BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Polyurethane Lines, Braided Lines, Injector Lines, Pressure Monitoring Lines

    Reg #: 3020778 · FEI: 3020778 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    7
    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
    K914128

    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

    Polyurethane Lines, Braided Lines, Injector Lines, Pressure Monitoring Lines Male/Female, Female/Female, Male/Male Configurations 1200 PSI, 1000 PSI, 500 PSI and below 10¿, 12¿, 15¿, 20¿ 24¿, 30¿, 36¿, 48¿, 60¿ and 72¿ Lengths Roentgenography Sets and/or Connecting Sets Sizes: OD .110, .140, .155, .187 and .215 Fixed and Rotator ends High Pressure, Standard Pressure Lines

    Establishment Types

    Manufacture Medical Device