BEUDAMED
    FDA Adverse Event Death Summary report: N

    9610617-2000-00022

    MDR report key: 300044 · Received October 13, 2000

    Report

    Report Number
    9610617-2000-00022
    Event Type
    Death
    Date Received
    October 13, 2000
    Date of Event
    September 21, 2000
    Product Code
    KCD
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1