BEUDAMED
    FDA Adverse Event Death Summary report: N

    9616026-2000-00004

    MDR report key: 296957 · Received September 21, 2000

    Report

    Report Number
    9616026-2000-00004
    Event Type
    Death
    Date Received
    September 21, 2000
    Date of Event
    August 24, 2000
    Product Code
    FII
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1