BEUDAMED
    FDA Adverse Event Other Summary report: N

    8010461-2005-00001

    MDR report key: 603996 · Received May 13, 2005

    Report

    Report Number
    8010461-2005-00001
    Event Type
    Other
    Date Received
    May 13, 2005
    Product Code
    LXH
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1