What are the different types of EU directives relevant to CE marking?

Directive 2014/68/EU defines the safety requirements for pressure equipment throughout the EU and the European Economic Area. The letters "CE" are the abbreviation of French phrase "Conformité Européene" which literally means "European Conformity". The term initially used was "EC Mark" ... CE marking does not mean that a product was made in the EEA , but shows that the product meets all the relevant EU requirements and has been assessed as such ... 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 checklist for CE marking shows which steps you need to take to get a CE marking for your product. Nov 1, 2014 ... The added value of CE marking is that all EU countries must allow the selling of construction products bearing the CE mark. This means that ... CE marking of bituminous mixtures is based on a 2+ assessment system, applying the EN 13108 family of standards. Manufacturers can place a CE (Conformité Européenne) mark on a medical device once it has passed a conformity assessment. The conformity assessment usually ... We are regulatory professionals who guide on specific requirements that must be met and obtain the medical device CE Marking. CE-marking services from SGS – meet the compulsory product safety directives you need to trade in the EU with effective conformity assessment services.