BEUDAMED
    FDA Adverse Event Death Summary report: N

    1933441-2001-00001

    MDR report key: 319481 · Received March 5, 2001

    Report

    Report Number
    1933441-2001-00001
    Event Type
    Death
    Date Received
    March 5, 2001
    Date of Event
    January 22, 2001
    Product Code
    FSA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    9348 FSA

    Patients

    Seq Age Sex Outcome Treatment
    1