BEUDAMED
    FDA Adverse Event Death Summary report: N

    8010047-1997-00028

    MDR report key: 132025 · Received November 13, 1997

    Report

    Report Number
    8010047-1997-00028
    Event Type
    Death
    Date Received
    November 13, 1997
    Date of Event
    October 14, 1997
    Product Code
    FDF
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1