BEUDAMED
    FDA Adverse Event Summary report: N

    3023859-2005-00001

    MDR report key: 613821 · Received June 7, 2005

    Report

    Report Number
    3023859-2005-00001
    Date Received
    June 7, 2005
    Date of Event
    April 18, 2005
    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