BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9600+

    MDR report key: 1183014 · Received October 3, 2008

    Report

    Report Number
    1720753-2008-25055
    Event Type
    Malfunction
    Date Received
    October 3, 2008
    Date of Event
    August 14, 2008
    Report Date
    August 25, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE SYSTEM WAS REPAIRED, FOUND TO BE OPERATING AS INTENDED, AND RELEASED TO THE CUSTOMER FOR USE. RESULTS- ERROR CODE DISPLAYED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM GIVES AN AD-ZERO ERROR. NO PT INVOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 9600+ FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS INC. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1