第一類醫(yī)療器械是指，通過常規(guī)管理足以保證其安全性、有效性的醫(yī)療器械。

一類醫(yī)療許可證無需辦理經(jīng)營許可證。如果是生產(chǎn)醫(yī)療器械，則需要到相關部門備案。

二、公司增加二類醫(yī)療器械經(jīng)營范圍

二類醫(yī)療器械備案要求，根據(jù)《醫(yī)療器械監(jiān)督管理條例》凡是從事二類醫(yī)療器械經(jīng)營的單位都需要到所在地設區(qū)的市級食品藥品監(jiān)督管理部門備案，二類醫(yī)療器械是具有中度風險，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、體溫計、心電圖機、腦電圖機、顯微鏡、針灸針、生化分析系統(tǒng)、助聽器、超聲消毒設備、不可吸收縫合線等。

要求：

1.商用性質(zhì)辦公60平，倉儲40平

2.2名醫(yī)學專業(yè)人員為企業(yè)負責人

3.產(chǎn)品經(jīng)營目錄

注：符合以上3點，基本上就可以辦理二類醫(yī)療器械備案

提供材料

1.二類醫(yī)療器械備案申請書

2.營業(yè)執(zhí)照或預先核名通知書

3.法定代表人、企業(yè)負責人、質(zhì)量負責人的身份證明、學歷或者職稱證明復印件

4.經(jīng)營場所、庫房地址的地理位置圖、平面圖、房屋產(chǎn)權證明文件或者租賃協(xié)議(附房屋產(chǎn)權證明文件)復印件 5.產(chǎn)品經(jīng)營目錄表

6.產(chǎn)品合格證書

7.上家購銷合同、進貨渠道

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