Center for Quality, Faculty of Engineering, University of Kragujevac, Serbia
Abstract
This research is part of Tempus ETIQUM Project which is financed by EU. This article covers the analyse of steps which were necessa ry for transposition and implementation of EU Directi ve on medical devices into the national legislation of the Slovak republic. It covers not only information about implementation but also mandatory periodic verification after placing the medical device with measuring function on the market as well