BEUDAMED
    FDA Registration Active 🇲🇽 Mexico

    Biosense Webster Inc

    Reg #: 9680001 · FEI: 3002808445 · Expires 2025
    View on FDA
    Products
    4
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    4

    Registration Details

    Registration Name
    Venusa de Mexico S. de R.L de C.V
    Registration Number
    9680001
    FEI Number
    3002808445
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    CALLE HERTZ 1525, Parque Industrial Antonio J. Bermudez
    City
    CIUDAD JUAREZ Chihuahua
    Country
    MX

    Regulatory Submissions

    PMA Number
    P990071

    Owner / Operator

    Firm Name
    Lake Region Medical
    Operator Number
    9048369
    Address
    340 Lake Hazeltine Drive
    City
    Chaska
    State
    MN
    Postal Code
    55318
    Country
    US

    US Agent

    Business Name
    Lake Region Medical
    Contact Name
    Paul Trnka
    Address
    340 Lake Hazeltine Drive, Bldg. C
    City
    Chaska
    State
    MN
    ZIP
    55318
    Country
    US
    Email
    [email protected]
    Phone
    952 6418396

    Products

    Device Name Product Code
    Cardiac Ablation Percutaneous Catheter LPB
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter OAD
    Catheter, Electrode Recording, Or Probe, Electrode Recording DRF

    Proprietary Names

    Biosense Webster Inc

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)