BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9600

    MDR report key: 2192887 · Received July 25, 2011

    Report

    Report Number
    1720753-2011-20350
    Event Type
    Malfunction
    Date Received
    July 25, 2011
    Date of Event
    July 14, 2011
    Report Date
    July 25, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN OVER THE PHONE INVESTIGATION. THE SYSTEM CANNOT BE REPAIRED AS THE REQUIRED PARTS TO MAKE THE REPAIR ARE NO LONGER AVAILABLE. THE SYSTEM WAS PUT BACK INTO SERVICE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM WOULD NOT SAVE IMAGES. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9600 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9600

    Patients

    Seq Age Sex Outcome Treatment
    1