BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CONMED CORPORATION

    MDR report key: 310478 · Received December 27, 2000

    Report

    Report Number
    1720159-2000-00099
    Event Type
    Injury
    Date Received
    December 27, 2000
    Date of Event
    November 24, 2000
    Report Date
    November 30, 2000
    Manufacturer
    CONMED/ASPEN LABS
    Product Code
    GEI
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BE
    Reporter Occupation
    OTHER

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other