6.產品合格證書

7.上家購銷合同、進貨渠道

注：二類醫療器械備案有效期為長期，到期前6個月到所在地設區的市級食品藥品監督管理部門換發二類醫療器械備案新憑證

三、公司增加三類醫療器械經營范圍

三類醫療器械經營許可證要求：

1、場地要求：必須是辦公性質，使用面積要最少達到60平方米;

2、人員要求：需要有3名相關人員(公司負責人、質量負責人、質量檢查人員)的備案并且持有證書;

3、產品要求：必須要有合乎業務范圍的產品信息，并出具證書;

4、其他相關法律法規要求。

經營三類類醫療器械的，應具備與經營規模相適應的經營場所和庫房

oduct 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 Re for the Business License of Class III Medical Device: 1, site re: must be office nature, the use area of at least 60 square meters; 2. Personnel re: 3 relevant personnel (company responsible person, responsibl