BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Cardioblate™ Gemini™

    Reg #: 3003955307 · FEI: 3003955307 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Medtronic Grand Rapids
    Registration Number
    3003955307
    FEI Number
    3003955307
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    620 Watson SW
    City
    Grand Rapids
    State
    MI
    ZIP
    49504
    Country
    US

    Regulatory Submissions

    510(k) Number
    K200514

    Owner / Operator

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

    Products

    Device Name Product Code
    Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue OCL

    Proprietary Names

    Cardioblate™ Gemini™

    Establishment Types

    Manufacture Medical Device