CE Marking - Polmed.de - EC Authorized Representative

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CE Marking

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The European Union decided to make the unification of standards of production and quality of the products throughout the EU. As a consequence, standards on ISO 9001 and ISO 13485 quality management, as well as evaluation criteria in the form of the unified procedures are entered in all territory of the European Union.

CE marking on a product:

Indicates to governments that the product can be legally sold within the European Union (EU) and the European Free Trade Area (EFTA)
Ensures the product can move freely throughout the European Single Market
Indicates to customers that the product meets designated minimum safety standards and therefore a minimum level of quality
Enhances product credibility
Leads to improved sales and greater customer satisfaction

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important notice

Polmed.de as the Authorized European Representative, can provide you with total support for complying with the CE marking for products sold in the EU market.

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