Which document you need and why
CU TR 019/2011: class 1 declaration or class 2 certification
The document addresses PPE safety and specified protective functions, with the route determined by risk class and product type. Non-protective uniforms, medical devices and specially designed firefighting equipment must not automatically be assessed under CU TR 019; exclusions and other regimes require review. Different protection claims on one glove or garment need corresponding evidence, so an unspecified “universal protection” label is not a substitute for intended-use details.
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.
Product name
Name, model, intended use and manufacturer.
HS / EAEU commodity code
Include the code if known. If not, we can help identify the product.
Technical description
Specifications, photographs, instructions or a product datasheet.
Composition and materials
Ingredients, materials or a component specification, depending on the product.
Specify body area, hazard, protection classes, sizes and service life. Provide layer construction, wearing/care instructions, PPE compatibility, storage, label photographs and previous tests; respiratory equipment also needs filter type and use conditions.
Which requirements we check
- Product type and risk class
- Evidence for protection claims
- Body-contact material safety
- Strength, fit and ergonomics
- Component compatibility and protection after care
- Marking, limits and clear instructions
How the process works
- 01
Product
Review the description and identify the required document.
- 02
Assessment
Check the records and arrange any required testing.
- 03
Documentation
Support the documentation and registration procedure.
- 04
Your document pack
Deliver the completed documents and agreed work results.
What you receive
- Competent-body certificate or registered declaration after successful assessment
- Included protection test reports
- Model and size evidence
- Corrected protection, limitation and care information within scope
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.