BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DPM 7

    MDR report key: 3091808 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-01053
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    April 15, 2013
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    MHX
    PMA / PMN Number
    092449
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    COMPANY REPRESENTATIVE EVALUATED THE UNIT. CORRECTION INCLUDED RECONNECTION OF THE LOOSE CABLE BETWEEN THE MAIN BOARD AND FRONT PANEL. PROBLEM RESOLVED.

    Description of Event or Problem · 1

    CUSTOMER REPORTED AN ISSUE BETWEEN THE DPM 7 MONITOR AND ITS PARAMETER MODULE, WHICH MAY HAVE AFFECTED PRIMARY MONITORING. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    188029 DPM 7 PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1