（2）相關(guān)部門(mén)受理申請人的申請；

（3）到實(shí)際場(chǎng)地進(jìn)行勘察以及對產(chǎn)品進(jìn)行審核；

（4）準予頒發(fā)三類(lèi)醫療器械許可證。

二、第三類(lèi)醫療器械經(jīng)營(yíng)許可證辦理流程：

1、經(jīng)營(yíng)企業(yè)經(jīng)辦人攜帶上述資料前往監督管理部門(mén)申請經(jīng)營(yíng)許可；

2、工作人員受理資料，并于30個(gè)工作日內進(jìn)行審查，必要時(shí)組織核查；

3、對符合規定條件的，準予許可并發(fā)給醫療器械經(jīng)營(yíng)許可證；對不符合規定條件的，不予許可并書(shū)面說(shuō)明理由。

三、第三類(lèi)醫療器械經(jīng)營(yíng)許可證辦理所需材料:

1、企業(yè)名稱(chēng)與經(jīng)營(yíng)范圍，注冊資本及股東出資比例，股東等sfz明；

2、醫療器械產(chǎn)品注冊證書(shū)、供應商營(yíng)業(yè)執照、許可證及授權書(shū)；

3、質(zhì)量管理文件等；

4、2個(gè)或以上醫學(xué)專(zhuān)業(yè)或相關(guān)專(zhuān)業(yè)人員證書(shū)、sfz明與簡(jiǎn)歷；

 application of the applicant; (3) Investigate the actual site and audit the products; (4) Grant the issuance of a class III medical device license. 2. Process for handling the business license of Class III Medical Devices: 1. The operator of the operating enterprise shall bring the above information to the supervision and administration department to apply for the business license; 2. The staff shall accept the materials, and review them within 30 working days, and organize the verification if necessary; 3. Grant license and medical device operation license for those who meet the prescribed conditions, and give reasons in writing. 3. Materials required for handling the business license of Class III medical devices: 1, the enterprise name and business scope, the registered capital and the proportion of shareholder