BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GE OEC 9800

    MDR report key: 1030993 · Received April 17, 2008

    Report

    Report Number
    1720753-2008-20662
    Event Type
    Malfunction
    Date Received
    April 17, 2008
    Date of Event
    April 3, 2008
    Report Date
    April 14, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REPRESENTATIVE EVALUATED THE SYSTEM AND DETERMINED THE MONITOR NEEDED TO BE REPLACED. PART IS ON ORDER. IT IS ANTICIPATED, THE SYSTEM WILL BE RESTORED TO OPERATING AS INTENDED WHEN THE PART IS REPLACED.

    Description of Event or Problem · 1

    CUSTOMER REPORTED POOR IMAGE QUALITY. NO PATIENT INJURY WAS REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1