Guidelines for Risk Control in the Entire Process of Medical Equipment Agency Importation
This article systematically analyzes the complete process of medical equipment import agency, with a focus on dissecting the clearance challenges of Class III medical devices. It provides operational guidelines for 12 key steps, including HS code verification, medical device regulatory filing, and cold chain transportation, along with the latest customs quarantine requirements and updates on the 2025 Medical Device Classification Catalog.
PSB Record: Shanghai No.31011502009912
