BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1173018 · Received September 19, 2008

    Report

    Report Number
    1720753-2008-26119
    Event Type
    Malfunction
    Date Received
    September 19, 2008
    Date of Event
    September 8, 2008
    Report Date
    September 19, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE GE SERVICE REP WAS UNABLE TO DUPLICATE THE ERROR. HOWEVER, THEY NOTED AN ERROR IN LOGS. THE WAS ZEROED MA NULL ADJUSTMENT PERFORMED FILAMENT CALIBRATION. SYSTEM TESTS SATISFACTORY AT THIS TIME WITH NO LO MA ERRORS DISPLAYED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED INTERMITTENT LOW MA ERROR. A MA AND FILAMENT CALIBRATION WERE PERFORMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1