BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1213643-1997-00035

    MDR report key: 84431 · Received April 14, 1997

    Report

    Report Number
    1213643-1997-00035
    Event Type
    Injury
    Date Received
    April 14, 1997
    Date of Event
    November 22, 1996
    Product Code
    FTM
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1