BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    Bardex Double Pigtail Stent

    Reg #: 9681442 · FEI: 3002806368 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    7
    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

    510(k) Number
    K903345

    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, Ureteral FAD

    Proprietary Names

    Bardex Double Pigtail Stent Stent with Suture Bard Lubricious-Coated Ureteral Bard Fluoro-4 Silicone Ureteral Stent Bardex Double Pigtail Ureteral Stent with Suture Coil Stent Ureteral Coil Stent with Figure Four End

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer)