BEUDAMED
    FDA Adverse Event Other Summary report: N

    BRONCHOSCOPE

    MDR report key: 1921118 · Received December 8, 2010

    Report

    Report Number
    MW5018531
    Event Type
    Other
    Date Received
    December 8, 2010
    Date of Event
    November 8, 2010
    Report Date
    November 30, 2010
    Manufacturer
    OLYMPUS
    Product Code
    EOQ
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TROUBLE WITH SCOPE, AFTER FOLLOWING THE PROCEDURE WE WERE UNABLE TO SEE ANYTHING ON SCREEN. THE SCREEN SHOWED ONLY A DARK CLOUDY PICTURE. AFTER THE STAFF CHANGED SCOPES THE PICTURE WAS MUCH BETTER AND THE BRONCHOSCOPY WAS ABLE TO BE PERFORMED. THE SCOPE WAS RETURNED TO THE COMPANY FOR EVAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BRONCHOSCOPE EOQ OLYMPUS P40

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR