BEUDAMED
    FDA Adverse Event Other Summary report: N

    SC60B-0UV

    MDR report key: 242333 · Received September 24, 1999

    Report

    Report Number
    1038833-1999-00012
    Event Type
    Other
    Date Received
    September 24, 1999
    Date of Event
    May 1, 1999
    Manufacturer
    MFR
    Product Code
    HQL
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DESCRIBE EVENT OF PROBLEM: LENS BECOMES CLOUDY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SC60B-0UV Implant INTRAOCULAR LENS HQL MFR * A0-15804

    Patients

    Seq Age Sex Outcome Treatment
    1 *