BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    LifeStar Vascular Stent System

    Reg #: 9681442 · FEI: 3002806368 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    2
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
    Registration Number
    9681442
    FEI Number
    3002806368
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    WACHHAUSSTRASSE 6
    City
    KARLSRUHE Baden-Wurttemberg
    Country
    DE

    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

    Manufacture Medical Device