括场地、人员、质量管理、医疗器械caigou、销售等方面的审核。
预审：现场审核合格后，医疗器械监督管理部门将对申请材料进行预审。
审核：预审合格后，医疗器械监督管理部门将进行审核，审核包括企业的组织架构、质量管理体系、产品销售情况等方面。
颁发许可证：审核通过后，医疗器械监督管理部门将颁发医疗器械经营许可证。
申请三类医疗器械经营许可证需要满足相关的资质要求和管理要求，申请过程比较复杂，建议企业在申请前了解相关政策法规，以及咨询专业的医疗器械代办公司或律师事务所，提高申请成功率
随着相关制度的逐步完善，市场环境的逐渐向好，医疗器械或将迎来喷涌爆发式的发展。
新政策要求：医疗器械经营企业要在经营活动中积极应用唯一标识，做好带码入库、出库，实现产品在流通环节可追溯。
医疗器械经营许可证申请须知
医疗器械经营许可证是医疗器械经营企业必须具备的，开办第二类医疗器械经营企业，应当向省、自治区、直辖市人民zhengfu药品监督管理部门备案；
开办第三类医疗器械经营企业，应当经省、自治区、直辖市人民zhengfu药品监督管
cal device agency companies or law firms, so as to improve thesuccess rate of the application With the gradual improvement ofrelevant systems and the gradual improvement of the marketenvironment, medical devices may usher in the explosivedevelopment. The new policy requirements: medical device operatingenterprises should actively apply the unique identification intheir business activities, do a good job of warehousing andwarehousing with codes, and realize the traceability of products inthe circulation link. Instructions for application of medicalDevice Business License The medical device business license isnecessary for the medical device trading enterprise, and theestablishment of the second class medical device trading enterpriseshall be filed by the drug regulatory department of the
