房山韩村河北京医疗器械二类备案医疗器械三类经营许可证全程托管省心安全Zui快七天下证

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

 and hold the certificate; 3, product requirements: must have the product information in accordance with the business scope, and issue a certificate; 4. Other relevant laws and regulations and requirements. 3. Procedures for obtaining the Class III Medical Device License: 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. The above is the relevant introduction of the three types of medical device business license processing, the procedures may be more cumbersome.