BEUDAMED
    FDA Adverse Event Other Summary report: N

    CIBA VISION MEMORYLENS

    MDR report key: 378767 · Received February 22, 2002

    Report

    Report Number
    2648166-2002-00010
    Event Type
    Other
    Date Received
    February 22, 2002
    Report Date
    January 29, 2002
    Manufacturer
    CIBA VISION CORP
    Product Code
    HQL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    A REPORT REGARDING OPACIFICATION OF AN IOL WAS RECEIVED BY CIBA VISION ON 1/28/2002 FROM A SURGEON REGARDING A PT WHO HAD A MEMORYLENS IMPLANT IN 1999. NUMEROUS REQUESTS FOR ADDITIONAL INFO WERE MADE, BUT NOTHING WAS RECEIVED FROM THE SURGEON AT THE TIME OF THIS REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CIBA VISION MEMORYLENS INTRAOCULAR LENS HQL CIBA VISION CORP U940A *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other NONE REPORTED.