August 18, the State Council issued a "Drug and Medical Device review and approval system view" that the regulations issued by the State Council, highlighting the importance of the authority and its irreplaceable. Medical devices, the core of the four points:

One is to encourage innovation, particularly for approval;

Second, the revised standard, improve the domestic quality;

Third, adjust classification, the approval authority delegated;

Fourth, improve the registration fee, later adjusted once every five years to take care of small and micro enterprises.

In fact, these four points in the CFDA had more than a year, the vast majority have been carried out, implemented and push forward, but in the "registration fee adjusted once every five years, to take care of small and micro enterprises," originally did not seem to mention. So, after the file, the medical device industry will produce what kind of impact?