BEUDAMED
    FDA Registration Active 🇺🇸 United States

    BRK-1™ Transseptal Needle 407207

    Reg #: 2182269 · FEI: 2182269 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    12
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    St. Jude Medical, Atrial Fibrillation Division, Inc.
    Registration Number
    2182269
    FEI Number
    2182269
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    14901 DEVEAU PL.
    City
    Minnetonka
    State
    MN
    ZIP
    55345
    Country
    US

    Owner / Operator

    Firm Name
    ABBOTT LABORATORIES
    Operator Number
    1415939
    Address
    100 ABBOTT PARK RD., D-03Q3, AP52-1
    City
    Abbott Park
    State
    IL
    Postal Code
    60064
    Country
    US

    Products

    Device Name Product Code
    Trocar DRC

    Proprietary Names

    BRK-1™ Transseptal Needle 407207 BRK-1™ Transseptal Needle 407201 BRK™ XS Series Transseptal Needle G407208 BRK™ XS Series Transseptal Needle G407211 BRK Transseptal Needle G407215 BRK-1™ XS Series Transseptal Needle G407216 BRK-1™ XS Series Transseptal Needle G407209 BRK™ Transseptal Needle 407206 BRK™ XS Series Transseptal Needle G407210 BRK™ Transseptal Needle 407205 BRK-1™ XS Series Transseptal Needle G407212 BRK™ Transseptal Needle 407200

    Establishment Types

    Develop Specifications But Do Not Manufacture At This Facility