,供應(yīng),商務(wù)服務(wù),公司注冊(cè)服務(wù),國內(nèi)公司注冊(cè)"/> 有效期屆滿需要延續(xù)的,醫(yī)療器械經(jīng)營企業(yè)應(yīng)當(dāng)在有效期屆滿6個(gè)月前,向原發(fā)證部門提出《"/>
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: | 長期有效 |
發(fā)布時(shí)間: | 2023-11-25 04:56 |
最后更新: | 2023-11-25 04:56 |
瀏覽次數(shù): | 52 |
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1、醫(yī)療器械經(jīng)營許可證的有效期只有5年。有效期屆滿需要延續(xù)的,醫(yī)療器械經(jīng)營企業(yè)應(yīng)當(dāng)在有效期屆滿6個(gè)月前,向原發(fā)證部門提出《醫(yī)療器械經(jīng)營許可證》延續(xù)申請(qǐng)。
2、應(yīng)當(dāng)具有符合醫(yī)療器械經(jīng)營質(zhì)量管理要求的計(jì)算機(jī)信息管理系統(tǒng),保證經(jīng)營產(chǎn)品的可追溯。
3、應(yīng)當(dāng)建立銷售記錄制度和建立質(zhì)量管理自查制度。
4、自行停業(yè)一年以上,重新經(jīng)營時(shí),應(yīng)當(dāng)提前書面報(bào)告所在地設(shè)區(qū)的市級(jí)食品藥品監(jiān)督管理部門,經(jīng)核查符合要求后方可恢復(fù)經(jīng)營。
關(guān)于在京辦理三類醫(yī)療器械經(jīng)營許可證的更多問題,歡迎私信小編,
一、三類醫(yī)療器械經(jīng)營許可證如何辦理
1、很多藥品或者醫(yī)療器械的經(jīng)銷商,如果沒有三類醫(yī)療器械經(jīng)營許可證,很多產(chǎn)品就不能賣,比如說體外診斷試劑就屬于三類醫(yī)療器械,只有有相關(guān)證書,才能銷售這種產(chǎn)品。
2、要辦理三類醫(yī)療器械經(jīng)營許可證,必須有相關(guān)的營業(yè)執(zhí)照,一般營業(yè)執(zhí)照上的經(jīng)營范圍這一欄,需要明確寫道可以銷售三類醫(yī)療器械。如果沒有,需要去工商局辦理增項(xiàng)。
3、銷售三類醫(yī)療器械,你必須要自己的庫房,而且?guī)旆坷镄枰O(shè)置冷藏庫,因?yàn)槿愥t(yī)療器械,是有保溫需要的,超過一定的溫度,就容易變質(zhì)影響產(chǎn)品質(zhì)量,所以很少有經(jīng)銷商有銷售三類醫(yī)療器械的資格。
system that meets the re of business management of medical devices to ensure the traceability of business products. 3. A sales record system and a management self-inspection system shall be established. 4. When suspending business for more than one year and re-operating, it shall submit a written report in advance to the food and drug supervisory and administrative department of the city where it is located, and shall resume business only after checking that it meets the re. about more about the third class of medical device business license in Beijing, welcome private messages, how to handle the first and third class of medical device business license 1. Many distributors of drugs or medical devices cannot be sold without the business license of third class medical devices. For example, in vitro diagnostic reagents belong to third class medical devices, and only with releva