BEUDAMED
    FDA Adverse Event Death Summary report: N

    2182466-2003-00001

    MDR report key: 437223 · Received January 10, 2003

    Report

    Report Number
    2182466-2003-00001
    Event Type
    Death
    Date Received
    January 10, 2003
    Date of Event
    September 20, 2002
    Product Code
    DSA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1