BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PENTAX

    MDR report key: 14467842 · Received May 23, 2022

    Report

    Report Number
    9610877-2022-53800
    Event Type
    Malfunction
    Date Received
    May 23, 2022
    Date of Event
    April 25, 2022
    Report Date
    May 23, 2022
    Manufacturer
    HOYA CORPORATION PENTAX TOKYO OFFICE
    Product Code
    FET
    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 EPK-1000-US IS AVAILABLE IN THE USA WITH A 510K NUMBER K934918. WE CHECKED THE RETURNED UNIT AND CONFIRMED THAT THE PROCESS PCB AS DEFECTIVE. BASED ON THE RESULT, WE CONCLUDED THAT IT WAS CAUSED DUE TO THE EXCESSIVE SHOCK APPLIED ON THE PROCESS PCB. BASED ON THE TECHNICAL REPORT "HR-RPT-0586(IMAGE FAILURE)" AND/OR THE RISK ANALYSIS RESULTS, IT WAS EVALUATED TO SUBMIT MDR.

    Description of Event or Problem · 0

    THE TIME OF EVENT IS UNKNOWN. THERE WAS NO REPORT OF PATIENT HARM. VIDEO IMAGE FAILURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1642984 PENTAX SCOPEPILOT FET HOYA CORPORATION PENTAX TOKYO OFFICE NCU-7000

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown