1, Medical Device Registration Certificate: This is the certificate that the product meets the national medical device standards and has been registered. The certificate was issued by National Medical Products Administration, which clearly stipulated the technical requirements, production conditions, inspection methods, quality indicators and other information of the product.
2. Production license: this is a document that proves that the enterprise has the qualifications and conditions to produce a certain product. This certificate was issued by the General Administration of Quality Supervision, Inspection and Quarantine, and stipulated the requirements of production conditions, equipment, technological process and quality management system of the enterprise.