BEUDAMED
    FDA Adverse Event Other Summary report: N

    2021898-2003-00043

    MDR report key: 451126 · Received March 26, 2003

    Report

    Report Number
    2021898-2003-00043
    Event Type
    Other
    Date Received
    March 26, 2003
    Date of Event
    December 9, 2002
    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