BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GE OEC 9400

    MDR report key: 1232491 · Received November 13, 2008

    Report

    Report Number
    1720753-2008-28016
    Event Type
    Malfunction
    Date Received
    November 13, 2008
    Date of Event
    October 24, 2008
    Report Date
    November 10, 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

    A GE REPRESENTATIVE EVALUATED THE SYSTEM AND DETERMINED THE BATTERIES NEEDED TO BE REPLACED. CUSTOMER MUST ORDER THESE FROM A 3RD PARTY.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE SYSTEM WILL NOT TAKE X-RAYS. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE OEC 9400 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. 9400 NA

    Patients

    Seq Age Sex Outcome Treatment
    1