BEUDAMED
    FDA Adverse Event Injury Summary report: N

    REZOOM

    MDR report key: 1032804 · Received April 21, 2008

    Report

    Report Number
    2648035-2008-00015
    Event Type
    Injury
    Date Received
    April 21, 2008
    Date of Event
    March 26, 2008
    Report Date
    March 26, 2008
    Manufacturer
    A.M.O.
    Product Code
    HQL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 REZOOM MULTIFOCAL INTRAOCULAR LENS HQL A.M.O. NXG1

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention