BEUDAMED
    FDA Adverse Event Other Summary report: N

    LUMENIS

    MDR report key: 480774 · Received August 21, 2003

    Report

    Report Number
    MW1029381
    Event Type
    Other
    Date Received
    August 21, 2003
    Date of Event
    April 24, 2003
    Report Date
    August 21, 2003
    Manufacturer
    LUMENIS, INC.
    Product Code
    GEX
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    FAILURE OF ZEISS MICROSCOPE EYE SAFETY FILTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LUMENIS ZEISS MICROSCOPE EYE SAFETY FILTER GEX LUMENIS, INC. NOVUS 2000 LASER 0627-068-01

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other