BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Subtle® Cannula

    Reg #: 2182291 · FEI: 2182291 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    VESTA
    Registration Number
    2182291
    FEI Number
    2182291
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    9900 S 57th St
    City
    Franklin
    State
    WI
    ZIP
    53132
    Country
    US

    Regulatory Submissions

    PMA Number
    P200002

    Owner / Operator

    Firm Name
    Vesta
    Operator Number
    10043140
    Address
    9900 S 57th St
    City
    Franklin
    State
    WI
    Postal Code
    53132
    Country
    US
    Correspondent
    Christopher Kobus

    Products

    Device Name Product Code
    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation OCM

    Proprietary Names

    Subtle® Cannula

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)