要根據規(guī)定明確產品的分類，選擇符合規(guī)范的產品名稱和用途。需要獲取醫(yī)療器械二三類產品的技術評估報告和公告批件，提供相關資料完成注冊申請并進行后續(xù)審批程序。在整個流程中，我們會提供全程咨詢服務，協助您完成所有相關工作。

我們的服務快速、便宜且專業(yè)。我們非常了解企業(yè)在醫(yī)療器械資質注冊過程中的需求和苦處。我們始終致力于為企業(yè)提供優(yōu)質的服務，以最快速的時間、最優(yōu)質的服務、最經濟的價格為企業(yè)解決煩惱。如果您需要注冊醫(yī)療器械二三類資質，不妨聯系我們，為您提供yiliu的咨詢服務，快速解決您所有的醫(yī)療器械注冊問題。

《醫(yī)療器械經營許可證》屬于后置審批

可先辦理營業(yè)執(zhí)照

再領取先照后證通知書

再申請辦理三類醫(yī)療許可

證書有效期為5年

醫(yī)療器械經營許可證

01醫(yī)療器械經營許可證分類

the registration application and conduct follow-up approval procedures. In the whole process, we will provide full consulting services to assist you with all the related work. Our service is fast, cheap, and very professional. We are well aware of the needs and hardships of enterprises in the medical device registration process. Therefore, we have always been committed to providing service for enterprises, with the fastest time, the best service, the most economical price for the enterprise to solve the troubles. If you need to register the medical device Class II , you might as well contact us to provide you with first-class consultin