BEUDAMED
    FDA Registration Active 🇺🇸 United States

    DuraGraft

    Reg #: 3013508066 · FEI: 3013508066 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ARGONAUT MANUFACTURING SERVICES, INC.
    Registration Number
    3013508066
    FEI Number
    3013508066
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    2841 LOKER AVE E
    City
    Carlsbad
    State
    CA
    ZIP
    92010
    Country
    US

    Regulatory Submissions

    510(k) Number
    DEN230002

    Owner / Operator

    Firm Name
    Argonaut Manufacturing Services
    Operator Number
    10054547
    Address
    2841 Loker Avenue East
    City
    Carlsbad
    State
    CA
    Postal Code
    92010
    Country
    US
    Correspondent
    Leigh Amini

    Products

    Device Name Product Code
    Flushing Solution For Short Term Storage Of Veins At Room Temperature During Coronary Artery Bypass Graft Surgeries QEJ

    Proprietary Names

    DuraGraft

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)