經(jīng)營的單位都需要到所在地設(shè)區(qū)的市級(jí)食品藥品監(jiān)督管理部門備案，二類醫(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)、助聽器、超聲消毒設(shè)備、不可吸收縫合線等。

要求：

1.商用性質(zhì)辦公60平，倉儲(chǔ)40平

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

3.產(chǎn)品經(jīng)營目錄

注：符合以上3點(diǎn)，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(yù)先核名通知書

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)歷或者職稱證明復(fù)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(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)營目錄表

6.產(chǎn)品合格證書

ercial office 60 square, storage 40 square 2.2 medical professionals are the leaders of the enterprise 3. Product management catalogue Note: If the line of the above 3 points, basically can handle the record of class II medical devices Provide materials 1. Application for filing of Class II medical devices 2. Business license or pre-check name notice 3. Copy of the identity certificate, education background or professional title certificate of the legal representative, the person in charge of the enterprise and the person in charge of 4. Copy of the geographical location map, floor plan, house