三类医疗器械经营许可证如何办理
1、三类医疗器械经营许可证办理方式如下：
（1）申请人提交申请资料到相关部门；
（2）相关部门受理申请人的申请；
（3）到实际场地进行勘察以及对产品进行审核；
（4）准予颁发三类医疗器械许可证。
三类医疗器械作为目前医疗器械分类中危险性最高的品类，严格受到相关部门的监督和管理，但是对于很多经营三类医疗器械的家人们来说，很多基础性问题还不能完全掌握，今天我们就来看一看，三类医疗器械经营范围有哪些？又该如何申请三类医疗器械经营许可证！
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 equipment business license again!
三类，医疗器械属于风险较大的医疗器械，需要采取特殊措施严格控制，确保安全有效的医疗器械，如：输液器、注射器、静脉留置针、支架、呼吸机、 CT、核磁共振等，其产品及生产经营活动由国家总局、省级食品药品监管部门以及设区的市食品药品监管部门分别颁发《医疗器械注册证》，《医疗器械生产许可证》，《医疗器械经营许可证》。