BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GE 8800

    MDR report key: 1051341 · Received May 6, 2008

    Report

    Report Number
    9617766-2008-01108
    Event Type
    Malfunction
    Date Received
    May 6, 2008
    Date of Event
    April 24, 2008
    Report Date
    May 2, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ON SITE INVESTIGATION. THE PS3 POWER SUPPLY WAS REPLACED DURING THE SERVICE CALL. THE SYS WAS TESTED, AND FOUND TO BE WORKING AS INTENDED, AND PUT BACK INTO SERVICE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE VERTICAL LIFT COLUMN ON THE 8800 SYSTEM WOULD NOT WORK. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE 8800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1