被委托方签署的书面协议复印件、被委托方的《医疗器械经营许可证》复印件）
5.企业设施设备情况（原件1份）。（内容包含：经营设施、设备目录、经营质量管理制度、工作程序等文件目录、计算机信息管理系统基本情况介绍和功能说明）（原件1份）
6．企业真实性保证材料（原件1份）。（内容包含：申报材料真实性的自我保证声明，并对材料作出如有虚假承担法律责任的承诺、凡申请企业申报材料时，具体办理人员不是法定代表人或负责人本人的，企业应当提交《授权委托书》
三类医疗器械许可证经营范围包括:医用电子仪器设备，医用光学器具、仪器及内窥镜设备，医用磁共振设备，医用X射线设备，手术室、急救室、诊疗室设备及器具。售卖医疗器械必须办理经营许可
证，根据相关法律规定，国家食品药品监督管理局逐步推行医疗器械经营质量规范管理制度。医疗器械经营质量管理规范由国家食品药品监管管理局组织制定。
formation (1 original copy).(Contents include: businessfacilities, equipment catalogue, business quality managementsystem, working procedures and other documents catalogue, basicinformation introduction of computer information management systemand function description) (1 original) 6. Authenticity guaranteematerials (1 original).(The content includes: the self-guaranteedeclaration of the authenticity of the declaration materials, andthe false commitment of assuming legal responsibility for thematerials. If the application materials, the specific handlingpersonnel is not the legal representative or the person in charge,the enterprise shall submit the power of attorney The businessscope of the third class medical device license includes: medicalelectronic instruments and equipment, medical opticalinstruments,
