BEUDAMED
    FDA Registration Active 🇬🇧 United Kingdom

    CoreVista® Retractor

    Reg #: 3023190433 · FEI: 3023190433 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    CARDIOPRECISION LTD
    Registration Number
    3023190433
    FEI Number
    3023190433
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Innovation Centre, 1 Ainslie Road, Hillington
    City
    Glasgow Lancashire
    Country
    GB

    Owner / Operator

    Firm Name
    CardioPrecision Ltd
    Operator Number
    10085327
    Address
    Innovation Centre, 1 Ainslie Road, Hillington
    City
    Glasgow
    State
    Renfrewshire
    Postal Code
    G52 4RU
    Country
    GB
    Correspondent
    Ying Sutherland

    US Agent

    Business Name
    State of the Art Medical Products, Inc.
    Contact Name
    Keith Lambie
    Address
    41 Canfield Rd
    City
    Cedar Grove
    State
    NJ
    ZIP
    07009
    Country
    US
    Email
    [email protected]
    Phone
    973 5712400

    Products

    Device Name Product Code
    Instruments, Surgical, Cardiovascular DWS

    Proprietary Names

    CoreVista® Retractor CoreVista® Retractor System

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility