6.產(chǎn)品合格證書

7.上家購銷合同,、進貨渠道

注：二類醫(yī)療器械備案有效期為長期,，到期前6個月到所在地設(shè)區(qū)的市級食品藥品監(jiān)督管理部門換發(fā)二類醫(yī)療器械備案新憑證

三、公司增加三類醫(yī)療器械經(jīng)營范圍

三類醫(yī)療器械經(jīng)營許可證要求：

1,、場地要求：必須是辦公性質(zhì),，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(guān)人員(公司負責(zé)人、質(zhì)量負責(zé)人,、質(zhì)量檢查人員)的備案并且持有證書;

3,、產(chǎn)品要求：必須要有合乎業(yè)務(wù)范圍的產(chǎn)品信息，并出具證書;

4,、其他相關(guān)法律法規(guī)要求,。

經(jīng)營三類類醫(yī)療器械的，應(yīng)具備與經(jīng)營規(guī)模相適應(yīng)的經(jīng)營場所和庫房

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 in accordance with the business scope, and issue a certificate; 4. Other relevant laws and regulation re. For three types of medical devices, it shall have a business site and warehouse suitable with the scale of operation