Medical EquipmentChanges in import regulations

2025 General Administration of Customs policies on medicalEquipment ImportsimplementationDynamic classification management, reclassifying 3,217 tariff code equipment into three regulatory tiers. Among these, Class II and Class III medical devices require simultaneous submission ofMedical Products Administration registration and filing certificatesandQuality certification documents from the country of origincomparison statements during customs clearance. This new regulation has already resulted in 13.7% of declarations being rejected in Q1 due to document mismatches.

Key control points in the customs clearance process

• Qualification pre-review stage
  • Verify whether the equipment is listed in the 2025 edition of Medical Device Classification Catalog
  • Cross-check HS codes with corresponding regulatory certificates
• Declaration link
  • New equipment requires advance application for commodity pre-classification
  • Implantable devices must include a biocompatibility report
• Inspection Phase
  • Radioactive equipment requires a radiation safety license
  • Diagnostic reagents cold chain transportation temperature record verification

Core value analysis of agency services

The value of professional customs clearance agents lies not only in document processing speed, but also in:

• EstablishMedical device databaseReal-time tracking of standard updates in 42 major global markets
• Equipped withPre-classification expert teamHandling complex equipment classification disputes
• Set upEmergency declaration channelAddressing delays in data synchronization between drug regulatory authorities and customs

Typical case warnings for 2025

A provincial hospital importing a digital subtraction angiography system experienced a 47-day port detention of equipment worth 120 million yuan due to the agencys failure to promptly obtain the EUs new MDR certificate conversion information. Professional agencies can avoid such losses through the following mechanisms:

• Establishing a dual certificate validity verification system
• Implementing a 60-day document expiration warning mechanism
• Deploying a multilingual certification document translation verification team

Agency selection evaluation model

• Basic competency items
  • China Customs Brokers Association AAA-level qualification
  • Quantity of medical device import case database
• Value-added Service Items
  • Global standard differential comparison system
  • Emergency guarantee release quota

With the implementation of the revised version of the Medical Device Supervision and Administration Regulations in 2025,Import Clearancehas been upgraded from a simple logistics link toThe EUs new Battery Law (2023) requires importers to provide a carbon footprint statementa battle of offense and defense. Choosing professional customs clearance agents with medical expertise will become a key decision for enterprises to control import costs and ensure supply chain stability.