BEUDAMED
    FDA Adverse Event Injury Summary report: N

    *

    MDR report key: 136367 · Received December 4, 1997

    Report

    Report Number
    136367
    Event Type
    Injury
    Date Received
    December 4, 1997
    Report Date
    December 4, 1997
    Manufacturer
    PRECISION-COSMET
    Product Code
    HQL
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    RECURRENT HYPHEMAS RELATED TO AN IRIS PLANE INTRAOCULAR LENS OD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * Implant * HQL PRECISION-COSMET IC1331PA *

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention