BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZEISS MICROSCOPE

    MDR report key: 1311803 · Received February 4, 2009

    Report

    Report Number
    1311803
    Event Type
    Malfunction
    Date Received
    February 4, 2009
    Date of Event
    February 4, 2009
    Report Date
    February 4, 2009
    Manufacturer
    CARL ZEISS, INC.
    Product Code
    EPT
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    DE, US

    Narratives

    Description of Event or Problem · 1

    MICROSCOPE MALFUNCTIONED IN THE MIDDLE OF THE CASE. MD UNABLE TO FINISH CASE AND WILL REQUIRE THE RETURN OF THE PATIENT TO THE OR TO COMPLETE PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZEISS MICROSCOPE MICROSCOPE, SURGICAL EPT CARL ZEISS, INC. CTS 294060 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *