2, belonging to the "implementation of mandatory product certification of medical devices within the product catalog", should provide China Compulsory Certification (3C); 3, some of the equipment required to apply for an automatic import license (O certificate);
4, photos of the equipment
4, photos of the equipment, nameplates, technical parameters of the equipment, end use, Chinese manuals, etc.;
5, import contracts, box lists,
6, other materials need to be supplemented.