BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GE OEC 7700

    MDR report key: 1033127 · Received April 23, 2008

    Report

    Report Number
    9680959-2008-00066
    Event Type
    Injury
    Date Received
    April 23, 2008
    Date of Event
    April 10, 2008
    Report Date
    April 22, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS, INC
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE OEC 7700 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS, INC 7700 NA

    Patients

    Seq Age Sex Outcome Treatment
    1