BEUDAMED
    FDA Registration Active 🇧🇪 Belgium

    LifeStent 5F Vascular Stent System

    Reg #: 3002504068 · FEI: 3002504068 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    3
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Bard European Distribution Center NV
    Registration Number
    3002504068
    FEI Number
    3002504068
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    Hagelberg 2
    City
    Olen Antwerpen
    Country
    BE

    Regulatory Submissions

    PMA Number
    P070014

    Owner / Operator

    Firm Name
    C. R. Bard, Inc.
    Operator Number
    2212754
    Address
    1 Becton Drive
    City
    Franklin Lakes
    State
    NJ
    Postal Code
    07417
    Country
    US

    Products

    Device Name Product Code
    Stent, Superficial Femoral Artery NIP

    Proprietary Names

    LifeStent 5F Vascular Stent System Lifestent and Lifestent XL Vascular Stent System Lifestent Solo Vascular Stent System

    Establishment Types

    Export Device to the United States But Perform No Other Operation on Device