二、公司增加二類醫療器械經營范圍

二類醫療器械備案要求，根據《醫療器械監督管理條例》凡是從事二類醫療器械經營的單位都需要到所在地設區的市級食品藥品監督管理部門備案，二類醫療器械是具有中度風險，需要控制管理以保證其安全、有效的醫療器械。如：醫用縫合針、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、助聽器、超聲消毒設備、不可吸收縫合線等。

要求：

1.商用性質辦公60平，倉儲40平

2.2名醫學專業人員為企業負責人

3.產品經營目錄

注：符合以上3點，基本上就可以辦理二類醫療器械備案

提供材料

1.二類醫療器械備案申請書

2.營業執照或預先核名通知書

3.法定代表人、企業負責人、質量負責人的身份證明、學歷或者職稱證明復印件

ope of class II medical devices According to the filing re 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 equipm