东城东四十条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靠谱周期短Zui快7天下证

4、2个或以上医学專业或相关專业人员证书、身份证明与简历;

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、财务人员身份证和上岗证;

8、其它相道关材料。

二、办理三回类医疗器械许可证的要求：

1、场地要求：必须是办公性质，使用面积要少达到45平方米;

2、人员要求：需要有3名相关人员(公司负责人、质量负责人、质量检查人员)的备案并且持有证书;

3、产品要求：必须要有合乎业务范围的产品信息，并出具证书;

4、其他相关法律法规要求。

三、办理三类医疗器械许可证的流程：

1、申请人提交申请资料到相关部门;

ertificate and resume of medical professionals or relatedprofessionals; 5. Office space and warehouse certificate that meetthe business requirements of medical equipment; 6. Articles ofassociation, resolutions of shareholders' meeting, etc.; 7. ID cardand post card of financial personnel; 8, other phase channelclearance materials. 2. Requirements for three-of medical devicelicense: 1, site requirements: must be office nature, the use areashould be less than 45 square meters; 2. Personnel requirements: 3relevant personnel (company responsible person, quality responsibleperson, quality inspection personnel) need to record and hold thecertificate; 3, product requirements: must have the productinformation in accordance with the business scope, and issue acertificate; 4.