BEUDAMED
    FDA Adverse Event Other Summary report: N

    2021898-2002-00206

    MDR report key: 433403 · Received December 16, 2002

    Report

    Report Number
    2021898-2002-00206
    Event Type
    Other
    Date Received
    December 16, 2002
    Date of Event
    October 15, 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