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