預(yù)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(yù)審。

審核：預(yù)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(gòu)、質(zhì)量管理體系、產(chǎn)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(jīng)營許可證。

申請三類醫(yī)療器械經(jīng)營許可證需要滿足相關(guān)的資質(zhì)要求和管理要求，申請過程比較復(fù)雜，建議企業(yè)在申請前了解相關(guān)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(wù)所，提高申請成功率

隨著相關(guān)制度的逐步完善，市場環(huán)境的逐漸向好，醫(yī)療器械或?qū)⒂瓉韲娪勘l(fā)式的發(fā)展。

新政策要求：醫(yī)療器械經(jīng)營企業(yè)要在經(jīng)營活動中積極應(yīng)用唯一標識，做好帶碼入庫、出庫，實現(xiàn)產(chǎn)品在流通環(huán)節(jié)可追溯。

醫(yī)療器械經(jīng)營許可證申請須知

醫(yī)療器械經(jīng)營許可證是醫(yī)療器械經(jīng)營企業(yè)必須具備的，開辦第二類醫(yī)療器械經(jīng)營企業(yè)，應(yīng)當向省、自治區(qū)、直轄市人民政府藥品監(jiān)督管理部門備案；

開辦第三類醫(yī)療器械經(jīng)營企業(yè)，應(yīng)當經(jīng)省、自治區(qū)、直轄市人民政府藥品監(jiān)督管理部門審查批準，并發(fā)給《醫(yī)療器械經(jīng)營許可證》。

依據(jù)《醫(yī)療器械經(jīng)營監(jiān)督管理辦法》，開設(shè)三類醫(yī)療器械運營公司，食品類藥品監(jiān)督管理局單位將會對經(jīng)營地開展當場審查。對不符合要求標準的，明確提出整頓規(guī)定或未予批準。根據(jù)《藥品醫(yī)療器械飛行檢查辦法》，食品類藥品監(jiān)督管理局單位將會對醫(yī)療機械銷貨方式合理合法、工作人員在職人員在職、拿貨檢查、運送儲存等層面開展不事先告之的監(jiān)督管理。三類醫(yī)療器械的界定

nt 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 should meet the relevant re and management re, and the application process is complicated. It is suggested that enterprises understand the relevant policies and regulations before the application, as well as consult professional medical device agency companies or law firms, so as to improve the success rate of the application With the gradual improvement of relevant systems and the gradual improvement of the market environment, medical devices may usher in the explosive development. The new policy re: medical device operating enterprises should actively apply the unique identification in their business activities, do a good job of warehousing and warehousing with codes, and realize the traceability of products in the circulation link. Instructions for application for medical Device Busi