Base on the potential risks and intended use, medical devices are divided into three management categories by SFDA of China (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 abundant practical experience, Osmunda could help your products to be easily approved by SFDA and be introduced into the Chinese market.
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