BEUDAMED
    FDA Adverse Event Other Summary report: N

    2951239-1997-00002

    MDR report key: 108008 · Received July 23, 1997

    Report

    Report Number
    2951239-1997-00002
    Event Type
    Other
    Date Received
    July 23, 1997
    Date of Event
    June 3, 1997
    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