BEUDAMED
    FDA Adverse Event Other Summary report: N

    SC60B-OUV

    MDR report key: 297277 · Received September 14, 2000

    Report

    Report Number
    1038833-2000-00026
    Event Type
    Other
    Date Received
    September 14, 2000
    Date of Event
    September 14, 2000
    Report Date
    September 14, 2000
    Manufacturer
    MEDICAL DEVELOPMENT RESEARCH, INC.
    Product Code
    HQL
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    OPACIFICATION OF LENS. LENS BECAME CLOUDY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other