门头沟大峪北京医疗器械二类备案医疗器械三类经营许可证专业办理经验丰富靠谱周期短Zui快7天下证

（1）企业营业执照；

（2）公司章；

（3）房屋产权证明、租赁协议；

（4）法定代表人、主要负责人、品质管理员的身份、毕业证等证明材料；

（5）经营地平面设计图，仓库平面设计图。

申请办理三类医疗器械许可证的规定

（1）场所和仓库总面积规定：与经营地企业规模相一致。

（2）品质管理员规定：专科本科以上学历或是初级左右专业职称，另外理应具备3年左右医疗器械经营品质管理方面亲身经历。

（3）品质管理员技术专业规定：医疗机械有关技术专业，例如：医药学、药理学、生物技术、护理专业等。

三类医疗器械许可证怎么样办

ase agreement; (4) Identity of legal representative, principal person in charge, quality manager, graduation certificate and other certification materials; (5) Business floor plan design drawing, warehouse floor plan design drawing. Provisions on applying for a class III medical device license (1) The total area of the place and warehouse: consistent with the scale of the enterprise in the operating place. (2) Quality administrator regulations: college degree or above or junior professional title, in addition, should have about 3 years of personal experience in medical device business quality management. (3) Technical professional regulations of quality administrators: related technical majors of medical machinery, such as medicine, pharmacology, biotechnology, nursing majors, etc.