BEUDAMED
    FDA Registration Active 🇲🇽 Mexico

    DLP Single Stage Venous Cannula

    Reg #: 9617601 · FEI: 3002534070 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Medtronic Mexico S. de R.L. de CV
    Registration Number
    9617601
    FEI Number
    3002534070
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Av. Paseo Cucapah 10510 El Lago
    City
    Tijuana Baja California
    Country
    MX

    Regulatory Submissions

    510(k) Number
    K120988

    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
    Celia Encinas
    Address
    1610 Landmark Rd
    City
    San Diego
    State
    CA
    ZIP
    92154
    Country
    US
    Email
    [email protected]
    Phone
    949 7983913

    Products

    Device Name Product Code
    Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass DWF

    Proprietary Names

    DLP Single Stage Venous Cannula

    Establishment Types

    Manufacture Medical Device