BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2132280-2005-00008

    MDR report key: 640517 · Received October 4, 2005

    Report

    Report Number
    2132280-2005-00008
    Event Type
    Injury
    Date Received
    October 4, 2005
    Date of Event
    September 16, 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