Beijing Tigermed-Jyton Co., LTD. ——China NMPA Registration Services

Medical devices, which are / will be marketed and used in the People’s Republic of China, shall be registered / filed with the NMPA / local authorities. We can recommend the product registration path for companies, formulate the most reasonable marketing strategy, give warning to possible risk points in advance, and provide reasonable suggestions for risk avoidance to improve the efficiency and to increase success rate of product approval. We can provide you with the proper services regardless of the status of the product. Our services include but not limited to: 1. Product Classification Application / Attribute Application 2. Class I device filing / change filing 3. Class II / III device initial registration 4. Class II / III device renewal registration 5. Change filing of Class II / III device 6. Change registration of Class II / III device 7. Clinical trial application 8. Intent for Use (IFU) changes 9. Medical device certificate re-issuance / error correction / cancellation 10. Other green channel applications, such as innovation application, priority review, emergency use approval, etc