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Medical instrument registration certificate
Medical device registration refers to the process of systematically evaluating the safety and effectiveness of the medical devices to be marketed and used in accordance with legal procedures, so as to decide whether to agree to their sale and use.
Medical device production license
The medical device production license is a certificate that medical device manufacturing enterprises must hold, issued after review by the local drug administration. Establishing a medical device manufacturing enterprise should comply with the national medical device industry development plan and industrial policies.
Business license of medical devices
Certificates required for the operation of medical devices (instruments, equipment, instruments, materials or other articles used solely or in combination on the human body, including the required software).