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fectiveness can be ensured through routine administration; Class II Medical Devices are those for which further control

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is required to ensure their safety and effectiveness Class II▓I Medical Devices are those which are implanted into the human body, or used for life support or sustenance, or pose potential risk to the human body and t

hus must be strictly controlled in respect to safety and effectiveness. The classification catalogue for medical devices shall be stipulated, adjusted and promulgated by▓ the drug regulatory authority under the St

  • ▓or a physiological process;4. Control of conception. Article 4 The drug regulatory authority under the State Council is responsible for supervision and
  • administrat▓ion of medical devices nationwide. The drug administrati▓on of the local government at county level and above is responsible for supervision and administration
ade a turnaround, and we made major new achievements in reform and opening u Duis in tincidunt lorem. Nunc et tellus nisi. Nulla non velit lectus. Morbi luctus ullamcorper felis, non gravida neque congue sit amet. Nam nec mi metus, ac elementum velit. Etiam vel arcu velit, eget consequat risus.
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OCT 29, 2024

ate Council, in accordance with classificati▓on principles after consulting w

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OCT 28, 2024

ith health authorit▓y under the State Council. Article 6 Medical devices produced

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OCT 27, 2024

and used for the p▓urpose of providing concrete measuring values

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