BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Thruport Endoclamp Aortic Catheters

    Reg #: 3008500478 · FEI: 1713910 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Edwards Lifesciences LLC
    Registration Number
    3008500478
    FEI Number
    1713910
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    12050 Lone Peak Parkway
    City
    Draper
    State
    UT
    ZIP
    84020
    Country
    US

    Regulatory Submissions

    510(k) Number
    K962510

    Owner / Operator

    Firm Name
    Edwards Lifesciences LLC
    Operator Number
    9040666
    Address
    One Edwards Way
    City
    Irvine
    State
    CA
    Postal Code
    92614
    Country
    US
    Correspondent
    Denny Kouri

    Products

    Device Name Product Code
    Clamp, Vascular DXC

    Proprietary Names

    Thruport Endoclamp Aortic Catheters

    Establishment Types

    Manufacture Medical Device