BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2182596-1996-00056

    MDR report key: 59458 · Received December 31, 1996

    Report

    Report Number
    2182596-1996-00056
    Event Type
    Injury
    Date Received
    December 31, 1996
    Date of Event
    December 2, 1996
    Product Code
    FTR
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1