EU updates guidance on device classification
This article was originally published in Clinica
Executive Summary
An updated version of the European Commission's guidelines on the classification of medical devices (Meddev 2.4/1) should be available by the end of the year, following a meeting of the expert working group in Brussels at the end of last month. Mika Reinikainen, who chaired the meeting, said the document will be revised for updating following the next meeting of the group in early December.