A certain provinceMedical EquipmentTypical case encountered by an importer in 2024: Self-declared CT equipment triggered customs three-level warning system due to undeclared radioactive components. This not only resulted in goods return but also placed the company on a key supervision list, directly affecting subsequent three batches of equipment import plans worth EUR 20 million.
Technical parameter misinterpretation riskTechnical indicator differences between EU CE certification and domestic GB standards
Logistics disassembly trapTariff determination disputes during split transportation of large equipment
Post-supervision blind spots:3CAnnual certification maintenance and usage reporting requirements
Full-process value decomposition of agency services
Professional agency approval throughFour-dimensional risk control systemEnsuring equipment import safety:
Equipment import trend forecast for the next three years
According to the 2025-2027 Customs Supervision Reform Roadmap, equipment imports will face:Full implementation of intelligent document review systems,Whole-life-cycle traceability systemsEstablishment,Dynamic early warning for technical trade measuresand other new challenges. Professional agencies have pre-deployed AI customs declaration pre-review systems and established direct data connections with major ports to ensure clients maintain customs clearance efficiency advantages under the new regulatory environment.