Telic Group, a manufacturing company of disposable solutions for the healthcare sector, has completed the certification of its products under the new European Medical Device Regulation 2017 / 745 (MDR – Medical Device Regulation).

With MDR certification, Telic becomes one of the few companies in the sector to complete the adaptation process. At the present, only 8% of the product certificates issued under the old MDD Directive have been transferred to the new Regulation that ensures their long-term market presence.


The European Medical Device Regulation 2017/745 MDR, which replaced the MDD 93/42/EEC Medical Device Directive, entered into force on May 25, 2017. Although the European Commission has proposed several transitional periods, before May 26, 2024, all manufacturers must have completed and submitted the documentation for the MDR conformity assessment. Otherwise, the continuity in the market for these products will be compromised.

Therefore, Telic ensures the availability of its products in the European market, indirectly guaranteeing the continuity of healthcare activity, which can be seriously affected by delays in the certification of medical devices.

Telic's medical division has been providing single-use medical consumables for the areas of surgery, cardiology, nursing care and patient wellness for over 40 years. The high-quality standards of its products have led the company to have the confidence of the sector in more than 100 countries around the world.