1, the State Food and Drug Administration issued by the registration of imported medical equipment and business licenses;
2, belonging to the meaning of pharmaceutical components of the medical equipment, should provide China Compulsory Certification (Special Goods Approval Sheet);
3, some of the equipment needs automatic import license (O certificate)
4, equipment photos, nameplates, equipment, technical parameters, end use, Chinese manuals, etc.;
5, import contracts, packing lists, invoices;
6, other materials to be added.