BEUDAMED
    FDA Adverse Event Other Summary report: N

    SC60B-OUV

    MDR report key: 313320 · Received January 15, 2001

    Report

    Report Number
    1038833-2001-00001
    Event Type
    Other
    Date Received
    January 15, 2001
    Date of Event
    October 10, 2000
    Report Date
    January 5, 2001
    Manufacturer
    MEDICAL DEVELOPMENT RESEARCH, INC.
    Product Code
    HQL
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    LENS BECOMES CLOUDY OPACIFICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1541 SC60B-OUV POSTERIOR CHAMBER IOL HQL MEDICAL DEVELOPMENT RESEARCH, INC. SC60B-OUV AD16887

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR Disability