顺义建新北京医疗器械三类经营许可证，医疗器械二类备案提供进销存软件库房速度快专业方便，

如果您不知道自己的产品是什么类型的，可以打电话随时咨询我，可以给您妥善的建议。

办理医疗资质许可证，您需要具有相关的人员，库房地址以及产品编号，我司均可以为您提供。

办理二类备案您需要提供：

1.法人身份信息；

2.质量员身份信息；

3.公司营业执照正副本以及公章；

4.库房地址材料；

三类医疗器械经营许可证办理流程

一、首先要网登，申请医疗器械经营许可证填写公司相关资料并提交。

二、提交完毕后接下来需要准备以下资料去现场提交材料

an give you proper advice. For the medical qualification license, you need to have the relevant personnel, warehouse address and product number, our company can provide it for you. For Class II filing, you need to provide: 1. Legal person identity information; 2. Identity information of the quality personnel; 3. Copy of the business license and official seal; 4. Warehouse address materials; Procedures for handling the business license of Class III medical devices 1. First of all, to network access, apply for the medical device business license to fill in the company's relevant information and submit. 2. After the submission, the ne