Which document you need and why

CU TR 004/020 certificate or declaration; EAEU TR 037 declaration for listed products

Documents address applicable electrical safety, EMC and hazardous-substance requirements. CU TR 004 has a defined voltage range, CU TR 020 concerns interference and immunity, and EAEU TR 037 covers its own product list; the three do not automatically cover every wired device. The certificate/declaration route depends on the exact category, with embedded components, high-voltage and special equipment assessed separately.

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 circuit diagrams, ratings, intended use, protection class, environment and key components. Identify power sources, enclosure options, programmable functions and accessories, with rating-label photographs, instructions, model differences and batch size.

Which requirements we check

  • Intended use and required documents
  • Insulation, earthing and user protection
  • Heating and current rating
  • EMC configurations and modes
  • Hazardous-substance evidence
  • Consistency of model, circuit, label and 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

  • Applicable documents after successful assessment
  • Agreed test reports
  • Model-specific evidence package
  • Label and instruction corrections needed to complete the procedure

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.