BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 3252767 · Received July 25, 2013

    Report

    Report Number
    1720753-2013-08574
    Event Type
    Malfunction
    Date Received
    July 25, 2013
    Date of Event
    July 1, 2013
    Report Date
    July 25, 2013
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ONSITE INVESTIGATION. A POWER SUPPLY WIRE WAS REATTACHED. THE SYSTEM WAS THEN FOUND TO BE OPERATING AS INTENDED.

    Description of Event or Problem · 1

    THE FIELD ENGINEER REPORTED THAT THE SYSTEM WAS UNABLE TO PRODUCE X-RAY. THERE IS NO REPORT OF PT INJURY ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    349176 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1