顺义光明北京医疗器械三类经营许可证，医疗器械二类备案提供进销存软件库房速度快专业方便，

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;

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。

以上就是对三类医疗器械经营许可证办理的相关介绍，办理的程序可能较为繁琐。

re, the use area should be less than 45 square meters; 2.Personnel requirements: 3 relevant personnel (company responsibleperson, quality responsible person, quality inspection personnel)need to record and hold the certificate; 3, product requirements:must have the product information in accordance with the businessscope, and issue a certificate; 4. Other relevant laws andregulations and requirements. 3. Procedures for obtaining the ClassIII Medical Device License: 1. The applicant shall submit theapplication materials to the relevant departments; 2. Relevantdepartments shall accept the application of the applicant; 3.Investigate the actual site and audit the products; 4. Grant theissuance of a class III medical device license. The above isthe