This article systematically analyzes the special requirements for medical device imports, from qualification certification and customs clearance capabilities to risk control systems, providing quantifiable evaluation criteria for enterprises to choose professional agency companies. It focuses on analyzing the impact of new 2025 medical device regulatory dynamics on import procedures.
This article uses the 2023 case of Japanese beauty device imports to explain the entire customs clearance process at Shanghai Airport and the core value of professional agencies, sharing practical experience in importing medical device products.
This article analyzes key points of agency-imported experimental equipment in 2025, covering three major customs clearance challenges: certification, tariff classification, and technical standards. It provides a professional agency service selection guide and combines it with the latest customs declaration system upgrade case to help companies avoid million-level compliance risks.
Must-read for foreign traders: The risk codes behind Sinosures Special Watch List,
This article analyzes three core pain points in hydrogen water equipment imports, compares practical customs declaration cases, reveals the key role of professional foreign trade agents in commodity classification, tariff optimization, testing and certification, and provides predictions on 2025 industry compliance trends.
This article provides in-depth analysis of three major profit growth points in equipment import agency business, revealing specific implementation strategies for tariff planning, currency hedging, and logistics optimization, with real case studies showing how different operational models affect final profit margins.
Professional bidding agency services can shorten procurement cycles by 22 days, reduce dispute risks by 73%, and achieve 14-18% cost savings through a four-dimensional empowerment model including qualification verification and risk control. This article details medical device procurement case studies and agency selection criteria.
This article systematically analyzes key points for importing GE medical equipment through authorized German agents, including qualification certifications, customs clearance strategies, logistics solutions, and 2025 EU medical device regulatory updates, providing full-process solutions for medical equipment importers.
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PSB Record: Shanghai No.31011502009912
