BEUDAMED
    FDA Adverse Event Other Summary report: N

    MORCHER ECR

    MDR report key: 556609 · Received August 31, 2004

    Report

    Report Number
    MW1033115
    Event Type
    Other
    Date Received
    August 31, 2004
    Date of Event
    August 27, 2004
    Report Date
    August 30, 2004
    Manufacturer
    MORCHER
    Product Code
    HQL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    INTRAOCULAR LENS AND ECR SUBLUXATION LEFT EYE SECONDARY TO BROKEN FIXATION SUTURE. PT UNDERWENT 8.0 GORTEX RESUTURING TO FIXATE IOL AND ECR IN 2004. NO COMPLICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MORCHER ECR ECR HQL MORCHER 12 070799

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Other