DomesticallyMedical EquipmentAgainst the backdrop of an industry with a market size exceeding trillion, medical equipment import general agents are transforming from traditional traders toSystem solution provider. High-quality general agents should possess:
Full-process hosting capability for registration and filing
CFDA registration certificate processing cycle shortened by 40%
Import license application approval rate increased to 92%
Customs clearance solutions for special items
Temperature control deviation handling plan for cold chain equipment
Special case for radioactive equipment transportation filing
Three key points for import qualification review in 2025
According to the latest working procedures of the National Medical Products Administration, special attention should be paid to the import of Class III medical devices:
Product classification matching degree: Verify product codes against the 2025 edition of the Medical Device Classification Catalog
Business license coverageCheck whether the agency scope includes special categories such as implantable devices
Customs AEO certification29. Inspection Rates for High-Level Certified Enterprises Can Be Reduced to 30% of the Standard Level
28. Four-Step Breakthrough Strategy in Customs Clearance Practice
27. To Address the Three Major Pain Points in Medical Equipment Customs Clearance (Timeliness, Compliance, Safety), a Step-by-Step Breakthrough Solution Is Recommended:
26. Precise Classification and Coding
25. Dual Verification of Medical Device Classification Directories and Customs HS Codes
24. Apply for Dedicated Customs Clearance Channels for Diagnostic Reagents