BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EXE-60 POSTERIOR INTRAOCULAR LENS

    MDR report key: 810234 · Received January 11, 2007

    Report

    Report Number
    1920664-2007-00048
    Event Type
    Malfunction
    Date Received
    January 11, 2007
    Date of Event
    December 12, 2006
    Manufacturer
    BAUSCH & LOMB, INC.
    Product Code
    HQL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE HAPTIC OF THE LENS WAS FOUND DAMAGED UPON RECEIPT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 EXE-60 POSTERIOR INTRAOCULAR LENS INTRAOCULAR LENS HQL BAUSCH & LOMB, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *