BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1992879 · Received February 5, 2011

    Report

    Report Number
    1720753-2011-00963
    Event Type
    Malfunction
    Date Received
    February 5, 2011
    Date of Event
    October 18, 2010
    Report Date
    February 5, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TU
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER REFORMATTED THE HARD DRIVE AND CLEARED THE FAULT. NO GE SERVICE WAS PERFORMED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE SYSTEM IS NOT WORKING. 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