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!
企业设立流程:
1、企业名称核准，建议多准备几个名称，名称核售通过之后领取《企业名称核生通知书》;
2、领取《公司设立登记申请书》，并且填写齐全
3、租赁实际地址，医疗器械公司注册的注册条件之一就是需要实际地址，所以申请人一定要租便实际的办公地址才可以，这个后期药监局的也是会辰人来
审直的。
4、准备注册材料，《公司设立登记申请书》、《企业名称械准通知书》、注册地址、经营范围、注册咨本、法人股东身份信息等等，按照预的时间向工商