朝阳和平街北京医疗器械二类备案医疗器械三类经营许可证专业办理经验丰富安全速度快可靠

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。

三类医疗器械经营许可证办理所需大致资料:

1、企业经营执照;2、企业负责人以及质检人员和技术人员的身份、学历、职称证明;3、经营场所证明以及地理位置图。

三类医疗器械经营许可证办理之后需要明确的几个注意事项

1、医疗器械经营许可证的有效期只有5年。有效期届满需要延续的，医疗器械经营企业应当在有效期届满6个月前，向原发证部门提出《医疗器械经营许可证》延续申请。

ty guarantee materials (1 original).(The content includes: theself-guarantee declaration of the authenticity of the declarationmaterials, and the false commitment of assuming legalresponsibility for the materials. If the application materials, thespecific handling personnel is not the legal representative or theperson in charge, the enterprise shall submit the power of attorneyThe business scope of the third class medical device licenseincludes: medical electronic instruments and equipment, medicaloptical instruments, instruments and endoscope equipment, medicalmagnetic resonance equipment, medical X-ray equipment, operatingroom, emergency room, medical room equipment and equipment. Thesale of medical devices must be applied for the business licenseCertificate, according to the relevant laws and regulations,the