Agent Import of Class I and Class II Medical Devices
This article details the foreign trade process for importing electronic blood pressure monitors from Japan, focusing on document processing, logistics arrangements, and trade situation analysis, providing professional guidance for importers to help them successfully conduct business.
This article analyzes six key aspects of medical equipment import customs clearance, revealing the core value of professional agency services in qualification review, tariff optimization, and emergency handling through real cases, while providing agency selection strategies for enterprises of different scales.
This article focuses on importing high-end medical devices from Germany, detailing key points in foreign trade import/export, including documentation and logistics processing, procedures for different markets, and certification assistance, while analyzing trade conditions and opportunities.
This article provides an in-depth analysis of the new 2025 medical equipment import declaration regulations, covering medical device classification management to customs clearance documentation requirements. Through typical cases, it reveals the crucial role of professional agents in handling technical reviews, import license applications, and other key processes, offering practical suggestions for enterprises to avoid compliance risks.
Troubles in beer import clearance? These details may cost you everything
This article analyzes the three core principles for medical device companies to achieve red light equipment import without deposit under the latest 2025 import policy through professional agents, compares the capital occupation differences with traditional models, and provides a five-step qualification review method and risk prevention plan.
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.
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PSB Record: Shanghai No.31011502009912
