BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 1002747 · Received February 26, 2008

    Report

    Report Number
    1720753-2008-16405
    Event Type
    Malfunction
    Date Received
    February 26, 2008
    Date of Event
    February 19, 2008
    Report Date
    February 26, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    NO ADD'L INFO AT THIS TIME. WHEN ADD'L INFO IS PROVIDED, IT WILL BE REPORTED AS REQUIRED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE 9900 SYSTEM WILL NOT BOOT UP. THERE WAS NO REPORT OF PT INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. 9900 NA

    Patients

    Seq Age Sex Outcome Treatment
    1