(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。
2、法律依据:《医疗器械监督管理条例》第十四条
第一类医疗器械产品备案和申请第二类、第三类医疗器械产品注册,应当提交下列资料:
(一)产品风险分析资料;
(二)产品技术要求;
(三)产品检验报告;
(四)临床评价资料;
(五)产品说明书以及标签样稿;
(六)与产品研制、生产有关的质量管理体系文件;
(七)证明产品安全、有效所需的其他资料。
医疗器械二类备案流程:1、准备执照副本,公章,实际经营地址房本复印件,租房合同2、需要提供一名质量管理员,医学医护相关专业毕业满3年的3、网上提交医疗器械二类备案审核资料通过后线下交材料 4、经营医疗器械二类批发的企业还需要准备库房 可全程免费指导办理流程,提供质量管理员,也可托管办理,专业速度快速*快3天完成备案
2) Relevant departments shall accept the application of theapplicant; (3) Investigate the actual site and audit the products;(4) Grant the issuance of a class III medical device license. 2.Legal basis: Article 14 of the Regulations on the Supervision andAdministration of Medical Devices As for the registration of ClassII and III medical devices, the following materials shall besubmitted: (1) Product risk analysis data; (2) Technicalrequirements for the products; (3) Product inspection report; (4)Clinical evaluation data; (5) Product specification and labelsamples; (6) quality management system documents related to productdevelopment and production; (7) other materials required to provethe safety and effectiveness of the product. Medical equipment 2filing process: 1, to prepare the license copy, official seal, theactual business address room this copy, rental contract 2, need toprovide a quality administrator, medical related professionalgraduate full 3 years of 3, online medical device 2 filing auditdata through offline material 4, medical equipment 2 wholesaleenterprises also need to prepare warehouse can guide process, freeprovide quality administrator, also can hosting, professional speedfast fastest 3 days to complete for the record