BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASERSCAN LSX EXCIMER LASER

    MDR report key: 384834 · Received February 27, 2002

    Report

    Report Number
    1058106-2002-00001
    Event Type
    Injury
    Date Received
    February 27, 2002
    Date of Event
    February 23, 2002
    Manufacturer
    LASERSIGHT TECHNOLOGIES, INC.
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    BILATERAL DECENTRATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASERSCAN LSX EXCIMER LASER EXCIMER LASER FOR CORRECTING REFRACTIVE ERRORS LZS LASERSIGHT TECHNOLOGIES, INC. 66040019 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 19 YR