BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1921846-1998-00020

    MDR report key: 190325 · Received October 5, 1998

    Report

    Report Number
    1921846-1998-00020
    Event Type
    Injury
    Date Received
    October 5, 1998
    Date of Event
    September 9, 1998
    Product Code
    GAN
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 Implant GAN

    Patients

    Seq Age Sex Outcome Treatment
    1