海淀香山北京医疗器械三类经营许可证，医疗器械二类备案提供进销存软件库房速度快专业方便

依据《医疗器械监督管理条例》，第三类医疗器械是具备较高危，必须采用非常对策严控管理方法以确保其安全性、合理的医疗机械。例如普遍的注射器、注射针、静脉留置针、心脏支架、麻醉机、ct、磁共振等。

申请办理三类医疗器械许可证必须提前准备的原材料

（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

充分考虑医药行业相关法律法规及管控规定许多，跨专业工作人员没办法申请办理取得成功或产生后遗症，

提议找医疗器械专业第三方服务项目组织申请办理。由于第三方资源广，基础的法律法规都一清二楚，提前准备材料自然游刃有余。

 prepared in advance when applying for the class iiimedical device license (1) enterprise business license; (2) companyseal; (3) property right certificate and lease agreement; (4)identity of legal representative, principal person in charge, manager, graduation certificate and other certificationmaterials; (5) business floor floor design drawing, warehouse floordesign drawing. provisions for applying for a class iii medicaldevice license (1) the total area of the place and warehouseprovisions: consistent with the scale of the enterprise in theplace of operation. (2) administrator regulations: collegedegree or above or junior professional title, in addition, shouldhave about 3 years of personal experience in medical devicebusiness management. (3) technical professional regulationsof administrators: related technical majors of medicalmachinery, such as medicine, pharmacology, biotechnology, nursingmajors, etc. how to do the third-class medical device license fullyconsidering the relevant laws and regulations and controlprovisions of the pharmaceutical industry, cross-professional staffcannot apply for success or sequelae, i propose to apply for aprofessional third-party service project of medical devices. due tothe wide range of third-party resources, the basic laws andregulations are all clear, so it is na