BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Soft-Cell Dual Lumen Catheter

    Reg #: 3006260740 · FEI: 3006260740 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    Bard Access Systems, Inc.
    Registration Number
    3006260740
    FEI Number
    3006260740
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    605 North 5600 West
    City
    Salt Lake City
    State
    UT
    ZIP
    84116
    Country
    US

    Regulatory Submissions

    510(k) Number
    K030277

    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, Hemodialysis, Implanted MSD

    Proprietary Names

    Soft-Cell Dual Lumen Catheter

    Establishment Types

    Complaint File Establishment per 21 CFR 820.198