1, the State Food and Drug Administration issued by the registration of imported medical equipment and business license;
2, belonging to the meaning of pharmaceutical components of the medical equipment, should provide China Compulsory Certification (Special Goods Approval Sheet);
3, part of the equipment requires automatic import license (O certificate);
4, photos of the equipment, nameplates, technical parameters of the equipment, end use, Chinese manuals, etc.;
5, import contracts, packing lists, invoices;
6, other materials need to be supplemented.
The above content can be used for reference, detailed according to the type of imported medical equipment, import port and other factors.