三、公司增加三类医疗器械经营范围
三类医疗器械经营许可证要求：
1、场地要求：必须是办公性质，使用面积要Zui少达到60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。
经营三类类医疗器械的，应具备与经营规模相适应的经营场所和库房
1.经营类代号为三类-6821医用电子仪器设备、三类-6846植入材料人工器官、三类-6863口腔科材料、三类-6877介入器材产品的，经营场所使用面积不得少于100平方米，库房使用面积不得少于40平方米。
ss scope of the three types of medical devices Re forthe Business License of Class III Medical Device: 1, sitere: must be office nature, the use area of at least 60square meters; 2. Personnel re: 3 relevant personnel(company responsible person, responsible person, inspection personnel) need to record and hold the certificate; 3,product re: must have the product information inaccordance with the business scope, and issue a certificate; 4.Other relevant laws and regulation re. For three types ofmedical devices, it shall have a business site and warehousesuitable with the scale of operation 1. If the business code isclass III-6821 medical electronic e, Class III-6846 implantmaterials artificial organs, Class III-6863 stomatologymaterials,
