BEUDAMED
    FDA Registration Active 🇺🇸 United States

    EPIQ 5 Diagnostic Ultrasound System

    Reg #: 3017894900 · FEI: 3017894900 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    22
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    Philips Ultrasound LLC
    Registration Number
    3017894900
    FEI Number
    3017894900
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    222 Jacobs Street
    City
    Cambridge
    State
    MA
    ZIP
    02141
    Country
    US

    Regulatory Submissions

    510(k) Number
    K233545

    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

    Products

    Device Name Product Code
    Transducer, Ultrasonic, Diagnostic ITX
    System, Imaging, Pulsed Doppler, Ultrasonic IYN
    System, Imaging, Pulsed Echo, Ultrasonic IYO

    Proprietary Names

    EPIQ 5 Diagnostic Ultrasound System EPIQ 5W Diagnostic Ultrasound System EPIQ Elite Diagnostic Ultrasound System EPIQ CVx Circular Edition Ultrasound System EPIQ 5G Diagnostic Ultrasound System EPIQ 5C Diagnostic Ultrasound System EPIQ CVx Diagnostic Ultrasound System EPIQ CVxi Diagnostic Ultrasound System EPIQ Diagnostic Ultrasound System EPIQ 7G Diagnostic Ultrasound System EPIQ Elite W Diagnostic Ultrasound System Transducer X11-4t EPIQ CVx Diamond Select Ultrasound System EPIQ Elite Circular Edition Ultrasound System EPIQ 7C Diagnostic Ultrasound System EPIQ 5 Diamond Select Ultrasound System EPIQ 7 Diamond Select Ultrasound System EPIQ 7 Diagnostic Ultrasound System EPIQ 5 Circular Edition Ultrasound System EPIQ 7W Diagnostic Ultrasound System EPIQ 7 Circular Edition Ultrasound System EPIQ Elite Diamond Select Ultrasound System

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility