Ministru kabineta 2017. gada 28. novembra noteikumi Nr. 689 "Medicīnisko ierīču reģistrācijas, atbilstības novērtēšanas, izplatīšanas, ekspluatācijas un tehniskās uzraudzības kārtība".

This procedure establishes the rules for registering, assessing conformity, distributing, operating, and technically supervising medical devices. It aims to ensure the safety and effectiveness of these products available on the market. These regulations affect manufacturers, distributors, and users of medical devices, outlining their responsibilities and the requirements for compliance with national and EU standards.