BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 3241049 · Received July 18, 2013

    Report

    Report Number
    1720753-2013-08290
    Event Type
    Malfunction
    Date Received
    July 18, 2013
    Date of Event
    July 4, 2013
    Report Date
    July 18, 2013
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO CONCLUSION CAN BE DRAWN AS REPAIR INFORMATION IS UNAVAILABLE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED AN INTERNAL SYSTEM ERROR APPEARS AND IT FREEZES, LOCK UP. THERE IS NO REPORT OF PATIENT INJURY OR DEATH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    336430 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1