BEUDAMED
    FDA Adverse Event Death Summary report: N

    ASPEN SURGICAL SYSTEMS

    MDR report key: 282424 · Received June 14, 2000

    Report

    Report Number
    1720159-2000-00048
    Event Type
    Death
    Date Received
    June 14, 2000
    Date of Event
    May 16, 1900
    Report Date
    May 17, 2000
    Manufacturer
    CONMED/ASPEN LABS
    Product Code
    GEI
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASPEN SURGICAL SYSTEMS ELECTROSURGICAL PENCIL GEI CONMED/ASPEN LABS HAND-TROL 99KHA006

    Patients

    Seq Age Sex Outcome Treatment
    1