三類(lèi)醫療器械指的是植入人體，用于支持、維持生命，對人體具有潛在危險，對其安全性、有效性必須嚴格控制的醫療器械?，F行制度規范下，經(jīng)營(yíng)三類(lèi)醫療器械的經(jīng)營(yíng)主體需要按程序辦理三類(lèi)醫療器械經(jīng)營(yíng)許可證。

那么在北京如何辦理三類(lèi)醫療經(jīng)營(yíng)許可證，辦理許可證又有哪些條件及流程，小編今天帶著(zhù)滿(mǎn)滿(mǎn)的干貨知識與您分享。

三類(lèi)醫療器械常見(jiàn)產(chǎn)品有哪些：

植入式心臟起搏器、體外震波碎石機、病人有創(chuàng )監護系統、人工晶體、有創(chuàng )內窺鏡、超聲手術(shù)刀、彩色超聲成像設備、激光手術(shù)設備、高頻電刀、微波緩解儀、醫用核磁共振成像設備、X線(xiàn)緩解設備、醫用高能設備、人工心肺機、內固定器材、人工心臟瓣膜、人工腎、呼吸麻醉設備、一次性使用無(wú)菌注射器、一次性使用輸液器、輸血器、CT等。

三類(lèi)申請醫療器械經(jīng)營(yíng)許可證條件：

1.具有與經(jīng)營(yíng)規模和經(jīng)營(yíng)范圍相適應的質(zhì)量管理機構或者專(zhuān)職質(zhì)量管理人員。質(zhì)量管理人員應當具有國家認可的相關(guān)專(zhuān)業(yè)學(xué)歷或者職稱(chēng)；

2.具有與經(jīng)營(yíng)規模和經(jīng)營(yíng)范圍相適應的相對獨立的經(jīng)營(yíng)場(chǎng)所；

3.具有與經(jīng)營(yíng)規模和經(jīng)營(yíng)范圍相適應的儲存條件，包括具有符合醫療器械產(chǎn)品特性要求的儲存設施、設備；

4.應當建立健全產(chǎn)品質(zhì)量管理制度，包括采購、進(jìn)貨驗收、倉儲保管、出庫復核、質(zhì)量跟蹤和不良事件的報告制度等；

 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 procedures. So in Beijing how to apply for the three types of medical business license in Beijing, what are the conditions and procedures for the license, Xiaobian today with full of dry knowledge to share with you. What are the common products of Class III medical devices: Implantable cardiac pacemaker, external shock wave lithotripsy machine, patient invasive monitoring system, artificial lens, invasive endoscope, ultrasonic scalpel, color ultrasound imaging e, laser surgery e, high frequency electric knife, microwave relief instrument, medical nuclear magnetic resonance imaging e, X-ray relief e, medical high-energy e, artificial heart-lung machine, internal fixation e, artificial