CE marking shows that a product meets EU health, safety and environmental requirements and is mandatory for many product categories sold in the European Economic Area. The manufacturer identifies applicable EU directives or regulations, completes the conformity assessment (self-declaration or through a notified body), prepares a technical file, signs an EU Declaration of Conformity and affixes the CE mark.
Products that need CE marking
- Machinery and electrical equipment
- Medical devices
- Toys and personal protective equipment
- Radio equipment and electronics
- Construction products
Conformity assessment
- Identify applicable directives and harmonised standards.
- Determine if a notified body is required.
- Test the product against standards.
- Prepare the technical file.
- Sign the EU Declaration of Conformity and affix CE.
Role of the EU representative
Non-EU manufacturers often need an EU importer or authorised representative who keeps documents available to authorities and is identified on the product or packaging.
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Get expert help →Common pitfalls
- Missing applicable directives
- Incomplete technical files
- Using unaccredited test reports
Frequently asked questions
Is CE certification issued by a government?
CE marking is mainly a manufacturer's declaration. For higher-risk products, an EU notified body assesses conformity, but there is no single CE certificate issued by a government.
Does CE marking allow sale in the UK?
The UK uses UKCA marking in Great Britain, though CE marking has been accepted for many products for an extended period. Check current UK rules for your product.
How long does CE marking take?
It depends on the product and whether a notified body is involved. Simple self-declaration products take weeks, while medical devices can take much longer.
Can Indian manufacturers self-declare CE?
Yes, for product categories where self-declaration is allowed, provided testing and documentation meet the requirements.
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