BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HYDROVIEW INTRAOCULAR LENS

    MDR report key: 430975 · Received December 3, 2002

    Report

    Report Number
    1920664-2002-00352
    Event Type
    Injury
    Date Received
    December 3, 2002
    Date of Event
    October 30, 2002
    Report Date
    November 6, 2002
    Manufacturer
    BAUSCH & LOMB
    Product Code
    HQL
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IT
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    THE LENS WAS EXPLANTED DUE TO THE POSSIBLE CALCIFICATION. THE LENS WAS IMPLANTED ON 3/23/1999.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HYDROVIEW INTRAOCULAR LENS INTRAOCULAR LENS HQL BAUSCH & LOMB NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention