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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
医疗器械生产许可证是医疗器械生产企业必须持有的证件,由当地药监局审核颁发。开办医疗器械生产企业应当符合国家医疗器械行业发展规划和产业政策。
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).