* No CONTEMPLAS GmbH product is classified as a medical device under MDR (EU) 2017/745 within the European Union, United Kingdom (excluding Northern Ireland) under Part II, UK MDR 2002 (SI 2002 no. 618) or within the requirements of any other national medical regulatory body. CONTEMPLAS GmbH supplied products must not be used where the intention is to provide information which will be used to take decisions with diagnosis or therapeutic purposes.