Class I production registration certificate: Is issued by the drug regulatory department, with legal production qualifications, safe and reliable products, demonstrating the company's professional strength and compliance guarantee。

Class II production and operation certificate: The Class II medical device production certificate is issued by the State Food and Drug Administration. It has legal qualifications and strictly follows industry standards to ensure product safety, effectiveness and compliance.。

ISO system certificate: Our company has passed ISO 13485 medical device quality management system certification, which complies with international standards, ensures compliance and safety throughout the product life cycle, and reflects professional quality and continuous improvement capabilities.。

CE certification: Our company has obtained the EU CE certification, which indicates that the product complies with the strict safety, performance and quality requirements of the EU medical device regulations (such as MDR or MDD), and can be legally marketed and sold in the European Economic Area。CE certification is reviewed and issued by a notified body authorized by the European Union. It is an internationally recognized authoritative mark for medical device access. It represents that enterprises have reached high standards in design and development, production management, risk control and clinical compliance.。This certification not only demonstrates our company's firm commitment to product quality and user safety, but also reflects the company's global vision and international competitiveness to provide customers with trustworthy medical solutions.。