BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    IntelliVue Patient Monitor MX500, SW Rev. K.20

    Reg #: 9610816 · FEI: 3002807167 · Expires 2025
    View on FDA
    Products
    5
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    5

    Registration Details

    Registration Name
    Philips Medizin Systeme Boeblingen GmbH
    Registration Number
    9610816
    FEI Number
    3002807167
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    HEWLETT-PACKARD STRASSE 2
    City
    BOEBLINGEN Baden-Wurttemberg
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K141015

    Owner / Operator

    Firm Name
    Philips Medical Systems International BV
    Operator Number
    1217116
    Address
    Veenpluis 6
    City
    Best
    State
    NL-NOTA
    Postal Code
    5684PC
    Country
    NL

    US Agent

    Business Name
    Philips
    Contact Name
    Deborah Currlin
    Address
    222 Jacobs Street
    City
    Cambridge
    State
    MA
    ZIP
    02141
    Country
    US
    Email
    [email protected]
    Phone
    858 9452753

    Products

    Device Name Product Code
    Computer, Blood-Pressure DSK
    Analyzer, Spectrum, Electroencephalogram Signal GWS
    Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) MHX
    Alarm, Blood-Pressure DSJ
    Monitor, St Segment With Alarm MLD

    Proprietary Names

    IntelliVue Patient Monitor MX500, SW Rev. K.20 IntelliVue Patient Monitor MX550, SW Rev. K.20 IntelliVue Patient Monitor MX400, SW Rev. K.20 IntelliVue Patient Monitor MX450, SW Rev. K.20

    Establishment Types

    Manufacture Medical Device