BEUDAMED
    FDA Adverse Event Summary report: N

    VISEX LASER

    MDR report key: 27040 · Received October 5, 1995

    Report

    Report Number
    MW4000820
    Date Received
    October 5, 1995
    Report Date
    June 22, 1995
    Manufacturer
    VISION SCULPING
    Product Code
    HQF
    Report Source
    Voluntary report
    Reporter Location
    NM, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    SEMINARS ARE BEING SPONSORED PROMOTING LASER EYE SURGERY WITH THE LASER. THEN SENDS PTS TO CANADA TO HAVE SURGERY PERFORMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VISEX LASER LASER HQF VISION SCULPING

    Patients

    Seq Age Sex Outcome Treatment
    1 *