SUNNYCO is categorized under Class III sterile medical device manufacturers. Our production cleanrooms are constructed in strict adherence to GMP standards to ensure product quality meets regulatory requirements. We incorporate imported high-precision manufacturing equipment and materials that comply with FDA standards, utilizing international production technologies and manufacturing processes. Quality management is rigorously conducted in accordance with both ISO13485 and GMP standards and system documentation, ensuring quality supervision from the procurement of raw materials to the approval of finished products. Through the implementation of "6S" onsite management, we ensure the stability of the production process, thereby guaranteeing and enhancing product quality. This approach underpins our commitment to the legalization, scientification, and standardization of company management.