隨著國民經(jīng)濟的穩(wěn)步發(fā)展和人們對醫(yī)療健康的廣泛關注，醫(yī)療行業(yè)成為眾多投資伙伴關注的焦點。想要涉足醫(yī)療器械領域，這些基礎知識是不能忽視的！

在我國經(jīng)營銷售醫(yī)療器械必須取得相關資質，那么北京地區(qū)三類醫(yī)療器械經(jīng)營許可證如何辦理，今天我們一起學習一下吧！

經(jīng)營范圍包括哪些？

第三類醫(yī)療器械許可的經(jīng)營范圍包括：醫(yī)用電子設備、醫(yī)用光學設備、儀器和內(nèi)鏡設備、醫(yī)用磁共振設備、醫(yī)用X射線設備、手術室、急診室和診室的設備和器具。根據(jù)售賣醫(yī)療器械必須辦理經(jīng)營許可證，,國家相關法律法規(guī)，美國食品藥品監(jiān)督管理局逐步推行醫(yī)療器械管理質量標準化管理體系。醫(yī)療器械經(jīng)營質量管理規(guī)范由國家美國食品藥品監(jiān)督管理局制定。

許可證的辦理條件

根據(jù)《醫(yī)療器械監(jiān)督管理條例》第三十一條的規(guī)定，從事第三類醫(yī)療器械業(yè)務的，經(jīng)營企業(yè)應當向所在地設區(qū)的市級人民政府食品藥品監(jiān)督管理部門申請經(jīng)營許可。

e field of medical devices, these basic knowledge cannot be ignored! In our country, the sales of medical e must obtain relevant , so Beijing area three types of medical e business license how to handle, today we learn it together! What does the business scope include? The business scope of category III medical device license includes: medical electronic e, medical optical e, instruments and endoscopic e, medical magnetic resonance e, medical X-ray e, e and e in the operating room, emergency room and consulting room. According to the sale of medical devices must apply for the business license, the relevant national laws and regulations, the US Food and Drug Administration gradually implement the medical device management standardized management system. The management standards for medical devices are formulated by the United States Food and Drug Administration. Conditions for handling the permit Ac