BEUDAMED
    FDA Adverse Event Other Summary report: N

    2518436-2005-00001

    MDR report key: 698707 · Received October 4, 2005

    Report

    Report Number
    2518436-2005-00001
    Event Type
    Other
    Date Received
    October 4, 2005
    Date of Event
    August 19, 2005
    Product Code
    BXY
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1