BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    EPIQ Diagnostic Ultrasound System

    Reg #: 3000126629 · FEI: 3000126629 · Expires 2025
    View on FDA
    Products
    3
    Proprietary Names
    24
    Establishment Types
    1
    Classifications
    3

    Registration Details

    Registration Name
    Philips Electronics Ltd
    Registration Number
    3000126629
    FEI Number
    3000126629
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1875 Buckhorn Gate, 5th Floor
    City
    Mississauga Ontario
    Country
    CA

    Regulatory Submissions

    510(k) Number
    K200304

    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
    Shaylee Masilunas
    Address
    6501 Living Place
    City
    Pittsburgh
    State
    PA
    ZIP
    15206
    Country
    US
    Email
    [email protected]
    Phone
    724 8162019

    Products

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

    Proprietary Names

    EPIQ Diagnostic Ultrasound System EPIQ 7G Diagnostic Ultrasound System EPIQ 5W Diagnostic Ultrasound System L12-5; L15-7io; L18-5 EPIQ CVxi Diagnostic Ultrasound System EPIQ 5C Diagnostic Ultrasound System V6-2; V9-2; VL13-5 EPIQ 5G Diagnostic Ultrasound System eL18-4; eL18-4 EMT L12-3; L12-3ERGO 3D9-3v EPIQ 7W Diagnostic Ultrasound System EPIQ Elite Diagnostic Ultrasound System C10-4ec; D2cwc mC7-2; mC12-3 EPIQ CVx Diagnostic Ultrasound System S4-2; S5-1 X5-1; X6-1; X7-2; X7-2t ; X8-2t; XL14-3 S7-3t; S8-3;S8-3t; S9-2 EPIQ 7C Diagnostic Ultrasound System D2tcd; D5cwc C5-1; C6-2; C8-5; C9-2; C10-3v EPIQ 7 Diagnostic Ultrasound System EPIQ 5 Diagnostic Ultrasound System

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device