BEUDAMED
    FDA Adverse Event Summary report: N

    ALLEGRETTO LASER

    MDR report key: 3209163 · Received June 28, 2013

    Report

    Report Number
    MW5030756
    Date Received
    June 28, 2013
    Date of Event
    September 22, 2011
    Report Date
    June 28, 2013
    Manufacturer
    WAVELIGHT LASER TECHNOLOGIE AG
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    HAD LASIK SURGERY WITH THE ALLEGRETTO SYSTEM AND NOW I HAVE SEVERE DRY EYE DISEASE. NO TREATMENT IS WORKING AND IT IS COSTING MY FAMILY TONS OF MONEY THAT I AM ON THE VERGE OF NOT WANTING TO LIVE ANYMORE, HELP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    294980 ALLEGRETTO LASER LASIK LASER LZS WAVELIGHT LASER TECHNOLOGIE AG

    Patients

    Seq Age Sex Outcome Treatment
    1 33 YR Other| S