三,、公司增加三類(lèi)醫(yī)療器械經(jīng)營(yíng)范圍

三類(lèi)醫(yī)療器械經(jīng)營(yíng)許可證要求：

1,、場(chǎng)地要求：必須是辦公性質(zhì)，使用面積要最少達(dá)到60平方米;

2,、人員要求：需要有3名相關(guān)人員(公司負(fù)責(zé)人、質(zhì)量負(fù)責(zé)人,、質(zhì)量檢查人員)的備案并且持有證書(shū);

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(shū);

4,、其他相關(guān)法律法規(guī)要求,。

經(jīng)營(yíng)三類(lèi)類(lèi)醫(yī)療器械的,，應(yīng)具備與經(jīng)營(yíng)規(guī)模相適應(yīng)的經(jīng)營(yíng)場(chǎng)所和庫(kù)房

1.經(jīng)營(yíng)類(lèi)代號(hào)為三類(lèi)-6821醫(yī)用電子儀器設(shè)備、三類(lèi)-6846植入材料人工器官,、三類(lèi)-6863口腔科材料,、三類(lèi)-6877介入器材產(chǎn)品的，經(jīng)營(yíng)場(chǎng)所使用面積不得少于100平方米,，庫(kù)房使用面積不得少于40平方米,。

ope of the three types of medical devices Re for the Business License of Class III Medical Device: 1, the site re: must be the office nature, the use of the area to reach at least 60 square 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 in accordance with the business scope, and issue a certificate; 4. Other relevant laws and regulations and re. 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 e, Class III-6846 implant materials artificial organs, Class II