BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 2193056 · Received July 22, 2011

    Report

    Report Number
    1720753-2011-20316
    Event Type
    Malfunction
    Date Received
    July 22, 2011
    Date of Event
    July 12, 2011
    Report Date
    July 22, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SVC REP PERFORMED A PHONE INVESTIGATION AND RECOMMENDED RESEATING THE FUSES ON THE POWER SUPPLY. NO CONCLUSION CAN BE DRAWN AS REPAIR INFO IS UNAVAILABLE AND NO ADD'L SVC INFO WAS PROVIDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYS WOULD NOT DISPLAY AN IMAGE ON THE MONITORS AND EXHIBITED NO OUTPUT AT THE POWER SUPPLY. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1