BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2182596-1997-00304

    MDR report key: 87902 · Received April 30, 1997

    Report

    Report Number
    2182596-1997-00304
    Event Type
    Injury
    Date Received
    April 30, 1997
    Report Date
    April 3, 1997
    Product Code
    FTR
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention