BEUDAMED
    FDA Adverse Event Injury Summary report: N

    9614385-2005-00067

    MDR report key: 617007 · Received June 22, 2005

    Report

    Report Number
    9614385-2005-00067
    Event Type
    Injury
    Date Received
    June 22, 2005
    Product Code
    FWN
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1