BEUDAMED
    FDA Adverse Event Other Summary report: N

    STRATUSOCT

    MDR report key: 585442 · Received March 18, 2005

    Report

    Report Number
    2918630-2005-00001
    Event Type
    Other
    Date Received
    March 18, 2005
    Date of Event
    February 14, 2005
    Report Date
    March 18, 2005
    Manufacturer
    CARL ZEISS MEDITEC INC
    Product Code
    HLI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    A PATIENT EXPERIENCED AN ELECTROSTATIC DISCHARGE WHILE TAKING AN EXAM. THE DISCHARGE OCCURRED IN THE VICINITY OF THE PATIENT'S EYE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRATUSOCT OPTICAL CORNEAL TOMOGRAPHY HLI CARL ZEISS MEDITEC INC 3000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other