BEUDAMED
    FDA Registration Active 🇩🇪 Germany

    ANGIOMED GMBH & CO. MEDIZINTECHNIK KG

    Reg #: 9681442 · FEI: 3002806368 · Expires 2026
    View on FDA
    Products
    7
    Proprietary Names
    21
    Establishment Types
    3
    Classifications
    7

    Registration Details

    Registration Name
    ANGIOMED GMBH & CO. MEDIZINTECHNIK KG
    Registration Number
    9681442
    FEI Number
    3002806368
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    WACHHAUSSTRASSE 6
    City
    KARLSRUHE Baden-Wurttemberg
    Country
    DE

    Regulatory Submissions

    510(k) Number
    K053404
    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
    Stents, Drains And Dilators For The Biliary Ducts FGE
    Stent, Superficial Femoral Artery NIP
    Stent, Ureteral FAD
    System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis Treatment PFV
    Dislodger, Stone, Basket, Ureteral, Metal FFL
    Stent, Iliac NIO
    Stent, Iliac Vein QAN

    Proprietary Names

    LifeStent XL Biliary Stent System LifeStent Biliary Stent System LifeStent 5F Vascular Stent System Lifestent Solo Vascular Stent System Lifestent and Lifestent XL Vascular Stent System Bardex Double Pigtail Stent Bard Lubricious-Coated Ureteral Stent with Suture Coil Stent Bardex Double Pigtail Ureteral Stent with Suture Bard Fluoro-4 Silicone Ureteral Stent Ureteral Coil Stent with Figure Four End Covera Vascular Covered Stent Fluency Plus Endovascular Stent Graft Lifestent XL Biliary Stent System E-Luminexx Vascular Stent System LifeStar Vascular Stent System Venovo Venous Stent System LifeStar Biliary Stent System E-LUMINEXX Biliary Stent System FLEXXUS Endoscopic Biliary Stent

    Establishment Types

    Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) Complaint File Establishment per 21 CFR 820.198