BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    V60 VENTILATOR

    MDR report key: 8967316 · Received September 5, 2019

    Report

    Report Number
    2031642-2019-08183
    Event Type
    Malfunction
    Date Received
    September 5, 2019
    Report Date
    August 8, 2018
    Manufacturer
    RESPIRONICS CALIFORNIA, INC
    Product Code
    MNT
    PMA / PMN Number
    K082660
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DATE OF EVENT: (B)(6) 2018.DATE OF REPORT: 09/05/2019.THE FRONT BEZEL CASE AND NAV RING WERE REPLACED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED A FAILED NAVIGATION-RING (NAV-RING). THERE WAS NO PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    761802 V60 VENTILATOR VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE MNT RESPIRONICS CALIFORNIA, INC V60

    Patients

    Seq Age Sex Outcome Treatment
    1