03.

三類——國家藥監局辦理醫療器械許可證 第三類醫療器械是具有較高風險，需要采取特別措施嚴格控制管理以保證其安全有效的醫療器械，比如常見的輸液器、注射器、靜脈留置針、心臟支架、呼吸機、CT、核磁共振等，其產品和生產經營活動分別由、省級食品藥品監管部門和設區的市食品藥品監管部門實行許可管理，分別發給《醫療器械注冊證》、《醫療器械生產許可證》、《醫療器械經營許可證》。

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

一、公司增加一類醫療器械經營范圍

第一類醫療器械是指，通過常規管理足以保證其安全性、有效性的醫療器械。

一類醫療許可證無需辦理經營許可證。如果是生產醫療器械，則需要到相關部門備案。

二、公司增加二類醫療器械經營范圍

 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 the manufacturer is a medical device, it needs to file with the relevant departments. 2. The company has increased the business scope of class II medical devices