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GE Logiq 9 Service Manual

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    							GE MEDICAL SYSTEMS PROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
    Chapter 10 Periodic Maintenance 10-27
    10-7-9-5 Data Sheet for Transducer Source Leakage Current
    The test passes when all readings measure less than the values shown in Table 10-15 and Table 10-
    16. Record all data on the PM Inspection Certificate.
    . 
    CAUTIONEquipment damage possibility. Never switch the Polarity and the status of Neutral when the unit 
    is powered ON. Be sure to turn the unit power OFF before switching them using the POLARITY 
    switch and/or the NEUTRAL switch. Otherwise, the unit may be damaged
    Table 10-23 Typical Data Sheet For Transducer Source Leakage Current
    Transducer Tested:
     Unit Power
    Tester Power Polarity 
    SwitchTester GROUND or 
    NUETRAL Switch
    Measurement
    ON NORM OPEN
    ON NORM CLOSED
    ON REV OPEN
    ONREVCLOSED
    OFFNORMOPEN
    OFFNORMCLOSED
    OFF REV OPEN
    OFF REV CLOSED 
    						
    							GE MEDICAL SYSTEMSPROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL   
    10-28 Section 10-8 - When Theres Too Much Leakage Current...
    Section 10-8
    When Theres Too Much Leakage Current...
    CHASSIS FAILS
    Check the ground on the power cord and plug for continuity. Ensure the ground is not broken, frayed, 
    or intermittent. Replace any defective part.
    Tighten all grounds. Ensure star washers are under all ground studs.
    Inspect wiring for bad crimps, poor connections, or damage.
    Test the wall outlet; verify it is grounded and is free of other wiring abnormalities. Notify the user or 
    owner to correct any deviations. As a work around, check the other outlets to see if they could be used 
    instead.
    NOTE: No outlet tester can detect the condition where the white neutral wire and the green grounding 
    wire are reversed. If later tests indicate high leakage currents, this should be suspected as a 
    possible cause and the outlet wiring should be visually inspected.
    PROBE FAILS
    Test the probe in another connector to isolate if the fault lies with the probe or the scanner.
    NOTE: Each probe will have some amount of leakage, dependent on its design. Small variations in 
    probe leakage currents are normal from probe to probe. Other variations will result from 
    differences in line voltage and test lead placement. The maximum allowable leakage current for 
    body surface contact probe differs from inter-cavity probe. Be sure to enter the correct probe 
    type in the appropriate space on the check list.
    If excessive leakage current is slot dependent, inspect the system connector for bent pins, poor 
    connections, and ground continuity.
    If the problem remains with the probe, replace the probe.
    PERIPHERAL FAILS
    Tighten all grounds. Ensure star washers are under all ground studs.
    Inspect wiring for bad crimps, poor connections, or damage.
    STILL FAILS
    If all else fails, begin isolation by removing the probes, external peripherals, then the on board ones, 
    one at a time while monitoring the leakage current measurement.
    NEW UNIT
    If the leakage current measurement tests fail on a new unit and if situation can not be corrected, submit 
    a Safety Failure Report to document the system problem. Remove unit from operation.
    ECG FAILS
    Inspect cables for damage or poor connections. 
    						
    							GE MEDICAL SYSTEMS PROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
    Chapter 10 Periodic Maintenance 10-29
    PM INSPECTION CERTIFICATE  
    * Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other
    FUNCTIONAL CHECKS PHYSICAL INSPECTION AND CLEANING 
    COMMENTS: 
    ______________________________________________________________________________
    ______________________________________________________________________________
    ______________________________________________________________________________
    ______________________________________________________________________________
    Customer Name: System ID: Dispatch Number / Date Performed: Warranty/Contract/HBS
    System TypeModel Number: Serial Number: Manufacture Date:
    Probe 1: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 2: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 3: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 4: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 5: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 6: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 7: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 8: Frequency: Scan Format*: Model Number: Serial Number:
    Probe 9: Frequency: Scan Format*: Model Number: Serial Number:
    Functional Check (if applicable)OK? or 
    N/APhysical Inspection and Cleaning 
    (if applicable) Inspect Clean
    B-Mode Function Console
    Doppler Modes Function Monitor
    CF-Mode Function Touch Panel
    M-Mode Function Air Filter
    Applicable Software Options Probe Holders
    Applicable Hardware Options External I/O
    Control Panel Wheels, Brakes & Swivel Locks
    Monitor Cables and Connectors
    Touch PanelGE Approved Peripherals (VCR, CD-RW, MOD, 
    Printers)
    Measurement Accuracy
    GE Approved Peripherals 
    						
    							GE MEDICAL SYSTEMSPROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL   
    10-30 Section 10-8 - When Theres Too Much Leakage Current...
    ELECTRICAL SAFETY
    Final Check. All system covers are in place. System scans with all probes as expected.
    Accepted by: ______________________________________________________________________
    Electrical Test PerformedMax Value 
    AllowedValue 
    Measured OK? Comments
    Outlet (correct ground &wiring config.)
    System Ground Continuity
    Chassis Source Leakage Current - Probe
    Chassis Source Leakage Current - Caster
    Chassis Source Leakage Current - CRT
    Patient Lead Source Leakage
    (Lead to Ground)
    Patient Lead Source Leakage
    (Lead to Lead)
    Patient Lead Source Leakage
    (Isolation)
    Peripheral 1 Leakage Current
    Peripheral 1Ground Continuity
    Peripheral 2 Leakage Current
    Peripheral 2Ground Continuity
    Peripheral 3 Leakage Current
    Peripheral 3Ground Continuity
    PROBES
    Probe Number 
    (from previous page)Max Value 
    AllowedMax Value 
    Measured OK? Comments
    Probe 1:
    Probe 2:
    Probe 3:
    Probe 4:
    Probe 5:
    Probe 6:
    Probe 7:
    Probe 8:
    Probe 9: 
    						
    							GE MEDICAL SYSTEMS PROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
    Index I
    A,B
    AC Power
    Replacement Procedure, 8-89
    Acoustic Noise Output, 3-9
    Acquisition Diagnostics, 7-14
    Archiving Images
    Move, 4-18
    Automatic Troubleshooting, 7-17
    B/M Mode Processor (BMP) Board, 5-17
    B/M-Mode Checks
    Functional Checks, 4-8
    Back End Processor, 5-23
    See BEP, 8-13
    Theory, 5-23
    Backup
    Patient Database, 4-15
    Preset Configurations, 4-15
    Base Load Software
    Check Devices, 3-31,  , 8-76
    Remapping Drive Letters, 3-33,  , 8-78
    Video Adapter Configuration, 3-32,  , 8-77
    Basic Measurements
    Functional Checks, 4-10
    BEP
    Replacement Procedure, 8-13
    BEP Power Off Path, 5-30
    BEP Power On, 5-29
    BEP Power On Path, 5-29
    Block Diagram
    Simple System, 5-3
    BMP Board
    General Description, 5-17
    Receive Signal Processing, 5-18
    BMP Diagnostics
    Board Level, 7-24
    Body pattern
    display location, 4-7
    Boot Up, 3-6,  , 4-2
    Brake
    Adjustment, 6-14
    Brake Arm
    Adjustment, 6-12
    Brake Pedal
    Replacement Procedure, 8-158
    Brakes
    Functional Checks, 4-23
    C
    Calibration Utilities, 7-34Caps lock
    display location, 4-7
    CE Compliance, 1-10
    CFM and PWD Modes
    Functional Checks, 4-9
    Cine
    Functional Checks, 4-12
    Cine gauge
    display location, 4-7
    Common Diagnostics, 7-44
    Configuration, 5-70
    Connectivity
    Worksheet, 3-16
    Contact Information, 1-11
    Control Panel, 4-5
    Cover, Upper and Lower Column
    Replacement Procedure, 8-166
    Customer Assistance, 1-11
    D
    Dangerous Procedure Warnings, 1-9
    Date/Time
    display location, 4-7
    Depth scale
    display location, 4-7
    Diagnostic
    Utilities, 7-33
    Diagnostic Groups, 7-22
    Diagnostic Utilities, 7-33
    Diagnostics, 5-67,  , 7-13
    Acquisition, 7-14
    Common, 7-44
    System-Level Analog, 7-29
    System-Level Digital, 7-28
    Direction Lock Pedal
    Replacement Procedure, 8-158
    Direction Locks
    Functional Checks, 4-23
    E
    EBM Board, 5-20
    ECG
    Functional Checks, 4-20
    Electrical
    requirements, 2-2
    Electrical Safety, 1-8
    Electrostatic Discharge Warning, 1-10
    EMC, 1-10
    INDEX 
    						
    							GE MEDICAL SYSTEMSPROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL   
    II  - 
    EMI, 1-10
    EMI Protection, 3-5
    EQ Board
    Basic Functions, 5-15
    General Description, 5-14
    EQ Diagnostics
    Board Level, 7-25
    Equalization (EQ) Board, 5-14
    ESD, 1-10
    Ethernet Signal, 5-49
    Exam study
    display location, 4-7
    External I/O, 5-46
    Bi-directional Signals, 5-47
    Input Signals, 5-47
    Location in the Unit, 5-46
    Output Signals, 5-49
    Replacement Procedure, 8-126
    F
    Fan Replacement Procedure, 8-122
    Focal zone
    display location, 4-7
    Front End Processor
    Power Supply Board, 5-5
    Simple Theory, 5-5
    Front End Subsystem, 5-6
    Front Panel
    Ending the Program, 7-43
    Front Panel Light, 7-43
    Testing the Front Panel Keys, 7-41
    Front Wheels Replacement Procedure, 8-151
    Functional Checks, 4-1
    B/M-Mode Checks, 4-8
    Basic Measurements, 4-10
    Brakes, 4-22,  , 4-23
    CFM and PWD Modes, 4-9
    Control Panel, 4-5
    ECG Checkout, 4-20
    Image Management, 4-13
    Locks, 4-23
    Mechanical, 4-22
    Monitor Display, 4-7
    Peripherals, 4-21
    Probes/Connector Usage, 4-11
    Required Equipment, 4-1
    Touch Panel, 4-6
    Using Cine, 4-12
    Using the MOD, 4-14
    G
    Gas Spring
    Adjustment, 6-6Gathering Trouble Data, 7-2
    General Cleaning, 10-9
    Gray/color bar
    display location, 4-7
    H
    Hazard Icons, 1-4
    Hospital name
    display location, 4-7
    Human Safety, 1-7
    I
    Image Management
    Functional Checks, 4-13
    Image management menu
    display location, 4-7
    Image preview
    display location, 4-7
    Imaging parameters
    display location, 4-7
    Inner Boss Bumper
    Removal Procedure, 8-164
    Inner Boss Crash Bumper
    Replacement Procedure, 8-165
    Inrush Current, 2-2
    InSite
    IP Address Configuration, 3-17
    Institution name
    display location, 4-7
    Internal I/O
    connections, 5-39
    Outputs, 5-43
    Replacement Procedure, 8-128
    K
    Keypad
    Replacement Procedure, 8-113
    L
    Label Locations, 1-8
    LEDs SCB, 5-12
    Left and Right Frog Leg Bumper
    Replacement Procedure, 8-162
    Logs, 5-64
    M
    Measurement summary window
    display location, 4-7
    Mechanical Checks 
    						
    							GE MEDICAL SYSTEMS PROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL 
     III
    Operator I/O, 4-22
    Mechanical Safety, 1-7
    Media
    Formatting, 4-15
    Memory
    Preferred Test Strategy, 7-37
    Minimum Cable Configuration, 7-59
    for System to Scan, 7-59
    MOD
    Functonal Checks, 4-14
    Models Covered, 1-2,  , 9-2
    Modem, 5-50
    Inputs/Outputs, 5-50
    LEDs, 5-50
    Location in the Unit, 5-50
    Monitor, 5-46
    Adjustment, 6-2
    Counter-balance Adjustment, 6-4
    Tilt, 6-4
    Tilt Adjustment, 6-4
    Monitor Display
    Functioanl Checks, 4-7
    Monitor display
    location, 4-7
    Monitor Troubleshooting, 7-61
    Move
    Archiving Images, 4-18
    O
    Operator I/O
    Emergency Release Procedure, 6-11
    Operator identification
    display location, 4-7
    P
    P4 Key Function, 7-4
    Patient I/O, 5-36
    Patient identification
    display location, 4-7
    Patient name
    display location, 4-7
    PC Diagnostics, 7-45
    Audio Test, 7-49
    CD/DVD Drive Test, 7-47
    CPU Tests, 7-45
    Hard Drive Tests, 7-46
    Keyboard Test, 7-49
    Memory Tests, 7-46
    Monitor Test, 7-49
    PCI Board Configuration Test, 7-48
    USB Test, 7-48
    Video Test, 7-47
    PC Diagnostics (Interactive Tests), 7-49PCI 9054 Interface, 7-35
    Preferred Test Strategy, 7-35
    PCVIC Card, 5-24
    Peripherals, 5-49
    Functional Checks, 4-21
    Physical Dimensions, 3-9
    Power Distribution, 5-52
    Basic Overall AC, 5-52
    Power Off, 3-7
    Procedure, 4-3
    Power On, 3-6,  , 4-2
    Power output readout
    display location, 4-7
    Power Requirements, 2-2
    electrical, 2-2
    stability, 2-3
    Power Stability Requirements, 2-3
    Power-up Procedures
    Voltage Settings, 3-5
    Prepearing the Unit for Installation, 3-5
    Probe Connector Cleaning, 10-11
    Probe identifier
    display location, 4-7
    Probe orientation marker
    display location, 4-7
    Probes, 3-15
    Disconnecting, 4-20
    Probes/Connector Usage
    Functional Checks, 4-11
    Product Icons, 1-5
    R
    Rear Crash Bumper
    Replacement Procedure, 8-163
    Rear Handle Replacement Procedure, 8-12
    Rear Wheel Brakes
    Adjustment, 6-15
    Rear Wheels Replacement Procedure, 8-147
    Receiving and Unpacking the Equipment, 3-4
    Regulatory, 6-1
    Release Lock Assembly
    Replacement Procedure, 8-102,  , 8-104
    Reliability Testing, 7-19
    Remote Software/Option Installation and Updates, 5-72
    Replacement Procedures
    AC Power, 8-89
    External I/O, 8-126
    Internal I/O, 8-128
    Top Cover, 8-8
    Upper Rear Cover, 8-7
    Restore
    Patient Database, 4-17
    Preset Configurations, 4-17
    RF Amplifier Board 
    						
    							GE MEDICAL SYSTEMSPROPRIETARY TO GE
    D
    IRECTION 2294854-100, REVISION 3  LOGIQ™ 9 PROPRIETARYMANUAL   
    IV  - 
    Theory, 5-8
    S
    Safety Considerations, 1-7
    Scan Control Board
    High Level Features, 5-12
    Scan Control Board (SCB), 5-11
    SCB Diagnostics
    Board Level, 7-22
    SCB LED, 5-12
    Screen Captures, 7-4
    Service Adjustments, 6-1
    Service Manual
    Purpose of, 1-1
    Shut Down
    Procedure, 4-3
    Shutdown, 3-7
    Side Covers
    Replacement Procedure, 8-5
    Stand-by Mode, 7-1
    System Does Not Boot, 7-51
    System Maintenance, 10-7
    System Manufacturer, 1-12
    System messages
    display location, 4-7
    System status (real-time or frozen)
    display location, 4-7
    System-Level Analog Diagnostics, 7-29
    System-Level Digital Diagnostics, 7-28
    T
    TD Board
    Diagnostics, 7-27
    TGC
    display location, 4-7
    Theory
    Front End SubSystem, 5-6
    General, 5-2
    RF Amplifier Board, 5-8
    XDIF Board, 5-7
    Time Delay (TD) Boards, 5-10
    Top Console, 5-45
    See Operator I/O, 5-45
    Top Cover
    Replacement Procedure, 8-8
    Top Plane Board, 5-7
    Touch Panel
    Functional Checks, 4-5,  , 4-6
    Trackball functionality status
    display location, 4-7
    Trouble Image with Logs, 7-3
    Troubleshooting
    Diagnostic Groups, 7-22Gathering Trouble Data, 7-2
    Screen Captures, 7-4
    Trouble Image with Logs, 7-3
    Vital System Information, 7-2
    Troubleshooting Trees, 7-50
    CD-RW, 7-67
    MOD, 7-68
    Network, 7-69
    Noise in Image, 7-56
    Printer Troubleshooting, 7-65
    System Does Not Power Off / Shutdown, 7-60
    System Does Not Power On / Boot Up, 7-50
    Trackball, 7-58
    Unable to Record to VCR, 7-64
    Unable to Scan, 7-57
    U
    Unpacking the Equipment, 3-4
    Upper Rear Cover
    Replacement Procedure, 8-7
    USB Adapter Setup, 5-28
    Utilities, 5-70
    V
    Video
    Specifications, 3-14
    Virtual Console Observation, 7-8
    Vital Product Data, 8-135
    Collecting, 8-135
    Voltage Settings, 3-5
    VPD
    How to Update, 8-137
    Vital Product Data
    Collecting, 8-135
    W
    Warnings and Cautions, 1-7
    Weight without Monitor and Peripherals, 3-9
    X
    XDIF Board
    Diagnostics, 7-27
    Theory, 5-7
    Z
    Z-Release Cable
    Adjustment, 6-6 
    						
    							GE Medical Systems
    GE Medical Systems:        Telex 3797371
    P.O. Box 414; Milwaukee, Wisconsin 53201, U.S.A.
    (Asia, Pacific, Latin America, North America)
    GE Ultraschall:Tel: +49 (0) 212 28 02 208
    Deutschland GmbH & Co KG
    Beethovenstrabe 239, Postfach 11 05 60
    D-42655 Solingen, German 
    						
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