BEUDAMED
    FDA Adverse Event Other Summary report: N

    9610617-2008-00019

    MDR report key: 1130743 · Received August 14, 2008

    Report

    Report Number
    9610617-2008-00019
    Event Type
    Other
    Date Received
    August 14, 2008
    Product Code
    GCJ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1