BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1041124 · Received March 17, 2008

    Report

    Report Number
    1720753-2008-18048
    Event Type
    Malfunction
    Date Received
    March 17, 2008
    Date of Event
    March 5, 2008
    Report Date
    March 14, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE SERVICE REP ORDERED PART. ARRIVED ON SITE. REPLACED PS3. TESTED SYSTEM OPERATION. SYSTEM OPERATES AS INTENDED. CASE COMPLETE. NO FURTHER ACTIONS NECESSARY.

    Description of Event or Problem · 1

    CUSTOMER STATES COLUMN LIFT INTERMITTANTLY DOES NOT RISE. NO PTS WERE INJURED / INVOLVED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1