BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Preconnected Bardex Lubricath Catheter (for Canada)

    Reg #: 1018233 · FEI: 1018233 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    Establishment Types
    2
    Classifications
    1

    Registration Details

    Registration Name
    C.R. BARD, INC.
    Registration Number
    1018233
    FEI Number
    1018233
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    8195 INDUSTRIAL BLVD.
    City
    COVINGTON
    State
    GA
    ZIP
    30014
    Country
    US

    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
    Catheter, Coude EZC

    Proprietary Names

    Preconnected Bardex Lubricath Catheter (for Canada) SureStep Foley Tray System Bard Lubricath Foley (for Canada) SureStep Foley Tray System Bardex Lubricath Coude Foley Catheter (for Canada) Bardex Lubricath Foley Catheter (for Canada) Bard Foley Tray with Bard HydrophilicCoated Foley Catheter (for Canada) Bard Urine Meter Foley Tray with Bardex Lubricath Foley Catheter (for Canada) Bard Urine Meter Bladder Care Tray with Bardex Lubricath Foley Catheter (for Canada) SureStep Foley Tray System (for Canada)

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer) Develop Specifications But Do Not Manufacture At This Facility