聘請專業(yè)人員：聘請具有相關醫(yī)療器械經營經驗的專業(yè)人員，如負責人、注冊人員、經營管理人員、技術人員等。

提交申請材料：提交申請材料包括醫(yī)療器械經營許可證申請表、醫(yī)療器械經營許可證頒發(fā)范圍的說明、公司營業(yè)執(zhí)照、組織機構代碼證、稅務登記證、法人代表身份證、醫(yī)療器械經營負責人和技術人員的聘書、企業(yè)的藥品經營質量管理規(guī)范制度及其實施情況、醫(yī)療器械的采購渠道、銷售情況等。

現(xiàn)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(xiàn)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(xiàn)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

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 and administration department will issue the medical device business license. The application for the business license of Class III medical devices needs to meet the relevant re and management re, and the application process is quite complicated. It is suggested that enterprises understand the relevant policies and regulations before applying, as well as consulting professional medical devices