BEUDAMED
    FDA Adverse Event Death Summary report: N

    6000032-2000-00057

    MDR report key: 264640 · Received February 18, 2000

    Report

    Report Number
    6000032-2000-00057
    Event Type
    Death
    Date Received
    February 18, 2000
    Date of Event
    January 7, 2000
    Product Code
    GZB
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GZB 7424 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Death