BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221826-2008-00020

    MDR report key: 1131683 · Received August 14, 2008

    Report

    Report Number
    1221826-2008-00020
    Event Type
    Other
    Date Received
    August 14, 2008
    Product Code
    FFS
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1