醫療器械三類(lèi): | 注冊 |
醫療器械二類(lèi): | 注冊 |
注冊公司: | 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 天內發(fā)貨 |
所在地: | 直轄市 北京 北京海淀 |
有效期至: | 長(cháng)期有效 |
發(fā)布時(shí)間: | 2023-11-25 06:55 |
最后更新: | 2023-11-25 06:55 |
瀏覽次數: | 106 |
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二類(lèi)——市藥監局辦理醫療器械經(jīng)營(yíng)備案 第二類(lèi)醫療器械是具有中度風(fēng)險,需要嚴格控制管理以保證其安全有效的醫療器械,比如我們日常生活中常見(jiàn)的創(chuàng )可貼、避孕套、體溫計、血壓計、制氧機、霧化器等,其產(chǎn)品和生產(chǎn)活動(dòng)由省級食品藥品監管部門(mén)實(shí)行許可管理,分別發(fā)給《醫療器械注冊證》和《醫療器械生產(chǎn)許可證》。經(jīng)營(yíng)活動(dòng)由設區的市級食品藥品監管部門(mén)實(shí)行備案管理;
03.
三類(lèi)——國家藥監局辦理醫療器械許可證 第三類(lèi)醫療器械是具有較高風(fēng)險,需要采取特別措施嚴格控制管理以保證其安全有效的醫療器械,比如常見(jiàn)的輸液器、注射器、靜脈留置針、心臟支架、呼吸機、CT、核磁共振等,其產(chǎn)品和生產(chǎn)經(jīng)營(yíng)活動(dòng)分別由、省級食品藥品監管部門(mén)和設區的市食品藥品監管部門(mén)實(shí)行許可管理,分別發(fā)給《醫療器械注冊證》、《醫療器械生產(chǎn)許可證》、《醫療器械經(jīng)營(yíng)許可證》。
北京公司如何辦理增加醫療器械經(jīng)營(yíng)范圍呢?增加醫療器械經(jīng)營(yíng)范圍有什么要求呢?徐冰為您詳細介紹:
ol management to ensure its safe and effective medical devices, such as our daily life, band, condoms, thermometer, blood monitor, oxygen generator, atomizer, its products and production activities by the provincial food and drug regulatory department licensing management, respectively issued to the medical device registration certificate and medical device production license. Business activities shall be put on record by the food and drug regulatory departments of the city divided into districts; 03. Three —— state food and drug administration license the third category of medical devices is a high risk, take special measures to strictly control and management to ensure its safe and effective medical devices, such as common infusion, syringe, intravenous needle, heart stent, ventilator, CT, NMR, etc., its products and production and business activitie