1, pre-approval of the enterprise name;
2, to provide personnel and product-related materials (the enterprise is responsible for), while the decoration and layout of the office and the warehouse
3, complete materials, in the Food and Drug Administration Web site to submit an application;
4, the online application review and approval, the submission of a full set of written materials to the Drug Administration
5, the Drug Administration review of written application materials through the notice of acceptance of the site time;
6, acceptance of the site (need to be all the personnel of the enterprise to the scene);
7, site acceptance, Drug Administration approval of the license;
8, to receive the "Medical Device Business License";
9, Account opening capital verification;
10, for the three certificates (business license, organization code certificate, tax registration certificate).