朝阳慈云寺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，

三类申请医疗器械经营许可证条件：

1.具有与经营规模和经营范围相适应的质量管理机构或者专职质量管理人员。质量管理人员应当具有国家认可的相关专业学历或者职称；

2.具有与经营规模和经营范围相适应的相对独立的经营场所；

3.具有与经营规模和经营范围相适应的储存条件，包括具有符合医疗器械产品特性要求的储存设施、设备；

4.应当建立健全产品质量管理制度，包括采购、进货验收、仓储保管、出库复核、质量跟踪和不良事件的报告制度等；

5.应当具有与其经营的医疗器械产品相适应的技术培训和售后服务的能力，或者约定由第三方提供技术支持；

6.经营无菌和植入类产品的公司需建立计算机管理系统及计算机管理制度，能够保证产品从购进到销售整个过程的有效质量跟踪和追溯。

申请医疗器械经营许可证所需材料：

It shall have a quality management institution or full-timequality management personnel suitable for the business scale andbusiness scope. The quality management personnel shall have therelevant professional academic qualifications or professionaltitles recognized by the state; 2. Having a relatively independentbusiness site commensurate with the scale and scope of business; 3.Having storage conditions suitable with the scale and scope ofbusiness, including storage facilities and equipment that meet therequirements of the characteristics of medical device products; 4.The product quality management system shall be established andimproved, including procurement, purchase acceptance, storage,warehouse delivery review, quality tracking and adverse eventreporting system; 5. It shall have