BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PENTAX

    MDR report key: 16588667 · Received March 22, 2023

    Report

    Report Number
    9610877-2023-52345
    Event Type
    Malfunction
    Date Received
    March 22, 2023
    Date of Event
    March 7, 2023
    Report Date
    March 22, 2023
    Manufacturer
    HOYA CORPORATION PENTAX TOKYO OFFICE
    Product Code
    FDF
    UDI-DI
    04961333234066
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THIS DEVICE IS CLASSIFIED AS IMPORT FOR EXPORT; THEREFORE, 510K IS NOT APPLICABLE. MODEL: EC34-I10TL-US IS AVAILABLE IN THE USA WITH A 510K NUMBER: K180285. THE PRODUCTS WAS RETURNED TO PENTAX MEDICAL FOR REPAIR. WE CHECKED THE RETURNED UNIT AND CONFIRMED THAT THE OBJECTIVE LENS FLUID DAMAGE. BASED ON THE RESULT, WE CONCLUDED THAT IT WAS CAUSED DUE TO THE FLUID DAMAGE FROM THE OBJECTIVE LENS. BASED ON THE TECHNICAL REPORT, ""HR-RPT-0586(IMAGE FAILURE)"" AND/OR THE RISK ANALYSIS RESULTS, IT WAS EVALUATED TO SUBMIT MDR. EMAIL: (B)(4).

    Description of Event or Problem · 0

    THE TIME OF EVENT IS NOT DURING PROCEDURE. THERE WAS NO REPORT OF PATIENT HARM. VIDEO IMAGE FAILURE (FLUID DAMAGE).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    825923 PENTAX VIDEO COLONOSCOPE FDF HOYA CORPORATION PENTAX TOKYO OFFICE EC34-I10TL 04961333234066

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown