It covers the design, classification, production, market supply, service and inspection of medical devices and medical medicine secession sparked by the use of these devices and accessories to protect patients, practitioners, users and third parties from the dangers that may arise in terms of health and safety. (CE Program – Medical Devices Directive EEC/93/42)
It should carry out the hygienic adequacy of production facilities and devices, microbiological tests on products before and after sterilization, and scanning pollutants that can fall behind the sterilization process (Endotoxins, Ethylene Oxide).
We provide testing services to test the suitability of the product according to the specified criteria so that medical devices can be declared that they meet the mandatory requirements of medical device regulations.
Our Other Analysis and Services