海淀温泉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人员专业快捷包下证。

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、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、提交完毕后需要准备以下资料去现场提交材料

1.）《医疗器械经营许可证申请表》

2）《营业执照正副本原件)(复印件)

3）法定代表人、企业负责人、质量负责人的身份证明、学历或者职称证明复印件；

4.）组织机构与部门设置说明

need to provide: 1. Legal person identity information; 2.Identity information of the quality personnel; 3. The company'sbusiness license principal, secondary copy and official seal; 4.Warehouse address materials; Procedures for handling the businesslicense of Class III medical devices 1. First of all, to networkaccess, apply for the medical device business license to fill inthe company's relevant information and submit. 2. After thesubmission, the next step needs to prepare the following materialsto submit the materials on site 1.) Application Form for MedicalDevice Business License 2) Original copy of business License)(photocopy) 3) Copy of the identity certificate, educationalbackground or professional title certificate of the legalrepresentative, the person in charge of the enterprise and theperson in charge of quality; 4.) Description of organizationstructure and department setting