BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Artix Thrombectomy Device

    Reg #: 3020347218 · FEI: 3020347218 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Inari Medical, Inc.
    Registration Number
    3020347218
    FEI Number
    3020347218
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    6001 Oak Canyon, Suite 100
    City
    Irvine
    State
    CA
    ZIP
    92618
    Country
    US

    Regulatory Submissions

    510(k) Number
    K220600

    Owner / Operator

    Firm Name
    STRYKER CORP.
    Operator Number
    1811755
    Address
    4100 East Milham Ave.
    City
    Kalamazoo
    State
    MI
    Postal Code
    49001
    Country
    US

    Products

    Device Name Product Code
    Catheter, Continuous Flush KRA
    Peripheral Mechanical Thrombectomy With Aspiration QEW

    Proprietary Names

    Artix Thrombectomy Device

    Establishment Types

    Manufacture Medical Device