BEUDAMED
    FDA Adverse Event Other Summary report: N

    1030322-2002-00009

    MDR report key: 405941 · Received July 17, 2002

    Report

    Report Number
    1030322-2002-00009
    Event Type
    Other
    Date Received
    July 17, 2002
    Date of Event
    June 24, 2002
    Product Code
    FTF
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1