BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OPMI

    MDR report key: 936257 · Received August 27, 2004

    Report

    Report Number
    2431026-2004-00002
    Event Type
    Malfunction
    Date Received
    August 27, 2004
    Date of Event
    August 2, 2004
    Report Date
    August 26, 2004
    Manufacturer
    CARL ZEISS, INC.
    Product Code
    EPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *