BEUDAMED
    FDA Registration Active 🇺🇸 United States

    4502 - Waste Bag System with Dual Check Valve Bonded

    Reg #: 3020778 · FEI: 3020778 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    8
    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
    K874037

    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
    Catheter, Intravascular, Diagnostic DQO

    Proprietary Names

    4502 - Waste Bag System with Dual Check Valve Bonded Waste Bag Systems ¿ Sterile and Non-Sterile 4803 ¿ 1000cc/ml or above waste bag with female lock 4571 ¿ Waste Bag System and Stopcock with Dual Check Valve ¿ Bonded/Attachable 4801 ¿ 1000cc/ml or above waste bag w/ male lock 4512 ¿ Waste Bag System with Dual Check Vale and Macro Drip ¿ Bonded or Attachable 4822 ¿ Waste Bag with dual Check valve and 10¿ line ¿ Bonded or Attachable 4559 ¿ Waste Bag System with Dual Check Valve Attachable

    Establishment Types

    Manufacture Medical Device