With theMedical EquipmentThe 2025 Edition of the Classification Catalogue is officially implemented, laboratoryequipment. 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.The regulatory system presents three major changes:Refinement of equipment classification,Standardization of declaration documentsandStrengthening of quality traceabilityAmong them, 23 types of equipment such as PCR instruments and biosafety cabinets have new dynamic supervision requirements. Importers need to pay special attention to the continuation conditions of the tax - free policy for scientific research equipment in Announcement No. 89 of the General Administration of Customs.
CompliantImport RepresentationService providers must possess the following qualification matrix simultaneously:
When choosing an import service provider, six dimensions should be focused on:
Provide solutions for common business scenarios:
According to the latest regulatory requirements, the necessary documents include:
The recent regulatory focus is on:Refurbishment markings for used equipment,Compatibility between software version and hardware,Proportion of accompanying consumablesThree aspects. It is recommended to clarify the suppliers liability clauses at the contract - signing stage, reserve 10% of the balance as a quality guarantee, and stipulate that the relevant clauses of the United Nations Convention on Contracts for the International Sale of Goods shall apply to dispute resolution.
? 2025. All Rights Reserved. Shanghai ICP No. 2023007705-2 PSB Record: Shanghai No.31011502009912