BEUDAMED
    FDA Adverse Event Other Summary report: N

    1910735-2001-00002

    MDR report key: 351054 · Received September 5, 2001

    Report

    Report Number
    1910735-2001-00002
    Event Type
    Other
    Date Received
    September 5, 2001
    Date of Event
    August 9, 2001
    Product Code
    GFD
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    40122 GFD

    Patients

    Seq Age Sex Outcome Treatment
    1