BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 1133723 · Received August 20, 2008

    Report

    Report Number
    1720753-2008-24877
    Event Type
    Malfunction
    Date Received
    August 20, 2008
    Date of Event
    August 8, 2008
    Report Date
    August 20, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM WOULD NOT TAKE A PICTURE. THE SYSTEM SHOWED A RECHARGE ERROR ON THE CARM DISPLAY. NO INJURY WAS REPORTED.

    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