BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221826-2008-00029

    MDR report key: 1289344 · Received December 4, 2008

    Report

    Report Number
    1221826-2008-00029
    Event Type
    Other
    Date Received
    December 4, 2008
    Product Code
    FFS
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1