Which document you need and why

CU TR 032 declaration or certificate according to category and manufacturing method

Equipment in categories 1 and 2 generally requires a declaration, while equipment in categories 3 and 4 requires certification. Special cases, including permanent joining at the operating site, require separate review; product conformity documents do not replace hazardous-facility operating requirements. A certification body issues the certificate, while the applicant adopts the declaration; PLANCK helps prepare the documents and arrange the required checks.

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 design and maximum allowable parameters, each chamber’s volume, piping diameter, fluid properties and group, drawings, strength calculations, welding details and final assembly location.

Which requirements we check

  • Correct category and scope exclusions
  • Strength calculations for shell and joints
  • Material and welding-record traceability
  • Leak tightness and prescribed pressure tests
  • Safety devices and allowable conditions
  • Passport, markings and safe operating instructions

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

  • A certificate or registered declaration for the agreed products, where the selected procedure requires it and assessment is successful
  • A test report where testing is required by the procedure and included in the agreed work
  • Reviewed passport, instructions or label artwork within the agreed scope
  • An applicant’s file identifying products, conditions of use and any limitations found

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.