BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIGASURE

    MDR report key: 18777000 · Received February 26, 2024

    Report

    Report Number
    18777000
    Event Type
    Other
    Date Received
    February 26, 2024
    Date of Event
    February 6, 2024
    Report Date
    February 9, 2024
    Manufacturer
    COVIDIEN LP
    Product Code
    GEI
    UDI-DI
    10884521521735
    Report Source
    User Facility report
    Reporter Location
    TN
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    DEVICE SENT TO RISK MANAGEMENT FOR REPORTING. NO REPORT STATING THE MALFUNCTION OR BREAK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    348956 LIGASURE ELECTROSURGICAL, CUTTING COAGULATION ACCESSORIES GEI COVIDIEN LP LF5637 30880234X 10884521521735

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Male