BEUDAMED
    FDA Adverse Event Death Summary report: N

    2523148-1998-00001

    MDR report key: 201398 · Received December 10, 1998

    Report

    Report Number
    2523148-1998-00001
    Event Type
    Death
    Date Received
    December 10, 1998
    Date of Event
    October 18, 1998
    Product Code
    CAX
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1