BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DPM 6/7 PATIENT MONITOR

    MDR report key: 3832086 · Received March 7, 2014

    Report

    Report Number
    2221819-2014-00064
    Event Type
    Malfunction
    Date Received
    March 7, 2014
    Date of Event
    February 7, 2014
    Report Date
    February 7, 2014
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    MHX
    PMA / PMN Number
    092449
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    PRODUCT IS BEING RETURNED FOR EVAL.

    Description of Event or Problem · 1

    CUSTOMER REPORTED AN ISSUE WITH THE DPM 6/7 MONITOR'S MPM MODULE WHICH MAY HAVE AFFECTED PT MONITORING. THERE WAS NO PT INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    138681 DPM 6/7 PATIENT MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1