BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIGASURE ADVANCE

    MDR report key: 2802702 · Received September 12, 2012

    Report

    Report Number
    2802702
    Event Type
    Malfunction
    Date Received
    September 12, 2012
    Date of Event
    August 30, 2012
    Report Date
    September 12, 2012
    Manufacturer
    COVIDIEN KENDALL
    Product Code
    GEI
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIGASURE ADVANCE ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI COVIDIEN KENDALL * 224827X

    Patients

    Seq Age Sex Outcome Treatment
    1 *