BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 439383 · Received January 20, 2003

    Report

    Report Number
    MW1027305
    Event Type
    Other
    Date Received
    January 20, 2003
    Date of Event
    January 1, 2003
    Report Date
    January 20, 2003
    Manufacturer
    *
    Product Code
    LMO
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CORNEAL GRAFT REJECTION. CLOUDY GRAFT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * LMO * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Other