BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DPM 6 MONITOR

    MDR report key: 3091268 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00584
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    February 13, 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
    MN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    MINDRAY SERVICE REPS WERE UNABLE TO DUPLICATE THE ISSUES.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE SPO2 ALARMS FOR LOW SPO2 WHEN READINGS ARE WITHIN LIMITS. UNIT ALARMS FOR ASYSTOLE WHEN A NORMAL ECG IS DISPLAYED ON THE SCREEN. NOISY ECG WAVEFORM. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    186748 DPM 6 MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1