丰台卢沟桥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人员专业快捷包下证，

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：

医疗器械经营许可证办理依据《北京市实施细则（2017年修订版）》，具体提交材料如下：

1．《 医疗器械经营许可申请表》（原件1份）

2．《营业执照》复印件（交验原件）；（复印件1份）

nt system shall be established and improved, includingprocurement, purchase acceptance, storage, warehouse deliveryreview, quality tracking and adverse event reporting system; 5. Itshall have the ability of technical training and after-salesservice suitable with the medical device products it operates, oragree to provide technical support by a third party; 6. Companiesoperating sterile and implanted products shall establish a computermanagement system and a computer management system to ensure theeffective quality tracking and traceability of the whole process ofproducts from purchase to sales. Materials required for applyingfor the Medical Device Business License: The medical devicebusiness license is handled according to the ImplementationRule