BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1831901 · Received September 8, 2010

    Report

    Report Number
    1720753-2010-02970
    Event Type
    Malfunction
    Date Received
    September 8, 2010
    Date of Event
    August 20, 2010
    Report Date
    September 8, 2010
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REP EVALUATED THE SYSTEM AND COULD NOT REPRODUCE THE REPORTED PROBLEM. GE REP INFORMED CUSTOMER THAT THE FAILURE WAS PROBABLY CAUSED BY THE BATTERIES NOT BEING CHARGED BEFORE USE. SYSTEM OPERATES AS INTENDED.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THAT AFTER A SHORT FLUORO TIME, THE IMAGES FADED OUT. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1