BEUDAMED
    FDA Adverse Event Other Summary report: N

    8010456-2006-00002

    MDR report key: 728811 · Received June 21, 2006

    Report

    Report Number
    8010456-2006-00002
    Event Type
    Other
    Date Received
    June 21, 2006
    Product Code
    LYJ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1