BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    Refinity Rotational Intravascular Ultrasound (IVUS) Catheter

    Reg #: 3000126629 · FEI: 3000126629 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    2

    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
    K160583

    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
    Catheter, Ultrasound, Intravascular OBJ
    Transducer, Ultrasonic, Diagnostic ITX

    Proprietary Names

    Refinity Rotational Intravascular Ultrasound (IVUS) Catheter Refinity Short Tip Rotational Intravascular Ultrasound (IVUS) Catheter

    Establishment Types

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