（2）相關部門受理申請人的申請；

（3）到實際場地進行勘察以及對產品進行審核；

（4）準予頒發(fā)三類醫(yī)療器械許可證。

二、第三類醫(yī)療器械經營許可證辦理流程：

1、經營企業(yè)經辦人攜帶上述資料前往監(jiān)督管理部門申請經營許可；

2、工作人員受理資料，并于30個工作日內進行審查，必要時組織核查；

3、對符合規(guī)定條件的，準予許可并發(fā)給醫(yī)療器械經營許可證；對不符合規(guī)定條件的，不予許可并書面說明理由。

三、第三類醫(yī)療器械經營許可證辦理所需材料:

1、企業(yè)名稱與經營范圍，注冊資本及股東出資比例，股東等sfz明；

2、醫(yī)療器械產品注冊證書、供應商營業(yè)執(zhí)照、許可證及授權書；

3、質量管理文件等；

4、2個或以上醫(yī)學專業(yè)或相關專業(yè)人員證書、sfz明與簡歷；

 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