三、公司增加三類(lèi)醫療器械經(jīng)營(yíng)范圍

三類(lèi)醫療器械經(jīng)營(yíng)許可證要求：

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

2、人員要求：需要有3名相關(guān)人員(公司負責人、質(zhì)量負責人、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)法律法規要求。

經(jīng)營(yíng)三類(lèi)類(lèi)醫療器械的，應具備與經(jīng)營(yíng)規模相適應的經(jīng)營(yíng)場(chǎng)所和庫房

1.經(jīng)營(yíng)類(lèi)代號為三類(lèi)-6821醫用電子儀器設備、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，庫房使用面積不得少于40平方米。

2.經(jīng)營(yíng)類(lèi)代號為三類(lèi)-6815注射穿刺器械、三類(lèi)-6845體外循環(huán)及液處理設備、三類(lèi)-6864醫用衛生材料及敷料、三類(lèi)-6865醫用縫合材料及粘合劑、三類(lèi)-6866醫用高分子材料及制品的,經(jīng)營(yíng)場(chǎng)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。

3.從事類(lèi)代號為三類(lèi)-6822醫用光學(xué)器具、儀器及內窺鏡設備(jinxian軟性角膜接

son, 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 class code for three-6815 injection puncture instruments, three-6845 extracorporeal circulation and liquid treatment e, three-6864 medical health materials and dressings, three-6865 medical suture materials and adhesives, three-6866 medical polymer materials and products, premises use area of not less than 60 square meters, warehouse use area shall not be less than 80 square meters. 3. Engaged in class III-6822 me