朝阳西坝北京医疗器械三类经营许可证，医疗器械二类备案提供人员库房专业快捷包下证。

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。

of the pre-approval certificate of enterprise name or thebusiness license issued by the administrative department forindustry and commerce; (3) a copy of the id card, educationalbackground or professional title certificate and personal resume ofthe management manager of the enterprise; a copy of the idcard, educational background or professional title certificate ofthe management personnel; (4) the business site, warehouseof the geographical location plan, plan (indicating the area), theproperty right certificate or lease copy of the agreement; (5)enterprise product management system documents andcatalogue of storage facilities and e (6) table oftransportation e and storage facilities and eavailable by the enterprise when the contents of the businesslicense contains drugs that need to be refrigerated. , the thirdtype of