BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6000036-1999-00075

    MDR report key: 233799 · Received July 29, 1999

    Report

    Report Number
    6000036-1999-00075
    Event Type
    Injury
    Date Received
    July 29, 1999
    Date of Event
    June 24, 1999
    Product Code
    DTK
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1