BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2523676-2008-00376

    MDR report key: 1051459 · Received May 16, 2008

    Report

    Report Number
    2523676-2008-00376
    Event Type
    Injury
    Date Received
    May 16, 2008
    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