Latest 2025 customs data shows that ChinasMedical Equipmentimport volume is expected to exceed $28 billion, with three categories of medical devices accounting for 47%. Compared with ordinary goods, medical equipment imports involvea dual regulatory system: compliance with both the General Administration of Customs Supervisory Measures for the Inspection of Imported Medical Devices and the National Medical Products Administrations device registration requirements. In 2024, an MRI equipment purchase by a tertiary hospital was detained at port for 37 days due to incomplete agency qualifications, resulting in direct losses exceeding 800,000 yuan.
Professional agency companies should possessEnd-to-end process node control capability:
High-quality agency companies typically possessDual negotiation capability:
The newly implemented Medical Device Use Quality Supervision and Management Measures in 2025 require importers to provide:
Under the background of medical device import filing system reform in 2025, selecting anFull - chain service capabilitiesagency company can not only ensure compliant equipment entry but also shorten the procurement cycle by over 30% through professional services. It is recommended that enterprises require the agency to provide import cases of similar equipment in the past three years and conduct on-site inspections of their warehousing conditions and emergency handling capabilities when making selections.
? 2025. All Rights Reserved. Shanghai ICP No. 2023007705-2 PSB Record: Shanghai No.31011502009912