BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MP40 INTELLIVUE PATIENT MONITOR

    MDR report key: 1931950 · Received December 13, 2010

    Report

    Report Number
    9610816-2010-00807
    Event Type
    Malfunction
    Date Received
    December 13, 2010
    Report Date
    November 15, 2010
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    MHX
    PMA / PMN Number
    K030038
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): THE CUSTOMER REPORTED A PROBLEM OF "ALARM ON THE SCOPE". NO PATIENT HARM WAS REPORTED. THE LIMITED AVAILABLE INFORMATION IS NOT SUFFICIENT TO SUPPORT OR RULE OUT THAT THERE WAS A PROBLEM WITH THE ALARM FUNCTION FOR THIS MONITOR. PHILIPS IS IN THE PROCESS OF OBTAINING ADDITIONAL INFORMATION CONCERNING THIS EVENT AND THE COMPLAINT IS STILL UNDER INVESTIGATION. A FINAL REPORT WILL BE SUBMITTED ONCE THE INVESTIGATION IS COMPLETED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED A PROBLEM OF "ALARM ON THE SCOPE". NO PATIENT HARM WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MP40 INTELLIVUE PATIENT MONITOR MHX PHILIPS MEDICAL SYSTEMS M8003A

    Patients

    Seq Age Sex Outcome Treatment
    1