4,、去工商局辦理增項(xiàng),，是需要帶著工商局的工作人員來(lái)查看庫(kù)房的，你zui好把庫(kù)房收拾一下,，然后領(lǐng)取《醫(yī)療器械經(jīng)營(yíng)企業(yè)許可申請(qǐng)表》并填寫(xiě),，并把企業(yè)相關(guān)資質(zhì)全部帶上，還需要帶上質(zhì)量人員的相關(guān)資料,。

5,、三類(lèi)醫(yī)療器械經(jīng)營(yíng)許可證，需要直接去市級(jí)人民政府食品藥品監(jiān)督管理部門(mén)辦理,，在接受資料后的30天內(nèi)進(jìn)行審核,，如果符合相關(guān)規(guī)定，就可以頒發(fā)三類(lèi)醫(yī)療器械經(jīng)營(yíng)許可證,。

二,、經(jīng)營(yíng)許可證是營(yíng)業(yè)執(zhí)照嗎

二者不能等同,。

根據(jù)法律規(guī)定，營(yíng)業(yè)執(zhí)照是法律主體進(jìn)行市場(chǎng)交易主體資格的法定證明,，目前有法人類(lèi)營(yíng)業(yè)執(zhí)照,、個(gè)人獨(dú)資企業(yè)營(yíng)業(yè)執(zhí)照、合伙企業(yè)營(yíng)業(yè)執(zhí)照和個(gè)體工商戶(hù)營(yíng)業(yè)執(zhí)照等,；營(yíng)業(yè)執(zhí)照由工商局頒發(fā),，每年年檢。而經(jīng)營(yíng)許可證,，是法律規(guī)定的某些行業(yè)必須經(jīng)過(guò)許可,，而由主管部門(mén)辦法的許可經(jīng)營(yíng)的證明，如煙草專(zhuān)賣(mài)許可等,。營(yíng)業(yè)執(zhí)照是每個(gè)開(kāi)門(mén)做生意的經(jīng)營(yíng)者都需要辦理的證件,，沒(méi)有這個(gè)證件，就是無(wú)照經(jīng)營(yíng)行為,，是違法的,。經(jīng)營(yíng)許可證是做某種方面的生意所必須取得的證件，這個(gè)證件必須在辦理營(yíng)業(yè)執(zhí)照之前取得,，也就是所謂的前置許可審批文件,，例如賣(mài)

mercial Bureau for additional items, is the need to take the staff of the industrial and commercial bureau to check the warehouse, you would like to clean up the warehouse, and then get the "medical device business enterprise license application form" and fill in, and bring all the relevant of the enterprise, but also need to bring the relevant information of personnel. 5. The business license of Class III medical devices needs to be handled directly by the food and drug supervision and administration department of the municipal people's government, and shall be reviewed within 30 days after receiving the materials. If the relevant regulations are met, the business license of Class III medical device