BEUDAMED
    FDA Adverse Event Death Summary report: N

    8022290-2001-00001

    MDR report key: 314674 · Received January 25, 2001

    Report

    Report Number
    8022290-2001-00001
    Event Type
    Death
    Date Received
    January 25, 2001
    Date of Event
    January 8, 2001
    Report Date
    January 24, 2001
    Product Code
    FNL
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3099 FNL

    Patients

    Seq Age Sex Outcome Treatment
    1