This article systematically analyzes the difficulties in equipment import declaration, compares the differences between professional agents and self-declaration, provides a four-dimensional evaluation system for qualification review, and includes a practical guide for medical device import clearance cases in 2025.
This article analyzes the key points of the latest medical device import policies for 2025, examines three types of special customs clearance risks, and provides selection criteria for agency services to help enterprises avoid customs clearance delays and compliance risks.
This article analyzes the selection criteria for professional equipment import customs clearance agents from three core aspects: commodity classification, document pre-review, and risk warning, incorporating the latest 2025 policy changes. Through practical case comparisons, it reveals essential differences in special regulated materials handling capabilities among different service providers.
This article details the key points of the 2025 tax exemption policy for imported equipment, including applicable conditions, application procedures, common misunderstandings, and advantages of agency services, helping enterprises legally enjoy tax benefits and reduce equipment introduction costs.
This article analyzes the 7 key processes and 3 core advantages of medical device imports through the case study of ZhongShen International Trade's X-ray diffractometer import agency, providing professional reference for scientific equipment imports.
This article provides an in-depth analysis of the entire import process for rehabilitation physiotherapy equipment, focusing on three core aspects: qualification certification, customs clearance strategies, and cost control. Through real case studies, it reveals the value of professional agency services in risk avoidance for medical device imports.
This article analyzes three major technical thresholds for hydrogen-rich equipment imports, compares cost differences between self-operation and professional agencies, and reveals the key roles of compliant declaration, certification coordination, and logistics optimization through practical cases.
This article analyzes 9 core steps in the medical equipment import process, highlighting key operational points in registration filing, customs classification, and quality traceability, while providing a 4-dimensional evaluation system for selecting professional agency service providers.
This article provides an in-depth analysis of the three core aspects of instrument equipment imports, from qualification verification to clearance solution design, combined with the latest policy changes in 2025, offering a practical guide for enterprises to choose import agents and avoid typical risks.
? 2025. All Rights Reserved. Shanghai ICP No. 2023007705-2 
PSB Record: Shanghai No.31011502009912
