BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COVIDIEN

    MDR report key: 1190207 · Received October 6, 2008

    Report

    Report Number
    MW5008548
    Event Type
    Malfunction
    Date Received
    October 6, 2008
    Date of Event
    September 17, 2008
    Report Date
    October 6, 2008
    Manufacturer
    COVIDIEN
    Product Code
    GDO
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE AUTOSUTURE ENDOCLIP ML WAS UNABLE TO BE USED AFTER ONLY TWO CLIPS WERE FIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COVIDIEN ENDOCLIP ML GDO COVIDIEN ENDOCLIP ML 10MM N8F216

    Patients

    Seq Age Sex Outcome Treatment
    1