BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONMED CORPORATION

    MDR report key: 377150 · Received February 13, 2002

    Report

    Report Number
    1720159-2002-00007
    Event Type
    Malfunction
    Date Received
    February 13, 2002
    Date of Event
    January 1, 2002
    Report Date
    January 17, 2002
    Manufacturer
    CONMED ELECTROSURGERY
    Product Code
    GEI
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUT BUTTON IS COAG AND THE COAG BUTTON IS CUT. NO INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED CORPORATION ELECTROSURGICAL UNIT GEI CONMED ELECTROSURGERY EXCALIBUR PLUS PC NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA NOT A CONTRIBUTOR TO THIS EVENT.| HAND-TROL, CATALOG# 60-2800-501, LOT# 01JHA002: