BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DPM5 MONITOR

    MDR report key: 3091562 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00413
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    December 6, 2012
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    MHX
    PMA / PMN Number
    070791
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    MINDRAY SERVICE REPRESENTATIVES RESET THE MONITOR TO THE CORRECT SETTINGS AND RESOLVED THE ISSUE. PERFORMED ALL FUNCTIONAL AND SAFETY TESTS.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE DPM5 MONITOR DISPLAYED A CO2 COMMUNICATION ERROR WHICH MAY HAVE RESULTED IN A POSSIBLE LOSS OF CO2 MONITORING. NO REPORTS OF PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    187382 DPM5 MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1