BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ASPEN SURGICAL SYSTEMS

    MDR report key: 302179 · Received October 12, 2000

    Report

    Report Number
    1720159-2000-00080
    Event Type
    Injury
    Date Received
    October 12, 2000
    Date of Event
    August 7, 2000
    Report Date
    September 14, 2000
    Manufacturer
    CONMED/ASPEN LABS
    Product Code
    GEI
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASPEN SURGICAL SYSTEMS GEI CONMED/ASPEN LABS HAND-TROL 96EHA011

    Patients

    Seq Age Sex Outcome Treatment
    1