北京公司如何辦理增加醫(yī)療器械經(jīng)營范圍呢?增加醫(yī)療器械經(jīng)營范圍有什么要求呢?徐冰為您詳細介紹：

一、公司增加一類醫(yī)療器械經(jīng)營范圍

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(guān)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(shè)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(fēng)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(shè)備、不可吸收縫合線等。

 of medical devices? What are the re for increasing the business scope of medical devices? Next, Xu Bing will introduce it to you in detail: 1. The company has increased the business scope of class I medical devices The first type of medical devices refer to the medical devices that are sufficient to ensure their safety and effectiveness through routine management. Class I medical license does not need for a business license. If it is making medical devices, it needs to be filed with the relevant departments. 2. The company has increased the business scope 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 regulator