BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6000032-1997-00032

    MDR report key: 83516 · Received April 9, 1997

    Report

    Report Number
    6000032-1997-00032
    Event Type
    Injury
    Date Received
    April 9, 1997
    Date of Event
    January 21, 1997
    Product Code
    GZB
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 MODEL 3888 LEAD LOT #L39869