This article deeply analyzes the core difficulties in the customs clearance of imported instruments and equipment in 2025. From the particularity of HS code classification to the new regulations for medical device filing, combined with practical cases, it reveals the six key service capabilities of professional customs declaration agents, helping enterprises avoid the risk of port congestion.
This article analyzes the core legal elements of the agency authorization letter for importing medical equipment, focuses on analyzing the changes in document signing brought about by the latest regulatory adjustments in 2025, reveals the common legal risk points of cross - border authorization documents, and provides professional suggestions for choosing foreign trade agents.
This article provides an in-depth analysis of the latest regulatory requirements for pharmaceutical equipment imports in 2025, revealing three major compliance risks in medical device classification, technical standard certification, and certificate of origin, while offering selection criteria for professional customs brokers and comprehensive operational guidelines.