European product conformity
What CE marking signifies
CE marking is used on products covered by applicable European Union legislation. It indicates that the manufacturer declares conformity with relevant requirements, after completing the required assessment procedure.
Which products require it
Applicability depends on the particular product and legislation. Examples can include certain medical devices, machinery, electrical equipment, toys and personal protective equipment. Requirements and conformity routes differ by product category.
Conformity route
The manufacturer identifies applicable requirements, collects evidence, prepares technical documentation and a declaration of conformity, and involves a notified body where legislation requires one. A private certificate alone is not a substitute for this process.
Astra-issued records
An Astra entry headed “CE” identifies an Astra-issued document under that label. It does not by itself establish lawful CE marking, notified-body involvement or access to the EU market.
Assessment areas
- Applicable EU legislation and product classification
- Technical documentation and conformity assessment
- Declaration of conformity and marking obligations
To check an Astra-issued record, use its certificate number in the public register.
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