BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EYE SPHERE 20MM

    MDR report key: 364208 · Received November 28, 2001

    Report

    Report Number
    1920664-2001-00041
    Event Type
    Injury
    Date Received
    November 28, 2001
    Date of Event
    October 19, 2001
    Manufacturer
    BAUSCH & LOMB, INC.
    Product Code
    HPZ
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    53625 EYE SPHERE 20MM EYE SPHERE IMPLANT HPZ BAUSCH & LOMB, INC. NA S2297

    Patients

    Seq Age Sex Outcome Treatment
    1