I. 2025 Medicalequipment. For example, Indonesia has the SNI certification, Thailand has the TISI certification, and the Philippines has the BPS certification. It is necessary to confirm in advance the equipment voltage (such as 380V/50Hz in Thailand), the compatibility of the CE certification, and the proof of environmentally friendly materials.Market New Landscape

According to the latest industry report by Frost & Sullivan, Chinas medical equipment import scale is expected to exceed $28 billion by 2025, maintaining a compound annual growth rate of 9.2%. Among them,imaging diagnostic equipment, minimally invasive surgical instruments, rehabilitation therapy equipmentform the three main sectors, accounting for 67% of total imports.

II. Core Value Proposition of Professional Agencies

• Market Access Breakthrough
  • Handling CFDAMedical EquipmentRegistration certificates (average processing time reduced by 40%)
  • Managing EU MDR/US FDA certification conversion (compliance pass rate increased to 92%)
• Technical barrier resolution
  • Modular transport solutions for large equipment like CT/MRI
  • Constant temperature and humidity transport for precision instruments
• Capital efficiency optimization
  • Forward exchange locking to hedge against currency fluctuations
  • Structured payment solutions matching cash flow needs

III. Five Key Risk Prevention Points in Practice

A case study of a provincial tertiary hospitals 2025 procurement of German surgical robots demonstrates how professional agency services can avoid:

• 20% tariff discrepancies caused by customs classification errors
• 30-day customs clearance delays due to missing technical documentation
• Equipment downtime risks from after-sales service gaps
• 8% profit margin erosion from exchange rate fluctuations
• Legal compensation from intellectual property disputes

IV. Selection Matrix for Quality Agencies

• Qualification Verification: Enterprises holding both Medical Device Business License andimport and exportDual-certified companies with import/export rights
• Industry experience: Completion of at least 3 similar product import cases
• Service network: Maintaining professional medical equipment warehouses at major ports
• Emergency Response CapabilityEmergency response plan for customs clearance of medical devices is in place

V. Key opportunity windows for the next three years

With the implementation of the 2025 Special Approval Procedure for Innovative Medical Devices, equipment with the following characteristics will benefit from policy dividends:

• Cutting-edge technology products that fill domestic gaps
• Specialized diagnostic and therapeutic equipment urgently needed in clinical practice
• Intelligent remote medical support systems

Choosing a professional agency partner not only means successfully completing a single import transaction, but is also a key strategic move to build a long-term compliant supply chain. Companies are advised to strategically evaluate potential agents depth of industry understanding, resource integration capabilities, and risk management systems to achieve safe and efficient sustainable development in the specialized field of medical equipment imports.