SFDA Registration

On the base of potential risk and intended use, medical devices are divided into three management categories by SFDA ( State Food and Drug Administration) . All medical devices need to be registered according to Medical Device Registration Administration in order to be sold and used in China.
Different countries have different regulations about medical devices, relying on the deep understanding of various regulations and wealth practical experience, Osmunda could help your product to be approved by SFDA and introduced into Chinese market.