BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONMED CORPORATION

    MDR report key: 470283 · Received July 2, 2003

    Report

    Report Number
    1720159-2003-00063
    Event Type
    Malfunction
    Date Received
    July 2, 2003
    Date of Event
    May 6, 2003
    Report Date
    June 2, 2003
    Manufacturer
    CONMED ELECTROSURGERY
    Product Code
    GEI
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GR
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHEN THE DOCTOR TOUCHES THE FORCEPS WITH THE HANDSWITCHING PENCIL, MOST OF THE TIME THE DOCTOR GETS BURNED ON THE HAND WITH WHICH THE DOCTOR IS HOLDING THE FORCEPS.

    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