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GE Vivid 7 Service Manual

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    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    Chapter 1 - Introduction 1 - 63
    1-5-29      Labe l, Disassembly Nester, Part 1 (L eft Part of Label) (cont’d)
    (Label introduced September 2005.)
    Figure 1-19   Label, Disassembly Nester, Part 1 (Left Part of Label) 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    1 - 64 Section 1-5 - Labels Locations
    1-5-29      Labe l, Disassembly Nester, Part 1 (L eft Part of Label) (cont’d)
    (Label used before September 2005.)
     
    Figure 1-20   Label, Disassembly Instru ction, Part 1 (Left Part of Label)
    DISASSEMBLY INSTRUCTIONS
    Remove all screws on rear side of monitor cover, and remove cover. 
    Remove all screws on rear side of monitor front cover, and remove front cover.
    Remove all screws on the cover located under the shelf underneath the monitor, and remove cover. 
    Detach monitor by removing four unbrako screws located underneath the monitor neck.
    Remove shelf by loosening all screws underneath it and remove speakers from shelf. 
    Remove all screws underneath operators panel. Disconnect and remove alphanumeric keyboard and
    operators panel.
    Remove probe holders and front handle.
    Remove all unbrako screws, which fasten the top console c able to the console and loosen the cable.
    Remove top console and horizontal movement mechanism by unscrewing the big unbrako screw on
    top of the rear base of the horizontal movement mechanism.
    Remove all quarterturn screws on both sidepanels of the system. Side panels can now be removed. 
    Remove screws underneath the pedals to remove the pedal plastics. 
    Remove the footrest bumper by unscrewing four screws.
    Remove all screws on the rear-, top- and front covers to loosen the covers.
    Remove rear handle by unscrewing all screws.
    Remove fan cover by removing all fastening screws.
    Remove fan bracket w/fan by removing all fastening screws.
    Remove all peripheral units.
    Disconnect, then remove all cables.
    Detach computer by unscrewing all fastening screws.
    Remove external i/o box by unscrewing all fastening screws.
    Remove internal i/o box by unscrewing all fastening screws.
    Remove ac-power box by unscrewing all fastening screws.
    Remove ac-transformer box by unscrewing all fastening screws.
    Remove sheet metal cover on electronic rack on lower right side.
    Remove all PCB’s from the electronic rack. 
    Remove the two power supplys from the electronic rack by unscrewing all fastening screws.
    Unscrew two screws on the connector (front) panel of the electronic rack, and remove the panel.
    Remove the electronic cabinet by unscrewing all fa stening screws in front of it and behind of it. 
    Remove the pedal mechanism by unscrewing all fastening screws.
    Remove the wheels by unscrewing all fastening screws. 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    Chapter 1 - Introduction 1 - 65
    1-5-30 Label, Disassembly Nester,  Part 2 (Right Part of Label)
    Located on the outside of the Front-End Card Rack’s Cover (inside unit)
    (Label introduced October 1, 2007)
    Figure 1-21   Label, Di sassembly Instruction, Part 2 (Right Part of Label)
    Special items/material Location information
    1 Lithium  BEP battery
    2  Lead  BEP standby battery (option)
    3  Printed circuit boards  Circuit boards inside all sub units
    4  LCD  Main LCD on the system
    5  External electric cables  Part of the trolley
    6  Electrolyte capacitors  Inside BEP-, AC-, DC- and TX power
    7  Nitrogen filled gass spring  User Interface locking system
    8  Cathode ray tubes  Main CRT on the system
    BEP
    CRT
    LCD
    1
    7
    8
    3
    3
    3
    3
    2
    3
    6
    FB314971-04
    Card
    Rack3
    3
    5
    6
    4
    33
    All models 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    1 - 66 Section 1-5 - Labels Locations
    1-5-30      Labe l, Disassembly Nester, Part 2 (R ight Part of Label) (cont’d)
    (Label introduced September 2005)
    Figure 1-22   Label, Di sassembly Instruction, Part 2 (Right Part of Label) 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    Chapter 1 - Introduction 1 - 67
    1-5-30      Labe l, Disassembly Nester, Part 2 (R ight Part of Label) (cont’d)
    (Label used before 2005)
     
    Figure 1-23   Label, Disassembly Instru ction, Part 2 (Right Part of Label)
    PARTS DESCRIPTION DISPOSITION
    Painted sheet metal, aluzinc steel Recyclable metal after cleaning
    Sheet metal, aluzinc Recyclable metal
    Printed circuit boards Recycling
    Cables Recyclable metal. All cables are UL 
    listed.
    Nuts, steel + nylock Recyclable metal after cleaning 
    Nuts, steel  Recyclable metal 
    Screws, steel + painted Recy clable metal after cleaning
    Screws, steel  Recyclable metal 
    Casters w/rubber Recyclable metal and plastics
    Beryllium copper Recyclable metal
    Lithium battery To be handled by battery recycler
    Covers, made from ABS plastic To be handled by plastics recycler
    Bumpers, made from EPP 
    (expanding polypropylen)To be handled by plastics recycler
    Shelf made from Polyuretan, liquid
    painted
    To be handled by plastics recycler
    Foot pedal, plastics made from EPP 
    (expanding polypropylen)To be handled by plastics recycler
    Peripheral units Follow disassembly/recycling instructions
    from original manufacturer
    Computer Follow disassembly/recycling instructionsfrom original manufacturer
    Ferrite cores  Reusable
    Electric fans  Reusable 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    1 - 68 Section 1-6 - Dangerous Procedure Warnings
    Section 1-6
    Dangerous Procedure Warnings
    Warnings, such as the example below, precede po tentially dangerous procedures throughout this 
    manual. Instructions contained in the warnings must be followed.
    DANGERDANGEROUS VOLTAGES, CAPABLE OF  CAUSING DEATH, ARE PRESENT IN 
    THIS EQUIPMENT. USE  EXTREME CAUTION WHEN HANDLING, TESTING AND 
    ADJUSTING.
    WARNINGWARNINGIF THE COVERS ARE REMOVED FROM AN OPERATING Vivid 7, SOME METAL 
    SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF 
    TOUCHED, EVEN WHILE IN SHUT DOWN MODE.
    WARNINGWARNINGEXPLOSION WARNING
    DO NOT OPERATE THE EQUIPMENT IN AN  EXPLOSIVE ATMOSPHERE. OPERATION 
    OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A 
    DEFINITE SAFETY HAZARD.
    WARNINGWARNINGDO 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. 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    Chapter 1 - Introduction 1 - 69
    Section 1-7
    Lockout/Tagout (LOTO) Requirements
    Follow OSHA Lockout/Tagout requirements (USA)  or local Lockout/Tagout requirements by ensuring 
    you are in total control of the AC power  plug at all times during the service process.
    To apply Lockout/Tagout:
    1.) Plan and prepare for shutdown.
    2.) Shutdown the equipment.
    3.) Isolate the equipment.
    4.) Apply Lockout/Tagout Devices.
    5.) Control all stored and residual energy.
    6.) Verify isolation.
    All potentially hazardous stored or residual energy is relieved.
    Section 1-8
    Returning/Shipping Prob es and Repair Parts
    Equipment being returned must be clean and free of blood and other infectious substances.
    GEHC policy states that body fluids must be proper ly removed from any part or equipment prior to 
    shipment. GEHC employees, as well as customers,  are responsible for ensuring that parts/equipment 
    have been properly decontaminated prior to ship ment. Under no circumstance should a part or 
    equipment with visible body fluids be taken or shipped  from a clinic or site (for example, body coils or 
    an ultrasound probe). The purpose of the regulati on is to protect employees in the transportation 
    industry, as well as the people who  will receive or open this package.
    NOTE: The US Department of Transportation (DOT) ha s ruled that “items that were saturated and/or 
    dripping with human blood that are now caked with dried blood; or which were used or intended 
    for use in patient care” are “regulated medical wa ste” for transportation purposes and must be 
    transported as a hazardous material.
    NOTICEEnergy Control and Power Lockout for Vivid 7.
    When servicing parts of the system where there  is exposure to voltage greater than 30 Volts:
    1.) Turn off the breaker.
    2.) Unplug the system.
    3.) Maintain control of the system power plug.
    4.) Wait for at least 20 seconds for c apacitors to discharge as there are no  test points to verify isolation. 
    Beware that the AC Control Box,  Front End Processor and Back End Processor may be energized even 
    if the power is turned off  when the cord is still plugged into the AC Outlet.
    SignedDate
    TA G 
    & LOCKOUT 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    1 - 70 Section 1-9 - Electromagnetic Compatibility (EMC)
    Section 1-9
    Electromagnetic Compatibility (EMC)
    1-9-1 What is EMC?
    Electromagnetic compatibilit y describes a level of performance of  a device within its electromagnetic 
    environment. This environment consists of the de vice itself and its surroundings including other 
    equipment, power sources and pers ons with which the device must interface. Inadequate compatibility 
    results when a susceptible device fails to perform as  intended due interference from its environment or 
    when the device produces unacceptable levels of emi ssion to its environment. 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 of sign al 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.
    1-9-2 Compliance
    Vivid 7 conforms to all applicable conducted and  radiated emission limits and to immunity from 
    electrostatic discharge, radiated an d conducted RF fields, magnetic fields and power line transient 
    requirements.
    Applicable standards are: 47CFR Part 18, IEC60601–1–2:2001. 
    NOTE: For CE Compliance, it is crit ical that all covers, screws, shielding, gaskets, mesh, clamps, are 
    in good condition, installed  tightly without skew or stress. Pr oper installation following all 
    comments noted in this service manual is required in order to achieve full EMC performance.
    1-9-3 Electrostatic Discharge (ESD) Prevention
     
    WARNINGWARNINGDO NOT TOUCH ANY BOARDS WITH INTEGRAT ED CIRCUITS PRIOR TO TAKING THE 
    NECESSARY ESD PRECAUTIONS: 
    ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED ESD 
    CONNECTION POINT LOCATED AT THE REAR  OF THE SCANNER (TO THE RIGHT OF 
    THE POWER CONNECTOR). 
    FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE 
    EQUIPMENT. 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    Chapter 1 - Introduction 1 - 71
    Section 1-10
    Customer Assistance
    1-10-1 Contact Information
    If this equipment does not work as  indicated in this service manual or in the user manual, or if you 
    require additional assistance, please contact the lo cal distributor or appropriate support resource, as 
    listed below.
    Before you call, identify the follo wing information, and acquire image  (Alt+D) to send to the Customer 
    Care team:
    1.) System ID serial number.
    2.) Software version.
    3.) Date and time of occurrence.
    4.) Sequence of events leading to issue.
    5.) Is the issue reproduceable?
    6.) Imaging mode, probe, preset/application.
    7.) Media brand, speed, capacity, type.
    8.) Save secondary image capture, cine loop, 4D multi-volume loop.
    NOTE: Restart the application befo re resuming clinical scanning. 
    Table 1-24    Phone numbers for Customer Assistance
    LOCATIONPHONE NUMBER
    USA
    GE Healthcare
    Ultrasound Service Engineering
    9900 Innovation Drive
    Wauwatosa, WI 53226 Service: On-site
    Service Parts
    Application Support1-800-437-1171
    1-800-558-2040
    1-800-682-5327 or 1-262-524-5698
    Canada 1-800-668-0732
    Latin America Service
    Application Support1-800-321-7937
    1-262-524-5698
    Europe
    GE Ultraschall Deutscland Gmbh & Co. KG
    Beethovenstraße 239
    Postfach 11 05 60, D-42655 Solingen
    GermanyPhone:   +33 (0) 130-831-300 (General Imaging and Cardiac)
     +43 (0) 7682-3800-26 (Voluson-Logiqbook)
    Fax: +49 (0) 2122-8024-31
    Asia (Singapore)
    GE Ultrasound Asia
    Service Department - Ultrasound
    298 Tiong Bahru Road #15-01/06
    Central Placa
    Singapore 168730
    Tel: +65 6291-8528
    Fax: +65 6291-7006
    Japan Support CenterPhone: 81-426-48-2940
    Fax: 81-426-48-2905 
    						
    							
    GE HEALTHCARE
    DIRECTION FC091194, REVISION 11    VIVID 7 SERVICE MANUAL 
    1 - 72 Section 1-10 - Customer Assistance
    1-10-2 System Manufacturer
    Table 1-25    System Manufacturer
    MANUFACTURERPHONE NUMBERFAX NUMBER
    GE Vingmed Ultrasound A/S
    Strandpromenaden 45
    P.O. Box 141
    N-3191 HORTEN
    NORWAY +47 3302 1100 +47 3302 1350 
    						
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