arcoro Glossar


The CE-marking identifies products that comply with the European policies on health and environmental protection, as well as product safety. The labeling is carried out by the manufacturer and must be clearly visible and permanently placed on the  medical device so that the conformity of the product with the applicable policies can be guaranteed. This administrative label enables the product to be placed on the market and to be used in the European Economic Area and Turkey.

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Anne Plonz

Business Analyst


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