On May 18th, May 18, the State Food and Drug Administration issued public information, and another batch of medical device industry standards will be formulated and revised, involving a total of 99.
Notice that according to the relevant Regulation The request, the Bureau organizes the launch of 2018 medical instruments industry standard Selection and revision of project selection, public opinion solicitation, and organization of expert demonstrations, identified 99 items of the medical device industry standard revision plan in 2018, and publicized it.
The following is the 2018 medical device industry standard revision plan project:
