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;
filing, you need to provide: 1. Legal person identityinformation; 2. Identity information of the quality personnel; 3.Copy of the company's business license 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)