BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Mini-Midline Extended Dwell Peripheral Catheter

    Reg #: 3017129766 · FEI: 3017129766 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    1
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    LUTHER NEEDLESAFE PRODUCTS LLC
    Registration Number
    3017129766
    FEI Number
    3017129766
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    26052 Merit Cir Ste 107
    City
    Laguna Hills
    State
    CA
    ZIP
    92653
    Country
    US

    Regulatory Submissions

    510(k) Number
    K130518

    Owner / Operator

    Firm Name
    Luther Needlesafe Products LLC
    Operator Number
    10087391
    Address
    26052 Merit Circle, Suite 107
    City
    Laguna Hills
    State
    CA
    Postal Code
    92653
    Country
    US
    Correspondent
    Amy Antonucci

    Products

    Device Name Product Code
    Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days FOZ

    Proprietary Names

    Mini-Midline Extended Dwell Peripheral Catheter

    Establishment Types

    Manufacture Medical Device