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GE Logiq 7 Service Manual

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    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    Section 1-2 - Important Conventions 1-19
    1-3-11 How to remove the Ghost CD-ROM
    The Ghost CD-ROM (Base System Software Load Image CD-ROM) is mounted on the PC-BOX inside 
    the scanner using velcro tapes. The upper side of the PC-BOX cover contains sharp edge causing a FE 
    to have possibility of cutting his hand if he removes the CD-ROM with the PC-BOX cover closed.
    Figure 1-6   How to Remove Ghost CD-ROM
    Ghost CD-ROM
    Sharp Edge
    PC-BOX Cover
    NG: WITH PC BOX COVER CLOSED
    OK: WITH PC BOX COVER OPEN
    PC-BOX Cover Do NOT remove the Ghost CD-ROM
    when the PC-Box cover is closed.
    For BT04 or laterCD-ROMs 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    1-20Section 1-2 - Important Conventions
    1-3-11 How to remove the Ghost CD-ROM (cont’d)
    The sharp edge of the PC Box Cover are chamfered before shipment. However, the Ghost CD-ROM 
    must be removed with the PC-Box cover open according to the following steps.
    1.) Disconnect the DVI-D connector, then remove the four mounting bolts (three hex bolts and one phillips screw).
    2.) Open the PC box cover and remove the Ghost CD-ROM from the PC box. Figure 1-7   Removing Bolts
    Figure 1-8   Removing Ghost CD-ROM
    Hex bolts
    PC Box CoverHex boltPhillips screw
    DVI-D connector
    PC Box Cover
    Open
    Ghost CD-ROM 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    Section 1-2 - Important Conventions 1-21
    Section 1-4
    EMC, EMI, and ESD
    1-4-1 Electromagnetic Compatibility
    Electro Magnetic 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 interface from its environment or 
    when the device produces unacceptable levels of mission to its environment. This interface is often 
    referred to as radio-frequency or electromagnetic interface (RFI/EMI) and can be radiated through 
    space or conducted over interconnecting power of 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.
    1-4-2 Electrostatic Discharge (ESD) Prevention
    1-4-3 CE Compliance
    The LOGIQ™ 7 unit conforms to all applicable conducted and radiated emission limits and immunity 
    from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient 
    requirements.
    Applicable standards are: 47CFR Part18, IEC60601-1-2, and 806-13.
    NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are  in good condition, 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.
    WARNINGWARNINGDO 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 dedicated ground point located on the rear of the scanner (to the left of the power 
    connector) or a proper frame ground.
    2.) Follow general guide lined for handling of electrostatic sensitive 
    equipment. 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    1-22Section 1-5 - Customer Assistance
    Section 1-5
    Customer Assistance
    This system is not repairable by the customer. If this equipment does not work as indicated in the 
    Operator Manual, please contact your service support center. If the service engineer needs additional 
    information to repair this equipment, please contact the following address (The necessary information 
    will be provided to the Service Engineer as needed).
    1-5-1 System Manufacture
    1-5-2 Contact Information
    For GE Service:  Table 1-6 System Manufacture
    GE YOKOGAWA MEDICAL SYSTEMS
    4-7-127 Asahigaoka, Hino-shi, Tokyo, 191-8503
    JAPAN
    Table 1-7 Phone Numbers for Customer Assistance
    LocationPhone Number
    USA/ Canada
    GE Medical Systems
    Ultrasound Service Engineering
    4855 W. Electric Avenue
    Milwaukee, WI 53219
    Customer Answer Center Tel: 1-800-321-7937
    1-800-682-5327
    1-262-524-5698
    Fax: +1-414-647-4125
    Latin America
    GE Medical Systems
    Ultrasound Service Engineering
    4855 W. Electric Avenue
    Milwaukee, WI 53219
    Customer Answer Center Tel: 1-262-524-5300
    1-262-524-5698
    Fax: +1-414-647-4125
    Europe
    GE Ultraschall Deutschland GmbH& Co. KG
    BeethovenstraBe 239
    Postfach 11 05 60, D-42655 Solingen
    Germany Tel:
    +33 0 130 831 300 - CARDIAC
    +33 0 130 831 300 - GENERAL IMAGING
    Fax: +49 212 2802 431
    Asia (Singapore)
    GE Ultrasound Asia
    Service Department - Ultrasound
    298 Tiong Bahru Road #15-01/06
    Central Plaza
    Singapore 169730 Tel: +65-6277-3512
    Fax: +65 6272-3997
    ASIA (Japan) +65-277-3512 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    Section 1-5 - Customer Assistance 1-23
    1-5-2 Contact Information (cont’d)
    NOTE: If this equipment does not work as indicated in the Operator Manual(s), contact your support  center. Have the system ID number available when you call. 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    1-24Section 1-5 - Customer Assistance
    This page was intentionally left blank. 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    Section 2-1 - Overview 2-1
    Chapter 2
    Pre Installation
    Section 2-1
    Overview
    2-1-1 Purpose of this chapter 2
    This chapter provides the information required to plan and prepare for the installation of a LOGIQ™ 7. 
    Included are descriptions of the facility and electrical needs to be met by the purchaser of the unit. A 
    checklist is also provided at the end of this section to help determine whether the proper planning and 
    preparation is accomplished before the actual equipment installation is scheduled.
    Table 2-1   Contents in Chapter 2
    SectionDescriptionPage Number
    2-1
    Overview 2-1
    2-2 General Console Requirements 2-2
    2-3 Facility Needs 2-7 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    2-2Section 2-2 - General Console Requirements
    Section 2-2
    General Console Requirements
    2-2-1 Console Environmental Requirements 
    2-2-1-1 Cooling
    The cooling requirement for the LOGIQ™ 7 is 3500 BTU/hr. This figure does not include cooling needed 
    for lights, people, or other equipment in the room. Each person in the room places an additional 300 
    BTU/hr. demand on the cooling system.
    2-2-1-2 Lighting Bright light is needed for system installation, updates and repairs. However, operator and patient 
    comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting 
    system (dim/bright) is recommended. Keep in mind that lighting controls and diameters can be a source 
    of EMI which could degrade image quality. These controls should be selected to minimize possible 
    interface. Table 2-2   Environmental Requirements for LOGIQ™ 7 Scanners
    OperationalStorageTransport
    Temperature
    10 - 35 oC
    50 - 95 oF -10 - 50 
    oC
    14 - 122oF -10 - 50 
    oC
    14 - 122 oF
    Humidity30 - 80%
    non-condensing 30 - 80%
    non-condensing30 - 80%
    non-condensing
    Pressure700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
    Table 2-3   Environmental Requirements for an Ultrasound Room
    ItemValues
    Power Source
    Refer to Table 2-4 on page 2-3.
    Current Rating20A (120V, 100V); 7.5A (220-240V) CIRCUIT BREAKER
    Radiation ShieldingNONE REQUIRED for ULTRASOUND ENERGY
    Temperature20-26 DEG. C (68-79 DEG F) for PATIENT COMFORT
    Humidity50% to 70% for PATIENT COMFORT
    Heat Dissipation3500 BTU/Hr. 
    Floor Landing Approximately 680 - 800 kg/m2 without Accessories
    Floor ConditionGradient: WITHIN 5 degrees
    WeightApproximately 225 kg (496lbs)   without Accessories 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    Section 2-2 - General Console Requirements 2-3
    2-2-2 Electrical Requirements
    2-2-2-1 Electrical 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 Line:
    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. 
    Please note that image artifacts can occur, if at any time within the facility, the ground from the 
    main facilitys incoming power source to the Ultrasound unit is only a conduit.
    2-2-2-2 LOGIQ™ 7 Power Requirements The following power line parameters should be monitored for one week before installation. We 
    recommend that you use an analyzer Dranetz Model 606-3 or Dranetz Model 626:
    2-2-2-3 Inrush Current Inrush Current is not a factor to consider due to the inrush current limiting properties of the power 
    supplies.
    2-2-2-4 Site Circuit Breaker It is recommended that the branch circuit breaker for the machine be ready accessible. Table 2-4   Electrical Specifications for LOGIQ™ 7
    PARAMETERAREALIMITS
    Voltage Range 100V
    100 VAC ±10% (90-110 VAC)
    220V 220-240 VAC ±10% (198-264 VAC)
    120V 120 VAC ±10% (108-132 VAC)
    PowerAll applicationsMAX. 1200 VA
    Line FrequencyAll applications50/60Hz ( ±2Hz)
    Power TransientsAll 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.
    Decaying Oscillation All applications Less than 15% of peak voltage for 
    less than 1 millisecond.
    CAUTIONPOWER OUTAGE MAY OCCURE. The LOGIQ™ 7 requi
    res 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. 
    						
    							GE HEALTHCARE
    DIRECTION 2286865, REVISION 14LOGIQ™ 7 SERVICE MANUAL
    2-4Section 2-2 - General Console Requirements
    2-2-2-5 Site Power Outlets
    A desiccated AC power outlet must be within reach of the unit without extension cords. Other outlets 
    adequate for the external peripherals, medical and test equipment needed to support this unit must also 
    be present within 1 m (3.2 ft.) of the unit. Electrical installation must meet all current local, state, and 
    national electrical codes.
    2-2-2-6 Unit Power Plug If the unit arrives without the power plug, or with the wrong plug, you must contact your GE dealer or 
    the installation engineer must supply what is locally required.
    2-2-2-7 Power Stability Requirements Voltage drop-out
    Max 10 ms.
    Power Transients
    Refer Table 
    						
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