經(jīng)營(yíng)企業(yè)要知曉辦理三類醫(yī)療器械經(jīng)營(yíng)許可證需要準(zhǔn)備哪些資料。

(1)提交醫(yī)療器械經(jīng)營(yíng)企業(yè)許可證申請(qǐng)表，法定代表人簽字或加蓋企業(yè)公章；

(2)工商行政管理部門出具的企業(yè)名稱預(yù)核準(zhǔn)證明文件或《營(yíng)業(yè)執(zhí)照》復(fù)印件和校驗(yàn)原件；

(3)企業(yè)質(zhì)量管理負(fù)責(zé)人的身份證、學(xué)歷或者職稱證明復(fù)印件及個(gè)人簡(jiǎn)歷；質(zhì)量管理人員的身份證、學(xué)歷或者職稱證明復(fù)印件；

(4)經(jīng)營(yíng)場(chǎng)所、倉(cāng)庫(kù)的地理位置圖、平面圖（注明面積）、房屋產(chǎn)權(quán)證明或者租賃協(xié)議復(fù)印件；

(5)企業(yè)產(chǎn)品質(zhì)量管理制度文件及儲(chǔ)存設(shè)施、設(shè)備目錄。

(6）對(duì)于辦理三類醫(yī)療器械經(jīng)營(yíng)許可證內(nèi)容包含有需要冷藏的藥品時(shí)，企業(yè)具備的運(yùn)輸裝備、倉(cāng)儲(chǔ)設(shè)施設(shè)備情況表。

、第三類醫(yī)療器械經(jīng)營(yíng)許可證怎么辦理

（1）申請(qǐng)人提交申請(qǐng)資料到相關(guān)部門；

（2）相關(guān)部門受理申請(qǐng)人的申請(qǐng)；

（3）到實(shí)際場(chǎng)地進(jìn)行勘察以及對(duì)產(chǎn)品進(jìn)行審核；

（4）準(zhǔn)予頒發(fā)三類醫(yī)療器械許可證。

二、第三類醫(yī)療器械經(jīng)營(yíng)許可證辦理流程：

1、經(jīng)營(yíng)企業(yè)經(jīng)辦人攜帶上述資料前往監(jiān)督管理部門申請(qǐng)經(jīng)營(yíng)許可；

2、工作人員受理資料，并于30個(gè)工作日內(nèi)進(jìn)行審查，必要時(shí)組織核查；

re for the business license of three types of medical e (1) Submit the application form for the license of the medical device trading enterprise, signed by the legal representative or affix the official seal of the enterprise; (2) A copy of the pre-approval certificate of the enterprise name or the Business License issued by the administrative department for industry and commerce; (3) A copy of the id card, educational background or professional title certificate and personal resume of the management manager of the enterprise; a copy of the ID card, educational background or professional title certificate of the management personnel; (4) The map of the geographical location, the plan (indicating the area), the property right certificate or the copy of the lease agreement; (5) Enterprise product management system documents and catalogue of storage facilities and e (6) Table of transportation e and