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。

要求：

1.商用性質(zhì)辦公60平，倉(cāng)儲(chǔ)40平

2.2名醫(yī)學(xué)專(zhuān)業(yè)人員為企業(yè)負(fù)責(zé)人

3.產(chǎn)品經(jīng)營(yíng)目錄

注：符合以上3點(diǎn)，基本上就可以辦理二類(lèi)醫(yī)療器械備案

提供材料

1.二類(lèi)醫(yī)療器械備案申請(qǐng)書(shū)

2.營(yíng)業(yè)執(zhí)照或預(yù)先核名通知書(shū)

3.法定代表人、企業(yè)負(fù)責(zé)人、質(zhì)量負(fù)責(zé)人的身份證明、學(xué)歷或者職稱(chēng)證明復(fù)印件

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(xiāo)合同、進(jìn)貨渠道

rements of Class II medical devices, according to the Regulations on the Supervision and Administration of Medical Devices, all units engaged in the business of Class II medical devices need to file with the food and drug regulatory department of the city divided into districts. Class II medical devices have moderate risks and need to be controlled and managed to ensure their safe and effective medical devices. Such as: medical suture needle, sphygmomanometer, thermometer, electrocardiogram machine, electroencephalography machine, microscope, acupuncture needle, biochemical analysis system, hearing aid, ultrasonic disinfection e, non-absorbable sutures, etc. ask: 1. Commercial nature of the office 60 square, storage 40 square 2.2 medical professionals are the leaders of the enterprise 3. Product management catalogue Note: To meet the above 3 points, basically can handle