BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MORCHER COLOBOMA RING

    MDR report key: 1373659 · Received May 1, 2009

    Report

    Report Number
    MW5010943
    Event Type
    Injury
    Date Received
    May 1, 2009
    Date of Event
    April 13, 2009
    Report Date
    April 28, 2009
    Manufacturer
    MORCHER GMBH
    Product Code
    MRJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT HAD CATARACT SURGERY WITH IMPLANTATION OF MORCHER 96F RING AND PUPILLOPLASTY IN 2008; SURGERY WAS UNEVENTFUL AND RECOVERY GOOD (RIGHT EYE). PT PRESENTED IN 2009, WITH A RETINAL DETACHMENT RIGHT EYE; BOTH MYSELF AND THE CONSULTING RETINA SURGEON DO NOT FEEL THE USE OF THE DEVICE IN RELATED TO THE SUBSEQUENT RETINAL DETACHMENT. OD RETINAL DETACHMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MORCHER COLOBOMA RING CAPSULAR RING WITH A PERTURE MRJ MORCHER GMBH TYPE 96F AJEBFD

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Required Intervention