The timeline for processing NMPA (National Medical Products Administration) registration of medical devices in China can vary based on several factors, including the device classification, completeness of the submission, and the current workload of the NMPA.

Classification: Determine the correct classification of your medical device according to China's classification rules (Class I, II, or III). Classification is based on the device's intended use, potential risks to patients and users, and other factors.

Application Form: Complete and sign the application form provided by the NMPA.

Determine the classification of your medical device according to China's classification rules (Class I, II, or III). This classification determines the regulatory pathway and requirements.

Application Fees: The NMPA charges application fees for registration, which vary depending on the classification of the medical device. Fees can range from several thousand to tens of thousands of RMB (Chinese Yuan). Exact fees can be found on the NMPA's official fee schedule.

Classification and Risk Assessment: Determine the classification of your medical device according to China's classification rules. Classify the device based on its intended use, potential risks to patients, operators, and others, and the duration of contact with the human body.

Device Classification: Determine the classification of your medical device according to China's classification rules (Class I, II, or III). This classification will dictate the regulatory requirements and the specific registration pathway.

Classification of Your Device: Determine the classification of your medical device according to China's classification rules (Class I, II, or III). This classification will determine the applicable regulatory requirements.