Clinical excellence

All our devices follow Directive 93/42/EEC revised 2007/47/EEC and meet the requirements of French and international standards. They are subject to individual rigorous unit tests in our laboratories. The labelling procedure of our devices follows a quality system which is ISO 9001:2008 and ISO 13485 Version 2003.
The safety of our employees as well as patients safety are our first priority. The new standards and regulations, as well as good clinical practices which aim at preventing infection and providing a greater efficiency in the operating room, are central to the development of our devices.