三類醫(yī)療器械經(jīng)營許可證如何辦理
1、三類醫(yī)療器械經(jīng)營許可證辦理方式如下：
（1）申請人提交申請資料到相關(guān)部門；
（2）相關(guān)部門受理申請人的申請；
（3）到實際場地進行勘察以及對產(chǎn)品進行審核；
（4）準予頒發(fā)三類醫(yī)療器械許可證。

三類醫(yī)療器械作為目前醫(yī)療器械分類中危險性最高的品類，嚴格受到相關(guān)部門的監(jiān)督和管理，對于很多經(jīng)營三類醫(yī)療器械的家人們來說，很多基礎(chǔ)性問題還不能完全掌握，今天我們就來看一看，三類醫(yī)療器械經(jīng)營范圍有哪些？又該如何申請三類醫(yī)療器械經(jīng)營許可證！

handle the business license of class III medical devices
1. The business license of Class III medical devices is handled as follows:
(1) The applicant shall submit the application materials to the relevant departments;
(2) Relevant departments shall accept the application of the applicant;
(3) Investigate the actual site and audit the products;
(4) Grant the issuance of a class III medical device license.

Three kinds of medical devices as the highest risk in the medical device classification category, strictly by the supervision and management, but for many families of three kinds of medical devices, many basic problems is not fully grasp, today we will take a look, what are three business scope of medical devices? How to apply for the three types of medical e business license again!

平面圖（注明面積）和與被委托方簽署的書面協(xié)議復(fù)印件、被委托方的《醫(yī)療器械經(jīng)營許可證》復(fù)印件） 6．經(jīng)營設(shè)施、設(shè)備目錄； 7．經(jīng)營質(zhì)量管理制度、工作程序等文件目錄； 8．計算機信息管理系統(tǒng)基本情況介紹和功能說明； 9．凡申請企業(yè)申報材料時，具體辦理人員不是法定代表人或負責(zé)人本人，企業(yè)應(yīng)當提交《 授權(quán)委托書》；10．申報材料真實性自我保證聲明，并對材料作出如有虛假承擔(dān)法律責(zé)任的承諾。