BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MENTOR ORC INTRAOCULAR LENS

    MDR report key: 48988 · Received November 5, 1996

    Report

    Report Number
    1220108-1996-00287
    Event Type
    Malfunction
    Date Received
    November 5, 1996
    Date of Event
    October 17, 1996
    Report Date
    October 18, 1996
    Manufacturer
    MENTOR OPHTHALMICS, INC.
    Product Code
    HQL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    HAPTIC BROKE WHILE INSERTION. PER INFORMATION FROM PHYSICIAN, THERE WAS NO TRAUMA TO PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MENTOR ORC INTRAOCULAR LENS Implant IOL HQL MENTOR OPHTHALMICS, INC. C455F N0952

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO