三、公司增加三類醫(yī)療器械經營范圍

三類醫(yī)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(yè)務范圍的產品信息，并出具證書;

4、其他相關法律法規(guī)要求。

經營三類類醫(yī)療器械的，應具備與經營規(guī)模相適應的經營場所和庫房

1.經營類代號為三類-6821醫(yī)用電子儀器設備、三類-6846植入材料人工器官、三類-6863口腔科材料、三類-6877介入器材產品的，經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。

ness License 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 warehouse area shall not be less than 40 square meters. 2. Business cla