BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221826-2003-00008

    MDR report key: 459499 · Received May 9, 2003

    Report

    Report Number
    1221826-2003-00008
    Event Type
    Other
    Date Received
    May 9, 2003
    Date of Event
    April 3, 2003
    Product Code
    FGB
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1