現場審核：申請材料提交后，醫(yī)療器械監(jiān)督管理部門將對企業(yè)進行現場審核，包括場地、人員、質量管理、醫(yī)療器械采購、銷售等方面的審核。

預審：現場審核合格后，醫(yī)療器械監(jiān)督管理部門將對申請材料進行預審。

審核：預審合格后，醫(yī)療器械監(jiān)督管理部門將進行審核，審核包括企業(yè)的組織架構、質量管理體系、產品銷售情況等方面。

頒發(fā)許可證：審核通過后，醫(yī)療器械監(jiān)督管理部門將頒發(fā)醫(yī)療器械經營許可證。

申請三類醫(yī)療器械經營許可證需要滿足相關的資質要求和管理要求，申請過程比較復雜，建議企業(yè)在申請前了解相關政策法規(guī)，以及咨詢專業(yè)的醫(yī)療器械代辦公司或律師事務所，提高申請成功率

隨著相關制度的逐步完善，市場環(huán)境的逐漸向好，醫(yī)療器械或將迎來噴涌爆發(fā)式的發(fā)展。

s are submitted, the medical device supervision and administration department will conduct on-site audit of the enterprise, including site, personnel, management, medical device procurement and sales. Pre-examination: After passing the on-site examination, the medical device supervision and administration department will conduct pre-examination of the application materials. Audit: After the pre-examination, the medical device supervision and management department will conduct an audit, including the organizational structure, management system, product sales, etc. License issuance: After the approval, the medical device supervision a