BEUDAMED
    FDA Registration Active 🇨🇦 Canada

    Arctic Front Advance cardiac cryoablation catheter

    Reg #: 3002648230 · FEI: 3002648230 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Medtronic CryoCath LP
    Registration Number
    3002648230
    FEI Number
    3002648230
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    9000 Autoroute Transcanadienne
    City
    Pointe-Claire Quebec
    Country
    CA

    Regulatory Submissions

    PMA Number
    P100010

    Owner / Operator

    Firm Name
    Medtronic, Inc.
    Operator Number
    2112641
    Address
    710 Medtronic Parkway
    City
    Minneapolis
    State
    MN
    Postal Code
    55432
    Country
    US

    US Agent

    Business Name
    MEDTRONIC, INC.
    Contact Name
    Rashmi Bhushan
    Address
    8200 Coral Sea St NE, MVS33
    City
    Mounds View
    State
    MN
    ZIP
    55112
    Country
    US
    Email
    [email protected]
    Phone
    763 6070535

    Products

    Device Name Product Code
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE

    Proprietary Names

    Arctic Front Advance cardiac cryoablation catheter Freezor MAX cardiac cryoablation catheter Arctic Front Advance ProTM

    Establishment Types

    Manufacture Medical Device