提交申請(qǐng)材料：提交申請(qǐng)材料包括醫(yī)療器械經(jīng)營(yíng)許可證申請(qǐng)表、醫(yī)療器械經(jīng)營(yíng)許可證頒發(fā)范圍的說(shuō)明、公司營(yíng)業(yè)執(zhí)照、組織機(jī)構(gòu)代碼證、稅務(wù)登記證、法人代表身份證、醫(yī)療器械經(jīng)營(yíng)負(fù)責(zé)人和技術(shù)人員的聘書(shū)、企業(yè)的藥品經(jīng)營(yíng)質(zhì)量管理規(guī)范制度及其實(shí)施情況、醫(yī)療器械的采購(gòu)渠道、銷售情況等。

現(xiàn)場(chǎng)審核：申請(qǐng)材料提交后，醫(yī)療器械監(jiān)督管理部門將對(duì)企業(yè)進(jìn)行現(xiàn)場(chǎng)審核，包括場(chǎng)地、人員、質(zhì)量管理、醫(yī)療器械采購(gòu)、銷售等方面的審核。

預(yù)審：現(xiàn)場(chǎng)審核合格后，醫(yī)療器械監(jiān)督管理部門將對(duì)申請(qǐng)材料進(jìn)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(jìn)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(guò)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(yíng)許可證。

申請(qǐng)三類醫(yī)療器械經(jīng)營(yíng)許可證需要滿足相關(guān)的資質(zhì)要求和管理要求，申請(qǐng)過(guò)程比較復(fù)雜，建議企業(yè)在申請(qǐng)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(qǐng)成功率

隨著相關(guān)制度的逐步完善，市場(chǎng)環(huán)境的逐漸向好，醫(yī)療器械或?qū)⒂瓉?lái)噴涌爆發(fā)式的發(fā)展。

新政策要求：醫(yī)療器械經(jīng)營(yíng)企業(yè)要在經(jīng)營(yíng)活動(dòng)中積極應(yīng)用唯一標(biāo)識(shí)，做好帶碼入

lication materials including medical device business license application form, the scope of medical device business license, company business license, organization code certificate, tax registration certificate, legal representative id card, medical e management and appointment of technical personnel, the enterprise drug management management system and its implementation, medical e procurement channels, sales, etc. On-site audit: After the application materials 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