BEUDAMED
    FDA Registration Active 🇧🇪 Belgium

    LifeStar Vascular Stent System

    Reg #: 3002504068 · FEI: 3002504068 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    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
    P080007

    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, Iliac NIO

    Proprietary Names

    LifeStar Vascular Stent System E-Luminexx Vascular Stent System

    Establishment Types

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