BEUDAMED
    FDA Adverse Event Summary report: N

    1933441-2002-00001

    MDR report key: 421671 · Received October 1, 2002

    Report

    Report Number
    1933441-2002-00001
    Date Received
    October 1, 2002
    Date of Event
    August 21, 2002
    Product Code
    FSA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1