BEUDAMED
    FDA Adverse Event Other Summary report: N

    MORCHER CO

    MDR report key: 514441 · Received February 26, 2004

    Report

    Report Number
    MW1031362
    Event Type
    Other
    Date Received
    February 26, 2004
    Date of Event
    June 20, 2003
    Report Date
    February 16, 2004
    Manufacturer
    MORCHER CO.
    Product Code
    HQL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    SUBLUXED ECR OS AND IOL. ECR/XOL WERE REPOSITIONED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MORCHER CO 2L DEVICE HQL MORCHER CO. 2L 230798

    Patients

    Seq Age Sex Outcome Treatment
    1 36 YR Other