BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1043572-2001-00007

    MDR report key: 356342 · Received October 10, 2001

    Report

    Report Number
    1043572-2001-00007
    Event Type
    Malfunction
    Date Received
    October 10, 2001
    Date of Event
    August 22, 2001
    Product Code
    FSE
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    45712 FSE

    Patients

    Seq Age Sex Outcome Treatment
    1