What is CE Mark?
The CE mark shows that a product meets EU health, safety and environmental requirements. It is mandatory for many product categories, such as machinery, electrical equipment, toys and medical devices sold in Europe.
Depending on the product, CE marking is done by self-declaration or through an EU Notified Body.
Who Needs CE Mark?
- Exporters of machinery, electronics and medical devices to Europe
Advantages of CE Mark
EU market access
Sell legally across the EEA.
Product safety
Demonstrates compliance.
Documents Required for CE Mark
Product
- Product specifications and drawings
- Test reports
- Risk assessment
- User manual
We share an exact checklist for your case after the consultation. Scanned copies or clear phone photos are fine.
How We Get It Done
- 1Directive mapping
Applicable EU directives identified.
- 2Testing
Product tested.
- 3Technical file
Documentation prepared.
- 4Declaration
Declaration of conformity and marking.
Estimated timeline15–45 working days
Frequently Asked Questions
It is recognised in the EEA and Turkey. The UK now uses UKCA marking for most products.