| 醫(yī)療器械三類： | 注冊(cè) |
| 醫(yī)療器械二類： | 注冊(cè) |
| 注冊(cè)公司： | 網(wǎng)絡(luò)銷售備案 |
| 單價(jià)： | 面議 |
| 發(fā)貨期限： | 自買家付款之日起 天內(nèi)發(fā)貨 |
| 所在地： | 直轄市 北京 北京海淀 |
| 有效期至： | 長(zhǎng)期有效 |
| 發(fā)布時(shí)間： | 2023-11-25 04:41 |
| 最后更新： | 2023-11-25 04:41 |
| 瀏覽次數(shù)： | 178 |
| 采購(gòu)咨詢： |
請(qǐng)賣家聯(lián)系我
|
4.經(jīng)營(yíng)場(chǎng)所、庫(kù)房地址的地理位置圖、平面圖、房屋產(chǎn)權(quán)證明文件或者租賃協(xié)議(附房屋產(chǎn)權(quán)證明文件)復(fù)印件 5.產(chǎn)品經(jīng)營(yíng)目錄表
6.產(chǎn)品合格證書(shū)
7.上家購(gòu)銷合同、進(jìn)貨渠道
注：二類醫(yī)療器械備案有效期為長(zhǎng)期，到期前6個(gè)月到所在地設(shè)區(qū)的市級(jí)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(yíng)范圍
三類醫(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);
map, floor plan, house property right certificate or lease agreement (attached with the house property right certificate). 5 6. Product certificate 7. Last home purchase and sales contract and purchase channels Note: The record validity period of class II medical devices is long-term, and the new record certificate of Class II medical devices shall be issued to the municipal food and drug regulatory department 6 months before the expiration 3. The company has increased the business scope of the three types of medical devices Re for the Business License of Class III Medical Device: 1, site re: must be office nature, the use area of at least 60 square meters; 2. Personnel re: 3 relevant personnel (company respons
