BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OPMI DRAPE

    MDR report key: 18042 · Received November 30, 1994

    Report

    Report Number
    MW1004198
    Event Type
    Malfunction
    Date Received
    November 30, 1994
    Report Date
    November 29, 1994
    Manufacturer
    CARL ZEISS, INC.
    Product Code
    HMW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE LENS, WHICH IS PART OF THE DRAPE, WAS SCRATCHED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OPMI DRAPE MICROSCOPE DRAPE HMW CARL ZEISS, INC. 2486

    Patients

    Seq Age Sex Outcome Treatment
    1 *