Which document you need and why

Certificate or declaration for covered equipment; separate battery assessment

There is no single mandatory document covering every battery: requirements must be identified for the particular source and supplied configuration. EAEU TR 037/2016 expressly excludes batteries and accumulators, while a separate charger is assessed against the relevant scopes of CU TR 004/2011, 020/2011 and EAEU TR 037/2016. Lithium battery transport documents are considered separately and do not replace required equipment conformity assessment.

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 chemistry, nominal and maximum voltage, capacity in Ah and energy in Wh, and details of BMS, charger and inverter. Include the pack diagram, application, charging parameters, cell model, existing test reports and planned transport mode.

Which requirements we check

  • Battery versus complete-device identification
  • Voltage range
  • Overload and short-circuit protection
  • Battery–charger compatibility
  • Applicability of electronics requirements
  • Warnings and storage conditions

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 certificate or declaration for the relevant product after successful completion of the applicable procedure, or a written requirements assessment for products outside mandatory scope
  • Document list and regulatory basis for the supplied configuration
  • Test reports under the selected procedure
  • Agreed instruction and marking review

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.