BEUDAMED
    FDA Adverse Event Other Summary report: N

    2021898-2003-00120

    MDR report key: 481797 · Received September 2, 2003

    Report

    Report Number
    2021898-2003-00120
    Event Type
    Other
    Date Received
    September 2, 2003
    Date of Event
    June 24, 2003
    Product Code
    JXG
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1