BEUDAMED
    FDA Adverse Event Injury Summary report: N

    *

    MDR report key: 104453 · Received July 11, 1997

    Report

    Report Number
    9612007-1997-00013
    Event Type
    Injury
    Date Received
    July 11, 1997
    Date of Event
    June 9, 1997
    Report Date
    July 11, 1997
    Manufacturer
    ELEKTA IMPLANTS S.A.
    Product Code
    JXG
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * Implant JXG ELEKTA IMPLANTS S.A. NA 20996203

    Patients

    Seq Age Sex Outcome Treatment
    1 *