BEUDAMED
    FDA Adverse Event Other Summary report: N

    CONMED CORPORATION

    MDR report key: 515091 · Received March 5, 2004

    Report

    Report Number
    1720159-2004-00005
    Event Type
    Other
    Date Received
    March 5, 2004
    Date of Event
    January 1, 2004
    Report Date
    March 4, 2004
    Manufacturer
    CONMED ELECTROSURGERY
    Product Code
    GEI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THE DRAPE CAUGHT ON FIRE DURING A PROCEDURE AND THE PT WAS BURNED. THEY STATED THAT THE INJURY WAS NOT ANYTHING EXTENSIVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED CORPORATION ESU SYSTEM 6500 GEI CONMED ELECTROSURGERY * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention