BEUDAMED
    FDA Adverse Event Other Summary report: N

    ACUVUE OASYS

    MDR report key: 1040880 · Received February 26, 2008

    Report

    Report Number
    1033553-2008-00027
    Event Type
    Other
    Date Received
    February 26, 2008
    Report Date
    January 29, 2008
    Manufacturer
    VISTAKON
    Product Code
    LPL
    PMA / PMN Number
    P040045
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACUVUE OASYS SOFT CONTACT LENS LPL VISTAKON NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other