BEUDAMED
    FDA Adverse Event Death Summary report: N

    8022290-2001-00002

    MDR report key: 326063 · Received April 6, 2001

    Report

    Report Number
    8022290-2001-00002
    Event Type
    Death
    Date Received
    April 6, 2001
    Date of Event
    March 19, 2001
    Report Date
    April 5, 2001
    Product Code
    FNG
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    15446 FNG

    Patients

    Seq Age Sex Outcome Treatment
    1