Which document you need and why

CU TR 010/2011 declaration and, where applicable, CU TR 032/2013 declaration or certificate

Industrial pipeline valves appear in the CU TR 010/2011 declaration list; CU TR 032/2013 applicability depends on pressure, diameter, medium and equipment category. Under 032, categories 1 and 2 generally require declaration and categories 3 and 4 certification, with special provisions for final manufacture on site. These documents cover identified products, but household taps, gas controls and industrial valves are not one regulatory category merely because they are all called valves.

What to send for a quotation

Start with these four items. If something is missing, send what you have and we will explain what else is needed.

01

Product name

Name, model, intended use and manufacturer.

02

HS / EAEU commodity code

Include the code if known. If not, we can help identify the product.

03

Technical description

Specifications, photographs, instructions or a product datasheet.

04

Composition and materials

Ingredients, materials or a component specification, depending on the product.

Provide maximum allowable pressure PS, nominal diameter DN, minimum and maximum temperature, and fluid identity and group. Include a body section drawing, main materials, actuator type, passport and welding information, and specify series, batch or single-unit supply.

Which requirements we check

  • Function and scope
  • Pressure and fluid category
  • Body strength
  • Seat and joint tightness
  • Materials and welded joints
  • Passport and PS/DN marking

How the process works

  1. 01

    Product

    Review the description and identify the required document.

  2. 02

    Assessment

    Check the records and arrange any required testing.

  3. 03

    Documentation

    Support the documentation and registration procedure.

  4. 04

    Your document pack

    Deliver the completed documents and agreed work results.

What you receive

  • Issued declaration or certificate for the specified valves after successful completion of the applicable procedure, or a written requirements assessment for products outside mandatory scope
  • Prescribed test reports
  • Reviewed passport and marking
  • Agreed technical file

Sources & regulatory basis

Timing & cost

Quoted after reviewing models, manufacturers, testing scope, site visits and translation needs. The proposal separates the stages and their deliverables.