BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONMED CORPORATION

    MDR report key: 304178 · Received November 6, 2000

    Report

    Report Number
    1720159-2000-00083
    Event Type
    Malfunction
    Date Received
    November 6, 2000
    Date of Event
    October 5, 2000
    Report Date
    October 9, 2000
    Manufacturer
    CONMED/ASPEN LABS
    Product Code
    GEI
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    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 NA FOOTSWITCH-MFR UNK,| KLEPPINGER ENDOSCOPIC BIPOLAR FORCEPS,| MFG BY STORZ.