我們必須清楚辦理醫(yī)療器械三類經(jīng)營(yíng)許可證需要哪些資料；

1、公司執(zhí)照正副本

2、公章

3、辦公和庫房房本復(fù)印件

4、人員（主要是質(zhì)量管理人和主管檢驗(yàn)師）

其中 質(zhì)量管理人：要求大專畢業(yè)滿三年

主管檢驗(yàn)師：要求本科畢業(yè)滿三年 檢驗(yàn)學(xué)相關(guān)專業(yè)

辦理醫(yī)療器械三類經(jīng)營(yíng)許可證要完成以下流程：

1、經(jīng)營(yíng)范圍要有“銷售醫(yī)療器械”

2、網(wǎng)申提交醫(yī)療器械材料

3、藥監(jiān)窗口提交三類材料（攜帶原件），等待通知核查

4、領(lǐng)取醫(yī)療器械許可證（若有二類，提交材料，當(dāng)天下備案單）

最后明晰辦理醫(yī)療器械三類經(jīng)營(yíng)許可證有效期、辦理期限：

ager and the supervisor inspector) Among them, manager: required college graduation for three years Supervisor inspector: required to graduate for three years of laboratory related major Secondly, the following procedures should be completed for the third business license of medical devices: 1, the business scope should have "sales of medical devices" 2. Submit medical device materials online application 3. The drug administration window shall submit three types of materials (carry the original) and wait for notification and verification 4. Get the medical device license (if there is class II, submit materials, the world record) Finally, the validity period and processi