(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;
6、公司章程、股东会决议等;
7、财务人员sfz和上岗证;
8、其它相关材料。
医疗器械是一种用于预防、诊断、治疗或缓解疾病或残疾的工具、设备、仪器或机器。它们包括各种医用产品,如手术器械、医用材料、注射器、心脏起搏器、医疗椅等等。医疗器械行业的发展
hall 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. 2. Legal basis: Article 14 of the Regulations on the Supervision and Administration of Medical Devices As for the registration of Class II and III medical devices, the following materials shall be submitted: (1) Product risk analysis data; (2) Technical requirements for the products; (3) Product inspection report; (4) Clinical evaluation data; (5) Product specification and label samples; 6. Articles of association, resolutions of shareholders' meeting, etc.; 7, financial personnel sfz and work certificate; 8. Other related materials. A medical device is a tool, device, instrument, or machine used for the prevention, diagnosis, treatment, or mitigation of illness or disability. They include a variety of medical products such as surgical instruments, medical materials, syringes, pacemakers, medical chairs and more. The development of the medical device industry