Health technologies defined broadly embrace a range of applications of organized knowledge and skills in the form of pharmaceuticals, medical devices, vaccines, medical and surgical procedures, and systems developed to improve health. Within this broad definition, medical devices include a wide-ranging and heterogeneous group of health technologies that are used to diagnose illness, to monitor treatments, to treat acute and chronic illnesses, and to assist disabled people. The European Union (EU) market has over 500,000 types of medical devices. With an estimated market size of roughly €100 billion, medical devices account for about 7.5% of healthcare expenditure in most publicly funded healthcare systems. These technologies are indispensable tools for quality health care delivery, but their assessment and appropriate use pose significant challenges to policy makers. The challenge is to adopt policies to allow access to safe and effective technologies while providing adequate incentives to the industry to invest in research and development of new products.In the effort to properly address these challenges and overcome the gaps of the past, policy makers in Europe have for years discussed new rules for licensing and market access of medical devices in the EU market. These long discussions resulted in