BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2021898-1999-00078

    MDR report key: 227006 · Received May 28, 1999

    Report

    Report Number
    2021898-1999-00078
    Event Type
    Malfunction
    Date Received
    May 28, 1999
    Date of Event
    April 22, 1999
    Product Code
    JXG
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1