CE MARKING AND CONFORMITY
The CE marking is a significant indicator that the product complies with European legislation and allows the free movement of products within the European market. When a manufacturer affixes the CE marking to a product, he declares, under his sole responsibility, compliance with all the legal requirements necessary to affix the Medical Device CE Marking , and thus gives rise to the product being able to be sold in the space European economy, Switzerland and Turkey. This also applies to products made in third countries that are sold in the European Economic Area (EEA), Switzerland and Turkey. The CE marking does not indicate that the product has been manufactured in the EEA, but rather that the product is evaluated before being placed on the market and meets the Union's safety, health and environmental protection requirements. This means that the manufacturer verifies that the product meets all the essential requirements of the Directives that apply to it or, if stipulated in the D