BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONMED CORPORATION

    MDR report key: 418545 · Received September 23, 2002

    Report

    Report Number
    1720159-2002-00126
    Event Type
    Injury
    Date Received
    September 23, 2002
    Date of Event
    August 23, 2002
    Report Date
    August 26, 2002
    Manufacturer
    CONMED ELECTROSURGERY
    Product Code
    GEI
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    INVALID DATA

    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 NOT CONTRIBUTE TO THIS EVENT.| CONMED PENCIL, CATALOG #130309, LOT #020424-1: DID