BEUDAMED
    FDA Adverse Event Other Summary report: N

    8031673-2005-00018

    MDR report key: 617255 · Received May 17, 2005

    Report

    Report Number
    8031673-2005-00018
    Event Type
    Other
    Date Received
    May 17, 2005
    Date of Event
    April 5, 2005
    Product Code
    ---
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1