鏡,、超聲手術(shù)刀,、彩色超聲成像設(shè)備,、激光手術(shù)設(shè)備、高頻電刀,、微波緩解儀、醫(yī)用核磁共振成像設(shè)備,、X線緩解設(shè)備,、醫(yī)用高能設(shè)備、人工心肺機(jī),、內(nèi)固定器材,、人工心臟瓣膜、人工腎,、呼吸麻醉設(shè)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,。

三類申請(qǐng)醫(yī)療器械經(jīng)營(yíng)許可證條件：

1.具有與經(jīng)營(yíng)規(guī)模和經(jīng)營(yíng)范圍相適應(yīng)的質(zhì)量管理機(jī)構(gòu)或者專職質(zhì)量管理人員。質(zhì)量管理人員應(yīng)當(dāng)具有國(guó)家認(rèn)可的相關(guān)專業(yè)學(xué)歷或者職稱,；

2.具有與經(jīng)營(yíng)規(guī)模和經(jīng)營(yíng)范圍相適應(yīng)的相對(duì)獨(dú)立的經(jīng)營(yíng)場(chǎng)所,；

3.具有與經(jīng)營(yíng)規(guī)模和經(jīng)營(yíng)范圍相適應(yīng)的儲(chǔ)存條件，包括具有符合醫(yī)療器械產(chǎn)品特性要求的儲(chǔ)存設(shè)施,、設(shè)備,；

4.應(yīng)當(dāng)建立健全產(chǎn)品質(zhì)量管理制度，包括采購(gòu),、進(jìn)貨驗(yàn)收,、倉(cāng)儲(chǔ)保管、出庫(kù)復(fù)核,、

nized by the state; 2. Having a relatively independent business site commensurate with the scale and scope of business; 3. Having storage conditions suitable with the scale and scope of business, including storage facilities and e that meet the re of the characteristics of medical device products; 4. The product management system shall be established and improved, including procurement, purchase and acceptance, warehousing, warehousing and review, and