Recently, Kossel’s independently developed Selethru® PTCA balloon dilatation catheter has successfully passed the EU Medical Device Regulation (MDR) certification, marking that the product has met the highest international standards in terms of safety, effectiveness and clinical performance.

Europe is a globally important medical device market. The acquisition of MDR certification has provided strong support for Kossel to continue its in-depth expansion into Europe and its affiliated markets. In the future, the company will continue to advance the “Local Base, Global Reach” overseas strategy, strengthen cooperation with global medical institutions and experts, and enable more patients to benefit from Chinese medical devices!