BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1810909-1996-00001

    MDR report key: 39975 · Received September 6, 1996

    Report

    Report Number
    1810909-1996-00001
    Event Type
    Malfunction
    Date Received
    September 6, 1996
    Date of Event
    July 12, 1996
    Product Code
    FMK
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1