BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 1140952 · Received September 3, 2008

    Report

    Report Number
    1720753-2008-24345
    Event Type
    Malfunction
    Date Received
    September 3, 2008
    Date of Event
    July 28, 2008
    Report Date
    August 6, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE GE SERVICE REP RESEATED THE GIB, FFB, AND HV SUPPLY REGULATOR. HE CHECKED THE MAIN BATTERIES AND INSPECTED THE INTERCONNECT CABLE. UNABLE TO DUPLICATE ERRORS.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE C-ARM DISPLAYS A LOW MA ERROR MESSAGE. NO PATIENT INJURY WAS REPORTED. THE CUSTOMER SWITCHED OUT THE C-ARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1