三類醫(yī)療器械經營許可證如何辦理
1、三類醫(yī)療器械經營許可證辦理方式如下：
（1）申請人提交申請資料到相關部門；
（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。

三類醫(yī)療器械作為目前醫(yī)療器械分類中危險性最高的品類，嚴格受到相關部門的監(jiān)督和管理，對于很多經營三類醫(yī)療器械的家人們來說，很多基礎性問題還不能完全掌握，今天我們就來看一看，三類醫(yī)療器械經營范圍有哪些？又該如何申請三類醫(yī)療器械經營許可證！

handle the business license of class III medical devices
1. The business license of Class III medical devices is handled as follows:
(1) The applicant shall submit the application materials to the relevant departments;
(2) Relevant departments shall accept the application of the applicant;
(3) Investigate the actual site and audit the products;
(4) Grant the issuance of a class III medical device license.

Three kinds of medical devices as the highest risk in the medical device classification category, strictly by the supervision and management, but for many families of three kinds of medical devices, many basic problems is not fully grasp, today we will take a look, what are three business scope of medical devices? How to apply for the three types of medical e business license again!

二、三類醫(yī)療器械經營許可證辦理所需材料

1、需要3名相關醫(yī)學專業(yè)畢業(yè)的大專以上(含大專)文憑產品質量監(jiān)督檢測人員(其中一個為質量檢測負責人);

2、三名質量監(jiān)督檢測人員的身份證和畢業(yè)證復印件、工作簡歷;(食品藥監(jiān)局老師過來場地核查約談的時候需要提供相關檢測人員的身份證和畢業(yè)證原件，并本人到場);

3、銷售醫(yī)療器械需要相應公司營業(yè)執(zhí)照、醫(yī)療器械生產企業(yè)許可證;

4、售醫(yī)療器械對方生產廠家的醫(yī)療器械注冊證、醫(yī)療器械注冊登記表;

5、銷售醫(yī)療器械對方生產廠家的委托銷售授權書;