BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONMED CORPORATION

    MDR report key: 405920 · Received July 18, 2002

    Report

    Report Number
    1720159-2002-00099
    Event Type
    Injury
    Date Received
    July 18, 2002
    Date of Event
    April 24, 2002
    Report Date
    June 21, 2002
    Manufacturer
    CONMED ELECTROSURGERY
    Product Code
    GEI
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED CORPORATION ABC LAPAROSCOPIC HANDPIECE GEI CONMED ELECTROSURGERY ABC PROBE 020228-1

    Patients

    Seq Age Sex Outcome Treatment
    1