我公司主要经营代办北京医疗器械公司注册|代办北京三类医疗器械公司注册|代办北京二类医疗器械备案凭证|代办北京食品经营许可证|代办北京医疗器械网络备案|代办北京辐射安全许可等资质专项审批服务

三类医疗器械指的是植入人体，用于支持、维持生命，对人体具有潜在危险，对其安全性、有效性必须严格控制的医疗器械。现行制度规范下，经营三类医疗器械的经营主体需要按程序办理三类医疗器械经营许可证。

那么在北京如何办理三类医疗经营许可证，办理许可证又有哪些条件及流程，小编今天带着满满的干货知识与您分享。

三类医疗器械常见产品有哪些：

植入式心脏起搏器、体外震波碎石机、病人有创监护系统、人工晶体、有创内窥镜、超声手术刀、彩色超声成像设备、激光手术设备、高频电刀、微波缓解仪、医用核磁共振成像设备、X线缓解设备、医用高能设备、人工心肺机、内固定器材、人工心脏瓣膜、人工肾、呼吸麻醉设备、一次性使用无菌注射器、一次性使用输液器、输血器、CT等。

三类申请医疗器械经营许可证条件：

ing class medical equipment for the record certificate | Beijing food business license | Beijing medical equipment network for the record | Beijing radiation safety license qualification special examination and approval services Class III medical devices refer to the medical devices implanted in human body to support and maintain life, with potential danger to human body, and their safety and effectiveness must be strictly controlled. Under the current system and norms, the business entities of third class medical devices need to apply for the business license of third class medical devices according to the procedur