西城新街口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，

提供材料

1.二类医疗器械备案申请书

2.营业执照或预先核名通知书

3.法定代表人、企业负责人、质量负责人的身份证明、学历或者职称证明复印件

4.经营场所、库房地址的地理位置图、平面图、房屋产权证明文件或者租赁协议(附房屋产权证明文件)复印件 5.产品经营目录表

6.产品合格证书

7.上家购销合同、进货渠道

注：二类医疗器械备案有效期为长期，到期前6个月到所在地设区的市级食品药品监督管理部门换发二类医疗器械备案新凭证

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

tificate, education background or professional title certificate of the legal representative, the person in charge of the enterprise and the person in charge of quality 4. Copy of the geographical location map, floor plan, house property right certificate or lease agreement (attached with the house property right certificate). 5 6. Product qualification certificate 7. Last home purchase and sales contract and purchase channels Note: The record validity period of class II medical devices is long-term, and the new record certificate of Class II medical devices shall be issued to the municipal food and drug regulatory department 6 months before the expiration 3. The company has increased the business scope of the three types of medical devices Requirements for the Business License of Class III Medical Device: 1, site requirements: must be office nature, the us