BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1210157-1999-00016

    MDR report key: 233776 · Received July 27, 1999

    Report

    Report Number
    1210157-1999-00016
    Event Type
    Injury
    Date Received
    July 27, 1999
    Date of Event
    May 21, 1999
    Product Code
    GDW
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1