BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800MD

    MDR report key: 1083737 · Received July 29, 2008

    Report

    Report Number
    1720753-2008-24118
    Event Type
    Malfunction
    Date Received
    July 29, 2008
    Date of Event
    July 22, 2008
    Report Date
    July 29, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE CINE, HIGH CAPACITY DISK AND NETWORK FAIL MESSAGES DISPLAYED ON THE SYSTEM. NO PATIENT INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9800MD FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1