European Union compliance · 04
CE is a manufacturer’s declaration—not a certificate issued by a central EU authority.
What to request when a power-adapter supplier says a product is CE certified: declaration, exact model, applicable rules and supporting technical evidence.
The short answer
There is no central EU body that issues permission or a universal “CE certificate.” For a product that requires CE marking, the manufacturer identifies the applicable EU rules, completes the required conformity assessment, prepares technical documentation, signs the EU Declaration of Conformity and affixes the mark. A buyer should therefore ask for the declaration and trace it to the exact product—not stop at a logo or voluntary certificate.
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Ask for the EU Declaration of Conformity for the exact model and manufacturer.
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Check listed legislation, standards, date, signatory and product identification.
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Treat a laboratory report or voluntary certificate as supporting evidence, not automatic legal permission to use CE.
Why “send me the CE certificate” is the wrong first question
The European Commission explains that CE marking is the manufacturer’s indication that the product meets applicable EU requirements. The manufacturer is responsible for the conformity assessment, technical file, declaration and mark. Some legislation permits self-assessment; some product routes require a notified body.
Because the route depends on the product, a document titled “Certificate of Compliance” can be relevant evidence but is not automatically the legal document that establishes the manufacturer’s declaration.
Read the Declaration of Conformity field by field
The declaration should identify the product and responsible manufacturer clearly enough to connect it to the item being purchased. It should list the applicable legislation and standards, and include the place, date, authorised signatory and statement of responsibility.
Power electronics may involve more than one applicable requirement depending on voltage, electromagnetic behaviour, radio function, materials and intended market. Do not copy a standard list from another product; compare the declaration with the actual architecture and ratings.
- Manufacturer and contact details
- Exact product, model and rating
- Applicable EU legislation
- Standards or specifications used
- Place, date, name, title and signature
- Notified-body details only when the applicable route requires one
Cross-check the supporting evidence
Compare test-report model names, ratings, photographs and construction details with the quotation and sample. Confirm that the issuing laboratory and report can be contacted or verified where possible. If a notified body number appears beside the CE mark, confirm that the body is authorised for the relevant legislation and procedure in the NANDO database.
The European Commission specifically warns about voluntary certificates that may be mistaken for legally recognised CE approval. The title of a document matters less than its legal role and connection to the exact model.
Buyer checklist
Buyer checklist
- Exact model and product rating
- Signed EU Declaration of Conformity
- Manufacturer identity
- Applicable legislation and standards
- Supporting reports matched to the same variant
- Notified-body scope when one is actually required
Official sources
Official sources
Facts in this note were checked against the following primary sources. Links open the source owner’s website.
- 01European Union — Your EuropeCE marking
- 02European CommissionCE marking — Internal Market, Industry, Entrepreneurship and SMEs
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