BEUDAMED
    FDA Registration Active 🇺🇸 United States

    GlidePath™ 10F Long Term Dialysis Catheter

    Reg #: 2020394 · FEI: 2020394 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    BARD PERIPHERAL VASCULAR, INC.
    Registration Number
    2020394
    FEI Number
    2020394
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    Yes
    Address
    1625 W 3rd St
    City
    TEMPE
    State
    AZ
    ZIP
    85281
    Country
    US

    Regulatory Submissions

    510(k) Number
    K200627

    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

    GlidePath™ 10F Long Term Dialysis Catheter

    Establishment Types

    Manufacture Medical Device