醫(yī)療器械三類(lèi): | 注冊(cè) |
醫(yī)療器械二類(lèi): | 注冊(cè) |
注冊(cè)公司: | 網(wǎng)絡(luò)銷(xiāo)售備案 |
單價(jià): | 面議 |
發(fā)貨期限: | 自買(mǎi)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: | 2023-11-24 07:03 |
最后更新: | 2023-11-24 07:03 |
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北京公司如何辦理增加醫(yī)療器械經(jīng)營(yíng)范圍呢?增加醫(yī)療器械經(jīng)營(yíng)范圍有什么要求呢?接下來(lái),,徐冰為您詳細(xì)介紹:
一、公司增加一類(lèi)醫(yī)療器械經(jīng)營(yíng)范圍
第一類(lèi)醫(yī)療器械是指,,通過(guò)常規(guī)管理足以保證其安全性,、有效性的醫(yī)療器械。
一類(lèi)醫(yī)療許可證無(wú)需辦理經(jīng)營(yíng)許可證,。如果是生產(chǎn)醫(yī)療器械,,則需要到相關(guān)部門(mén)備案。
二、公司增加二類(lèi)醫(yī)療器械經(jīng)營(yíng)范圍
二類(lèi)醫(yī)療器械備案要求,,根據(jù)《醫(yī)療器械監(jiān)督管理?xiàng)l例》凡是從事二類(lèi)醫(yī)療器械經(jīng)營(yíng)的單位都需要到所在地設(shè)區(qū)的市級(jí)食品藥品監(jiān)督管理部門(mén)備案,,二類(lèi)醫(yī)療器械是具有中度風(fēng)險(xiǎn),需要控制管理以保證其安全,、有效的醫(yī)療器械,。如:醫(yī)用縫合針、血壓計(jì),、體溫計(jì),、心電圖機(jī)、腦電圖機(jī),、顯微鏡,、針灸針、生化分析系統(tǒng),、助聽(tīng)器,、超聲消毒設(shè)備、不可吸收縫合線(xiàn)等,。
scope of medical devices? What are the re for increasing the business scope of medical devices? Next, Xu Bing will introduce it to you in detail: 1. The company has increased the business scope of class I medical devices The first type of medical devices refer to the medical devices that are sufficient to ensure their safety and effectiveness through routine management. Class I medical license does not need for a business license. If it is making medical devices, it needs to be filed with the relevant departments. 2. The company has increased the business scope of class II medical devices According to the filing re of Class II medical devices, accordin