BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Inlay Ureteral Stent with Hydroglid

    Reg #: 3006082230 · FEI: 3006082230 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    C.R. BARD, INC.
    Registration Number
    3006082230
    FEI Number
    3006082230
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1211 MARY MAGNAN BLVD.
    City
    MADISON
    State
    GA
    ZIP
    30650
    Country
    US

    Regulatory Submissions

    510(k) Number
    K983498

    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

    Inlay Ureteral Stent with Hydroglid Inlay Uteral Stent Inlay VersaFit Multilength Ureteral Inlay VersaFit Ureteral Stent

    Establishment Types

    Sterilize Medical Device for Another Party (Contract Sterilizer)