CE is a manufacturer's declaration that a product meets the necessary health, safety, and environmental requirements established in the relevant European product legislation and has undergone the relevant conformity assessment method is known as marking on a product.

CE mark is mandatory to sell products in European Economic Area (EEA).

The CE mark and EC Declaration of Conformity are valid as long as your product complies with the directive's applicable health, safety, and environmental standards (s). If the product (or component) undergoes changes in design or features, it may be necessary to test it to ensure that it remains compliant with the relevant directive. Furthermore, changes to the applicable legislation and/or harmonized standards may necessitate retesting the product to establish compliance.

Netherland, Bulgaria, Romania, Luxembourg, France, Germany, Italy, Ireland, Denmark, Greece, Spain, Portugal, Austria, Finland, Sweden, Cyprus, Estonia, Hungary, Latvia, Lithuania, Malta, Poland, Slovenia, Slovakia, Czech Republic.

The government of the relevant member state can take action if a product is marked with the CE label illegally. Products may be pulled from the market, and penalties may be applied. If the CE mark has been fixed unlawfully or if the product does not satisfy the standards stipulated by the EU harmonized standards, manufacturers, importers, and/or authorized representatives will be held accountable.

If a non-EU manufacturer makes the device, the person who commercializes it in the EU assumes all of the responsibilities that would normally fall on the manufacturer or their authorized representative and must ensure that the device meets the essential requirements and submit all relevant documentation for control purposes, if necessary. This system does not apply if created by an EU company, and liability cannot be transferred to a third party (distributor, user, etc.). When an authorized EU agent is involved, this is also true