We did it!
We received the MDR certificate from our notified body TüV Süd according to the new EU Medical Device Regulation 2017/745.
This certificate covers as first product group the cylinder pressure regulators of class IIb. At the same time, we also successfully recertified our quality management system for medical devices in accordance with EN ISO 13485 by Tüv Süd.
![[Translate to English:]](/fileadmin/_processed_/1/c/csm_ad_jetflow80_03eb25e53b.jpg "Flow controller SWISS optio jetflow for high flow oxygen therapy")
