BEUDAMED
    FDA Adverse Event Death Summary report: N

    2182466-1999-00001

    MDR report key: 232737 · Received July 23, 1999

    Report

    Report Number
    2182466-1999-00001
    Event Type
    Death
    Date Received
    July 23, 1999
    Date of Event
    June 24, 1999
    Product Code
    DQA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1