其次，经营企业要知晓办理三类医疗器械经营许可证需要准备哪些资料。
(1)提交医疗器械经营企业许可证申请表，法定代表人签字或加盖企业公章；
(2)工商行政管理部门出具的企业名称预核准证明文件或《营业执照》复印件和校验原件；
(3)企业质量管理负责人的身份证、学历或者职称证明复印件及个人简历；质量管理人员的身份证、学历或者职称证明复印件；
(4)经营场所、仓库的地理位置图、平面图（注明面积）、房屋产权证明或者租赁协议复印件；
(5)企业产品质量管理制度文件及储存设施、设备目录。
(6）对于办理三类医疗器械经营许可证内容包含有需要冷藏的药品时，企业具备的运输装备、仓储设施设备情况表。
、第三类医疗器械经营许可证怎么办理
（1）申请人提交申请资料到相关部门；
（2）相关部门受理申请人的申请；
（3）到实际场地进行勘察以及对产品进行审核；
（4）准予颁发三类医疗器械许可证。
certificate and personal resume of the management manager of the enterprise; a copy of the ID card, educational background or professional title certificate of the management personnel; (4) The business site, warehouse of the geographical location plan, plan (indicating the area), the property right certificate or lease copy of the agreement; (5) Enterprise product management system documents and catalogue of storage facilities and e (6) Table of transportation e and storage facilities and e available by the enterprise when the contents of the business license contains drugs that need to be refrigerated. , The third type of medical e business license how to handle (1) The applicant shall submit the application materials to the relevant departments; (2) Relevant departments shall accept the application of the applicant; (3) Investigate the actual site and audit the pr
