Are there any exceptions to the principle of mutual recognition?

Feb 8, 2022 ... Devices in the Class IIa category are for short-term use (30 days or less), such as tubing intended for drug delivery, syringes, and surgical ... 1. The CE marking shall be subject to the general principles set out in Article 30 of Regulation (EC) No 765/2008. CE marking is a process that applies to a wide variety of products and one which manufacturers located in the EU or importers of goods into the EU must ... Many products are covered by these directives and, to be placed on the European market, must bear the 'CE' mark - it's a legal requirement. CE marking is the ... Jul 28, 2022 ... Which medical devices require a CE mark? All medical devices sold in the EU require a CE mark. While a CE mark is not required for items such as ... CE marking is a mark that manufacturers use to indicate that a product meets relevant European Union (EU) legal conformity standards in terms of safety, health ... The "CE" marking is a European logo indicating that the manufacturer has complied with certain compliance requirements to which the product is subject, to put ... CE marking of bituminous mixtures is based on a 2+ assessment system, applying the EN 13108 family of standards. Sep 17, 2022 ... A CE marking cannot legally exist on its own, it has to be backed by a declaration of conformity which in turn has to be backed by appropriate ... Let us guide you through the principles of CE marking step by step. We explain many of the words used in the context of CE marking, and you can get answers to ...