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

一、公司增加一類(lèi)醫療器械經(jīng)營(yíng)范圍

第一類(lèi)醫療器械是指，通過(guò)常規管理足以保證其安全性、有效性的醫療器械。

一類(lèi)醫療許可證無(wú)需辦理經(jīng)營(yíng)許可證。如果是生產(chǎn)醫療器械，則需要到相關(guān)部門(mén)備案。

二、公司增加二類(lèi)醫療器械經(jīng)營(yíng)范圍

二類(lèi)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(lèi)醫療器械經(jīng)營(yíng)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(mén)備案，二類(lèi)醫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(tīng)器、超聲消毒設備、不可吸收縫合線(xiàn)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