北京星期三企业管理咨询有限公司业务部
工商注册 , 资质审批 , 代理记账 , 建委资质 , 舞美资质 , 拍卖资质
朝阳高碑店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,

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。

ope of the three types of medical devices Requirements for the Business License of Class III Medical Device: 1, the site requirements: must be the office nature, the use of the area to reach at least 60 square meters; 2. Personnel requirements: 3 relevant personnel (company responsible person, 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 business scope, and issue a certificate; 4. Other relevant laws and regulations and requirements. For three types of medical devices, it shall have a business site and warehouse suitable with the scale of operation 1. If the business code is class III-6821 medical electronic equipment, Class III-6846 implant materials artificial organs, Class II


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