BEUDAMED
    FDA Registration Active 🇳🇱 Netherlands

    Subcutaneous Lead

    Reg #: 3003276151 · FEI: 3003276151 · Expires 2025
    View on FDA
    Products
    2
    Proprietary Names
    14
    Establishment Types
    1
    Classifications
    2

    Registration Details

    Registration Name
    Medtronic Bakken Research Center B.V. (BRC)
    Registration Number
    3003276151
    FEI Number
    3003276151
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Endepolsdomein 5
    City
    Maastricht Limburg
    Country
    NL

    Regulatory Submissions

    PMA Number
    P920015

    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
    Contact Name
    Carrie Schleis
    Address
    8200 Coral Sea St NE
    City
    Mounds View
    State
    MN
    ZIP
    55112
    Country
    US
    Email
    [email protected]
    Phone
    612 8101586

    Products

    Device Name Product Code
    Permanent Defibrillator Electrodes NVY
    Implantable Cardioverter Defibrillator (Non-Crt) LWS

    Proprietary Names

    Subcutaneous Lead Transvene Lead Transvene SVC Lead Adaptor Kit IS-1 Port Pin Plug Kit Tunneling Tool Sprint Quattro Secure Lead Adaptor Extender Kit Sprint Quattro Lead Sprint Quattro Secure S MRI SureScan Lead DF-1 Port Pin Plug Sprint Quattro Secure MRI SureScan Lead Sprint Quattro Secure S Lead Sprint Quattro MRI SureScan Lead

    Establishment Types

    Manufacture Medical Device