FORYOU Medical's entire product line for the EU market has obtained MDR certification.

Great news! FORYOU Medical's entire product line for the EU market has obtained MDR (Medical Device Regulation) certification. This means our products not only comply with the latest EU medical device regulations but also can serve the European and global healthcare markets even better.

"Directive" becomes "Regulation": MDR carries more weight

The MDR, which was introduced by the EU in May 2017, is the latest medical device regulation, replacing the previous Medical Device Directive (MDD). Compared to MDD, the new MDR has stricter certification requirements, stronger regulatory oversight, and higher standards for products.

The primary aim of MDR is to enhance the safety and effectiveness of medical devices and ensure consistency across the EU market. It encompasses requirements from design and production through post-market surveillance.

FORYOU Medical's successful acquisition of this certification demonstrates that our products meet the EU’s stringent standards for quality and safety, fully attesting to Huayang Medical’s outstanding capabilities in technological innovation and quality management.

Gaining this MDR certification will open up more opportunities and expand our market share internationally. It also solidifies FORYOU Medical’s brand presence globally in the medical device sector, driving us towards new heights in our future development. We remain committed to developing innovative products and providing superior care solutions to contribute to global healthcare.

For you, for us, for life!