BEUDAMED
    FDA Adverse Event Death Summary report: N

    1044265-2000-00013

    MDR report key: 273865 · Received April 17, 2000

    Report

    Report Number
    1044265-2000-00013
    Event Type
    Death
    Date Received
    April 17, 2000
    Date of Event
    March 18, 2000
    Report Date
    March 18, 2000
    Product Code
    CAH
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 Death