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(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;

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

1.經(jīng)營類代號為三類-6821醫(yī)用電子儀器設(shè)備、三類-6846植入材料人工器官、三類-6863口腔科材料、三類-6877介入器材產(chǎn)品的，經(jīng)營場所使用面積不得少于100平方米，庫房使用面積不得少于40平方米。

2.經(jīng)營類代號為三類-6815注射穿刺器械、三類-6845體外循環(huán)及液處理設(shè)備、三類-6864醫(yī)用衛(wèi)生材料及敷料、三類-6865醫(yī)用縫合材料及粘合劑、三類-6866醫(yī)用高分子材料及制品的,經(jīng)營場所使用面積不得少于60平方米，庫房使用面積不得少于80平方米。

nse of Class III Medical Device: 1, 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 III-6863 stomatology materials, class III-6877 interventional e products, the use area of the business site shall not be less than 100 square meters, and the wareho