BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HT70 PLUS VENTILATOR

    MDR report key: 3102604 · Received May 1, 2013

    Report

    Report Number
    2023050-2013-00366
    Event Type
    Malfunction
    Date Received
    May 1, 2013
    Date of Event
    April 13, 2013
    Report Date
    April 14, 2013
    Manufacturer
    NEWPORT MEDICAL INSTRUMENTS, INC.
    Product Code
    CBK
    PMA / PMN Number
    K111146
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    EG
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    REPORTEDLY, DURING SETUP, WHEN THE VENTILATOR WAS TURNED ON, THE TOUCH SCREEN WAS NON-FUNCTIONAL AND THE VENTILATOR COULD NOT BE OPERATED. THERE WAS NO PATIENT INVOLVEMENT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    190754 HT70 PLUS VENTILATOR CBK, NOU CBK NEWPORT MEDICAL INSTRUMENTS, INC. HT70PM

    Patients

    Seq Age Sex Outcome Treatment
    1