Medical Equipment
Agent Import of Class I and Class II Medical Devices
How can medical device import agents avoid hidden risks?
This article deeply analyzes the key points of the whole - process operation of medical device imports, disassembles the whole chain from qualification review to customs clearance and inspection, focuses on expounding the three core risk areas of product registration, quality certification, and customs classification, and provides a methodology for choosing foreign trade agency services and risk prevention and control strategies.
PSB Record: Shanghai No.31011502009912
