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

3、對(duì)符合規(guī)定條件的，準(zhǔn)予許可并發(fā)給醫(yī)療器械經(jīng)營(yíng)許可證；對(duì)不符合規(guī)定條件的，不予許可并書(shū)面說(shuō)明理由。

三、第三類(lèi)醫(yī)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(cè)資本及股東出資比例，股東等sfz明；

2、醫(yī)療器械產(chǎn)品注冊(cè)證書(shū)、供應(yīng)商營(yíng)業(yè)執(zhí)照、許可證及授權(quán)書(shū)；

3、質(zhì)量管理文件等；

4、2個(gè)或以上醫(yī)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；

5、符合醫(yī)療器械經(jīng)營(yíng)要求的辦公場(chǎng)地及倉(cāng)庫(kù)證明；

6、公司章程、股東會(huì)決議等；

7、財(cái)務(wù)人員sfz和上崗證；

8、其它相關(guān)材料。

 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 contribution, shareholders and other sfz Ming; 2. Medical device product registration certificate, supplier business license, license and authorization letter; 3. management documen