BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INTELLIVUE CLINICAL INFORMATION PORTFOLIO (ICIP)

    MDR report key: 3090258 · Received April 19, 2013

    Report

    Report Number
    1218950-2013-01437
    Event Type
    Malfunction
    Date Received
    April 19, 2013
    Report Date
    March 21, 2013
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    DXJ
    PMA / PMN Number
    K992636
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT DESPITE A DRUG BEING PRESCRIBED AT 18.05 HRS, THE FIRST SCHEDULED DOSE WAS NOT AVAILABLE UNTIL THE NEXT DAY. NO PATIENT HARM WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    169493 INTELLIVUE CLINICAL INFORMATION PORTFOLIO (ICIP) DXJ PHILIPS MEDICAL SYSTEMS 865047

    Patients

    Seq Age Sex Outcome Treatment
    1