation Buttons.
15 Cable Hook.
16 Peripherals: The VCR recorder and/or black-and-white printer and/or color printer are positioned on
the peripheral storage area of the control console.
17 CD Read/Write (CDRW) and MO Disk (optional).
18 Rear Castors.
19 Front Castors.
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3-4-3-3Rear View of the Vivid™ 4 Ultrasound Unit
The following figure shows the Vivid™ 4 ultrasound unit components that are visible from the rear of the
ultrasound unit:
1
2
2
3
5
9
Figure 3-12 Rear View of the Vivid™ 4
1Monitor
2Gel Wells
3Monitor Connection Panel
4Left Rear Panel
4
6
7
8
5Right Rear Panel
6Power Cable Storage Hook
7Circuit Breaker On/Off Switch
8Ground Screw
9Power Cable Socket
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3-4-4System Voltage Confirmation
3-4-4-1System Voltage Settings
Verify that the scanner is set to the correct voltage.
The Voltage settings for the Vivid™ 4 Scanner are found on a label to the right of the Power switch and
External I/O, on the rear of the system.
Figure 3-13 Rating Plate Example
WARNING: CONNECTING A Vivid™ 4 SCANNER TO THE WRONG VOLTAGE LEVEL WILL MOST
LIKELY DESTROY THE SCANNER.
3-4-4-2Confirming System Voltage Configuration
1) Turn ON the system.
2) In regular 2D Scanning Mode, press Config.
3) From the System Configuration dialog box, click the Technical Support tab.
4.) Make sure the frequency and voltage ranges are set up correctly and that the appropriate settings
are displayed in the Power Supply Frequency and Nominal Voltage fields (lower right side of the
dialog box) - see Figure 3-14 on page 3-20.
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Figure 3-14 System Configuration Technical Support Tab
5) Click OK.
Note:If the voltage is not set correctly, contact an authorized GE Service Representative.
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3-4-5Video Formats Confirmation
The Vivid™ 4 ultrasound scanner and VIC may be configured to operate with either PAL or NTSC video
systems, as required.
3-4-5-1Video Format Confirmation
1) Turn ON the system and the check video transmission signal is set correctly.
2) Press Config.
3) From the System Configuration dialog box, select the VCR/ECG tab and make sure Either PAL or
NTSC is selected.
4) Click the Technical Support tab and make sure Frequency is set to either 60Hz for NTSC, or 50Hz
for PAL.
5) Click OK.
Note:If the video format is not set correctly, contact an authorized GE Service Representative.
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3-4-6Ensuring Protection from EMI
The Vivid™ 4 unit 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 unit 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 in the following table are followed:
Note:The Vivid™ 4
qualified facilities, in terms of the prevention of radio wave interference. Operation of the
ultrasound unit
television sets situated near the medical equipment.
Table 3-7 EMI Prevention/ Abatement
EMI RuleDetails
Ground the unit.
Be aware of RF sources.
Replace and/or reassemble
all screws, RF gaskets,
covers and cores.
Replace broken RF gaskets.
Do not place labels where
RF gaskets touch metal.
ultrasound unit is approved for use in hospitals, clinics and other environmentally
in an inappropriate environment can cause electronic interference to radios and
Poor grounding is the most likely reason an ultrasound unit will have noisy images. Check
the grounding of the power cord and power outlet.
Keep the unit at least 5m (16.4 ft) away from other EMI sources. Special shielding may be
required to eliminate interference problems caused by high frequency, high powered radio
or video broadcast signals.
After you finish repairing or updating the system, replace all covers and tighten all screws.
Any cable with an external connection requires a magnet wrap at each end. Install the shield
over the front of the card cage. Loose or missing covers or RF gaskets allow radio
frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket.
Do not turn on the unit until any loose metallic part is removed and replaced if needed.
Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit
RF leakage. In case a label has been found in such a location, move the label to a different
appropriate location.
Use GE specified harnesses
and peripherals.
Take care with cellular
phones.
Properly address peripheral
cables.
The interconnect cables are grounded and require ferrite beads and other shielding. Cable
length, material, and routing are all important; do not make any changes that do not meet
all specifications.
Cellular phones may transmit a 5 V/m signal that causes image artifacts.
Do not allow cables to lie across the top of the card cage or hang out of the peripheral bays.
Loop any peripheral cable excess length inside the peripheral bays or hang on the hooks
provided below the console. Attach the monitor cables to the frame.
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Section 3-5
Completing the Hardware Installation
It is recommended to pay attention to the system specifications and make sure the facility has been
prepared in accordance with the information provided in Chapter 2 - Pre-Installation.
For easy reference, the physical specifications of the Vivid™ 4 ultrasound unit are shown in Table 3-8
below.
Table 3-8 Vivid™ 4 - Physical Specifications
Metric
Measurement
Height (with monitor)131 — 145 cm51.6 — 57.1 in
Width62.5 cm25 in
Depth
Weight170 kg375 lbs
Specifications
112 cm
(100 cm without rear handle)
Imperial
Specifications
44 in
(40 in without rear handle)
When moving the system, always adhere to the following the precautions:
CAUTION: At least two people must be available to deliver and unpack the Vivid™ 4 ultrasound
unit. Attempts to move the unit considerable distances (or on an incline) by one person alone,
could result in personal injury, and/or damage to the system.
CAUTION: The Vivid™ 4 weighs 170 kg (375 lbs) or more - depending on installed peripherals when ready for use. Care must be used when moving it or replacing its parts. Failure to follow
the precautions listed could result in injury, uncontrolled motion and costly damage.
ALWAYS:
Be sure the pathway is clear.
Use slow, careful motions.
Use two people when moving the system on inclines or lifting more than 16 kg (35 lbs).
3-5-1Connecting the Footswitch
1) Connect the triple footswitch to the Footswitch input on the left side of the front panel, as shown in
Figure 3-8 on page 3-11.
2) After connecting the peripherals and switching the system on, configure the footswitch, as
described in System Tab on page 3-37.
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3-5-2Connecting Peripherals
Peripheral devices, such as a VCR or printer, are connected to the Vivid™ 4 ultrasound unit using the
rear panel connectors. Ensure that all peripheral devices connected to the ultrasound unit comply with
national safety requirements for medical equipment, including IEC601, CSA22.2, AS3200.1 and UL544.
The Vivid™ 4 ultrasound unit can operate with one or more of the following types of on-board
peripherals:
•VCR
•Black & White (B/W) Printer
•Color Printer (may be installed in side compartment)
•HP Deskjet 6122 Color Printer
Note:Each of the peripherals have European and US versions. For a complete list of recommended
peripherals, refer to the Vivid™ 4 User Manual. For information for each peripheral device, refer
to the manufacturer’s manual.
On-board peripherals must be connected to one of the two available auxiliary power supplies on the
right rear panel. The total load on both auxiliary AC outlets should not exceed 500 VA. This means
8 Amp @ 100-120V AC or 4 Amp @ 220-240V AC.
Voltages are set according to local country voltage, as described in the Voltage Level Checks section,
on page 3-32.
For more details about peripherals installation, refer to Chapter 8 - Replacement Procedures - see the
Peripherals section, on page -114.
3-5-2-1Rear Panel Connectors
The Vivid™ 4 ultrasound unit is equipped with two rear panels that provide the connections for
peripheral devices, as shown in Figure 3-15 below.
Note:Right and left are determined from the front of the unit. Refer to the Right Rear Panel Connectors
section, on page 3-25, and to the Left Rear Panel Connectors section, on page 3-26, for details
about each panel.
Right Rear Panel
Left Rear Panel
Figure 3-15 Rear Panel Connectors Rear View
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3-5-2-1-1Right Rear Panel Connectors
Table 3-9 describes the connectors included in the right rear panel (shown in Figure 3-16):
1
2
3
4
5
Figure 3-16 Right Rear Panel Connectors
Table 3-9 Right Rear Panel Connectors
NameDescription
1. AUXILIARY AC OUTLET
For use with external peripherals. Voltages are set according to local country
voltage.
3
6
7
8
For use with external peripherals. Voltages are set according to local country
5. MODEMFor use with the service platform (iLinq).
6. RS 232 (2)Not in use.
7. USBFor GE Service usage only (not for external USB devices).
8. PARALLEL PORT25 pin connector for use with the external peripherals.
voltage. If additional auxiliary outlets are required, use the special cable
provided by GE. DO NOT attempt to connect additional peripherals using an
external wall outlet.
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3-5-2-1-2Left Rear Panel Connectors
Table 3-10 describes the connectors included in the left rear panel (shown in Figure 3-17):
1
2
4
7
8
9
10
Figure 3-17 Left Rear Panel Connectors
Table 3-10 Left Rear Panel Connectors
NameDescription
3
5
6
11
12
1.VCR-RS 232 (1)One standard 9-pin RS232 (1) connector for VCR control (COM 1).
2.S-VIDEO OUT Y/C Video Out: 4 pin connector for output to an S-VHS VCR.
3.S-VIDEO INY/C Video In: 4 pin connector for input from an S-VHS VCR.
4.VIDEO OUT B/WBNC connector for composite B/W video output to a hard copy printer.
5.VIDEO OUT 1BNC connector for composite color video output (PAL or NTSC).
6.VIDEO OUT 2BNC connector for composite color video output (PAL or NTSC).
7.AUDIO IN (RIGHT)RCA jack.
8.AUDIO IN (LEFT)RCA jack.
9.AUDIO OUT (RIGHT)RCA jack.
10.AUDIO OUT (LEFT)RCA jack.
11.MICMicrophone input.
12.PRINT TRIG.
BNC connector for the exposure control of a multi-imager or another peripheral
activated by pressing Print B.
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3-5-2-2Connecting the VCR
1) Place the VCR on the peripheral tray and connect the following:
Table 3-11 VCR Cables
From the VCRTo the Left PanelDIP on VCR Right Panel
S-Video INS-Video OUT (Y/C OUT) 1-4 OFF (down)
S-Video OUTS-Video IN (Y/C OUT)5-6 ON (up)
Audio INAudio OUT
Audio OUTAudio IN
BE Control (RS-232)VCR RS 232 (1)
2) Install the VCR according to the VCR installation schematics, see Figure 8-119 on page 8-126.
3) After connecting the remaining peripherals and switching the system on, configure the VCR
settings, as described in the VCR/ECG Tab section, on page 3-45.
For more details about peripherals installation refer to Chapter 8 - Replacement Procedures - see the
Peripherals section, on page -114.
3-5-2-3Connecting the Black & White Printer
1) Place the printer on the peripheral tray and connect the following cables as shown in Table 3-12.
Table 3-12 Black & White Printer Cables
From the PrinterTo the Left Panel
Video INComposite Video OUT B/W
External TriggerPrint Trigger
Power CableRight Connectors Panel AC outlet
2) Install the printer according to the printer’s installation schematics, see Figure 8-101 on page -115.
3) After connecting the remaining peripherals and switching the system on, configure the printer
settings, as described in the Printers Tab section, on page 3-44.
For more details about peripherals installation refer to Chapter 8 - Replacement Procedures - see the
Peripherals section, on page -114.
3-5-2-4Connecting the Color Printer
1) Place the color printer in the printer compartment above the B/W printer and VCR on the peripheral
tray, using an additional shelf (or place the color printer in the side compartment).
2) Connect the following cables as shown in Ta bl e 3- 13 :
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Table 3-13 Color Printer Cables
To the Cables
From the Color Printer
Video INR, G, B, Sync
External TriggerPrint Trigger
AC INAC Power Cable
underneath the Control Console
Note:All the color printer cables are located in the left storage compartment under the metal cover.
3) After connecting the remaining peripherals and switching the system ON, configure the printer
settings, as described in the Printers Tab section, on page 3-44.
For more details about peripherals installation, refer to Chapter 8 - Replacement Procedures - see the
Peripherals section, on page -114.
3-5-2-5Connecting the HP DeskJet 6122 Color Printer
Note: If there is sufficient space, the HP DeskJet 6122 Color Printer may be installed under the
control console. Alternatively, it will require a suitable stand or table to be positioned in
close proximity to the Vivid™ 4 scanner - at a distance of not more than 1m (3.3 ft) from the
power connection to the Vivid™ 4 unit.
WARNING: Whenever moving the Vivid™ 4 scanner, the DeskJet Color Printer must be
disconnected from the scanner. DO NOT attempt to move the two units simultaneously without
first disconnecting them. After relocation, re-connect the printer to the scanner.
1) Place the DeskJet color printer on the shelf below the control console (or alternatively on the
designated stand or table, adjacent to the unit).
2) Connect the following cables as shown in Ta ble 3 -1 4:
Table 3-14 DeskJet Color Printer Cables
From the Color PrinterTo the Right Panel
Parallel Port ConnectorParallel Port
AC IN (AC Dual Power cable)Panel AC outlet
3) After connecting the remaining peripherals and switching the system ON, configure the printer
settings, as described in the Printers Tab section, on page 3-44.
For more details about peripherals installation refer to Chapter 8 - Replacement Procedures - see the
Peripherals section, on page -114.
3-28Section 3-5 - Completing the Hardware Installation
Page 100
GE MEDICAL SYSTEMS
D
IRECTION 2392751-100, REVISION 3VIVID™ 4 SERVICE MANUAL
3-5-3Connecting Probes
The Vivid™ 4 ultrasound unit operates with various types of probes that are used for scanning patients,
including flat phased, convex and linear electronic array probes. Once connected, the probes can be
selected for different applications.
There are four active probe connectors on the unit’s control panel (one connector is for a pencil probe).
Probes can be connected or changed any time, as described below:
1) Inspect the probe socket to verify that it is free of debris.
2) Hold the rectangular probe connector vertically so that the probe’s cable points upwards.
3) Rotate the probe locking latch counterclockwise to the unlock (horizontal) position.
4) Gently insert the connector into one of the matching sockets on the front of the unit. Gently push
the connector in as far as possible.
5) Rotate the locking latch 90 degrees clockwise to lock the connector into place (vertical).
NOTE:It is not necessary to turn OFF power to connect or disconnect a probe.
3-5-3-1Available Probes
The following probes are available for use with the Vivid™ 4 ultrasound unit:
Table 3-15 Available Probes
P/NDescription
2256686Heart Sound Microphone
2259153Probe: C358 (outside Japan)
E8386RKBiopsy Kit for C358
2301959Probe: C721 (Curved)
2259206Probe: I739L Linear
2323337Probe: 3S Sector
2263669Probe: 7S Sector
2290751Probe: 5S Sector
2294523Probe: 10L (739L) Linear
2295377Probe: 39A (12L) Linear
E83885MMBiopsy Kit for 10L/12L
2298589Probe: 10S
2259258Probe: P509 (Japan)
2259246Probe: T739L Linear
2294521Probe: 7L (546L)
KN100068Probe: 6T (Super TEE)
KN100023Probe: 8T (PED TEE)
KN100072Probe: 9T(PED TEE) (for RFI systems only)
KZ200476Probe: Adaptor PAMPTE/6Tv
TY200774Probe: Wall Rack TEE
TE100024Probe: Pencil P2D
TQ100002Probe: Pencil P6D
2301954Probe: E721 OB/GYN
KQ100006Probe: i8L Linear
KW100011Probe: i13L Linear
Chapter 3 - Installation 3-29
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