15. In September 2022, a batch of RF beauty devices from Japan landed at Shanghai Pudong International Airport. As professionalsImport Representation16. , we escorted these $380,000 worth ofMedical EquipmentCompleted the last mile from air transport to customer warehouses. This case is particularly noteworthy as it highlights three key challenges in medical device imports: complex declaration requirements, strict quarantine inspections, and tight timelines.
18. When taking on this project, the client was most concerned about two issues: whether the Japanese beauty devices could be imported smoothly as medical devices, and whether clearance could be completed before National Day. Our solution was: conduct pre-shipment inspections in advance, prepare complete medical device filing documents, and chooseAir Transportation19. + airport clearance fast track. The actual clearance took only 3 working days (including inspection), 40% faster than the industry average.
21. Many people dont realize that the biggest hurdle in beauty device imports isnt tariffs but medical device registration and filing. According to Chinas Regulations on the Supervision and Administration of Medical Devices, RF beauty devices fall under Class II medical devices and must provide:
Our team completed two critical actions before the goods took off: first, coordinating with Japanese suppliers to obtain JETRO-certified pre-shipment inspection reports; second, submitting the import medical device filing application to the Shanghai Medical Products Administration in advance. This pre-clearance model was later called the clearance code by clients, effectively avoiding regulatory detention after goods arrive at the port.
28. At 10:15 AM on Monday, September 26, the goods landed at Pudong Airport on time. Our on-site team had already prepared all electronic declaration documents:
After completing the declaration at 14:30 that afternoon, the customs system randomly selected our shipment for inspection. Heres a professional detail: medical device inspections typically involve joint checks by drug regulatory authorities. Because we had completed the filing in advance, we passed the quality and safety inspection the next day. On Wednesday, September 28, after the client paid the 6.5% tariff and 13% VAT in the morning, the system showed released at 12:08 noon.
36. This cases success was no accident—it relied on three core capabilities accumulated over 15 years of import agency:
Advantage dimensions | Specific manifestations |
---|---|
Policy anticipation | 37. Predicting medical device import regulations tightening 3 months in advance, advising clients to upgrade product certifications |
Process Optimization | Through the pre-declaration + electronic release model, airport customs clearance was compressed to within 72 hours |
Emergency Handling | 39. Establishing emergency contact mechanisms with Shanghai Airport Customs, Inspection and Quarantine, and Drug Regulators |
40. Special note: since 2023, customs has new interpretations for beauty device classification. Some therapeutic devices may be classified under 9018 instead of 9506, directly affecting tariff rates and regulatory requirements. In another recent case, our professional classification advice saved a client 9% in tariffs.
41. Based on this case, here are three suggestions for companies planning to import beauty devices:
49. Recently, we helped a client process a Japanese beauty devices3C50. certification exemption application. If you encounter similar issues during import, feel free to contact us. In thisimport and export51. industry, sometimes one correct classification advice can justify the entire agency fee.
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