BEUDAMED
    FDA Registration Active 🇺🇸 United States

    4710 ¿ Bag Spigot with non-vented spike

    Reg #: 3020778 · FEI: 3020778 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    9
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    PROCEDURE PRODUCTS, INC.
    Registration Number
    3020778
    FEI Number
    3020778
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    1801 WEST 4TH PLAIN BLVD.
    City
    Vancouver
    State
    WA
    ZIP
    98660
    Country
    US

    Regulatory Submissions

    510(k) Number
    K910673

    Owner / Operator

    Firm Name
    Procedure Products, Inc.
    Operator Number
    3020778
    Address
    1801 WEST 4TH PLAIN BLVD., --
    City
    Vancouver
    State
    WA
    Postal Code
    98660
    Country
    US
    Correspondent
    Eric - Dietz

    Products

    Device Name Product Code
    Container, I.V. KPE

    Proprietary Names

    4710 ¿ Bag Spigot with non-vented spike 4722 ¿ Spike with Female luer lock Bag Spigots ¿ I.V. Plumbing Adapters ¿ Sterile and Non-sterile 47-722 Universal Spike w/72¿ line 4771 - 3-way stopcock 4¿ tubing and spike 91-722 Univeral Macro Chamber w/ 72¿ line 4709 ¿ Bottle Spigot universal vented spike 4721 - Spike with Male Luer Lock 4770 - 1-way stopcock 4¿ tubing and spike

    Establishment Types

    Manufacture Medical Device