三、第三类医疗器械经营许可证办理所需材料:
1、企业名称与经营范围，注册资本及股东出资比例，股东等sfz明；
2、医疗器械产品注册证书、供应商营业执照、许可证及授权书；
3、质量管理文件等；
4、2个或以上医学专业或相关专业人员证书、sfz明与简历；
5、符合医疗器械经营要求的办公场地及仓库证明；
6、公司章程、股东会决议等；
7、财务人员sfz和上岗证；
8、其它相关材料。
医疗器械是一种用于预防、诊断、治疗或缓解疾病或残疾的工具、设备、仪器或机器。它们包括各种医用产品，如手术器械、医用材料、注射器、心脏起搏器、医疗椅等等。医疗器械行业的发展与医疗技术的进步紧密相关。随着科学技术的不断发展和医学水平的提高，医疗器械的种类和数量也在不断增加。
business license of Class III medical devices: 1, the enterprisename and business scope, the registered capital and the proportionof shareholder contribution, shareholders and other sfz Ming; 2.Medical device product registration certificate, supplier businesslicense, license and authorization letter; 3. Quality managementdocuments, etc.; 4,2 or more medical professional or relatedprofessional certificates, sfz Ming and resume; 5. Office space andwarehouse certificate that meet the business requirements ofmedical equipment; 6. Articles of association, resolutions ofshareholders' meeting, etc.; 7, financial personnel sfz and workcertificate; 8. Other related materials. A medical device is atool, device, instrument, or machine used for the prevention,diagnosis, treatment, or mitigation of illness or disability. Theyinclude a variety of medical products such as surgical instruments,medical materials, syringes, pacemakers, medical chairs and more.The development of the medical device industry is closely relatedto the progress of medical technology. With the continuousdevelopment of science and tec
