We will explore the establishment of a management system for entrusted production of medical devices, optimize the allocation of resources, and implement principal responsibilities. Medical device registration applicants who apply for and obtain a medical device registration certificate shall become medical device registrants. The applicant may entrust an enterprise with the corresponding production capacity to produce the sample, and the registrant may entrust one or more enterprises with the production capacity to produce the product. Group companies are encouraged to further integrate and optimize resource allocation through the pilot registration system and implement the main responsibility of medical device registrants.