BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRC AC5000

    MDR report key: 1220658 · Received July 16, 2008

    Report

    Report Number
    1217116-2008-00048
    Event Type
    Malfunction
    Date Received
    July 16, 2008
    Date of Event
    January 25, 2008
    Report Date
    January 28, 2008
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    LLZ
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRC AC5000 LLZ (PICTURE ARCHIVING AND COMMUNICATIONS SYSTEM) LLZ PHILIPS MEDICAL SYSTEMS 73203 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *