(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。
二、第三类医疗器械经营许可证办理流程:
1、经营企业经办人携带上述资料前往监督管理部门申请经营许可;
2、工作人员受理资料,并于30个工作日内进行审查,必要时组织核查;
3、对符合规定条件的,准予许可并发给医疗器械经营许可证;对不符合规定条件的,不予许可并书面说明理由。
三、第三类医疗器械经营许可证办理所需材料:
1、企业名称与经营范围,注册资本及股东出资比例,股东等sfz明;
2、医疗器械产品注册证书、供应商营业执照、许可证及授权书;
for handling the business license of Class III Medical Devices:1. The operator of the operating enterprise shall apply to thesupervision and administration department for the business licensewith the above information; 2. The staff shall accept thematerials, and review them within 30 working days, and organize theverification if necessary; 3. Grant license and medical deviceoperation license for those who meet the prescribed conditions, andgive reasons in writing. 3. Materials required for handling thebusiness license of Class III medical devices: 1, the enterprisename and business scope, the registered capital and the proportionof shareho