BEUDAMED
    FDA Adverse Event Death Summary report: N

    2221819-1997-00731

    MDR report key: 122746 · Received September 26, 1997

    Report

    Report Number
    2221819-1997-00731
    Event Type
    Death
    Date Received
    September 26, 1997
    Date of Event
    June 7, 1997
    Manufacturer
    DATASCOPE CORP.
    Product Code
    DSP
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DSP DATASCOPE CORP. SYSTEM 90 NA

    Patients

    Seq Age Sex Outcome Treatment
    1