BEUDAMED
    FDA Adverse Event Other Summary report: N

    8031673-2005-00016

    MDR report key: 587888 · Received March 30, 2005

    Report

    Report Number
    8031673-2005-00016
    Event Type
    Other
    Date Received
    March 30, 2005
    Date of Event
    March 10, 2005
    Product Code
    JJE
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1