BEUDAMED
    FDA Adverse Event Death Summary report: N

    2221819-2001-00226

    MDR report key: 359962 · Received November 12, 2001

    Report

    Report Number
    2221819-2001-00226
    Event Type
    Death
    Date Received
    November 12, 2001
    Date of Event
    September 25, 2001
    Product Code
    DSP
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    50765 DSP

    Patients

    Seq Age Sex Outcome Treatment
    1