BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ASPEN SURGICAL SYSTEMS

    MDR report key: 39141 · Received September 17, 1996

    Report

    Report Number
    1720159-1996-00062
    Event Type
    Injury
    Date Received
    September 17, 1996
    Date of Event
    July 19, 1996
    Report Date
    September 17, 1996
    Manufacturer
    ASPEN LABORATORIES
    Product Code
    GEI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASPEN SURGICAL SYSTEMS ELECTROSURGICAL PENCIL GEI ASPEN LABORATORIES HANDTROL ELITE 96BHE008

    Patients

    Seq Age Sex Outcome Treatment
    1 *