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。
2、法律依據(jù)：《醫(yī)療器械監(jiān)督管理條例》第十四條
第一類醫(yī)療器械產(chǎn)品備案和申請第二類、第三類醫(yī)療器械產(chǎn)品注冊，應(yīng)當提交下列資料：
（一）產(chǎn)品風險分析資料；
（二）產(chǎn)品技術(shù)要求；
（三）產(chǎn)品檢驗報告；
（四）臨床評價資料；
（五）產(chǎn)品說明書以及標簽樣稿；
（六）與產(chǎn)品研制、生產(chǎn)有關(guān)的質(zhì)量管理體系文件；1、經(jīng)營企業(yè)提交的《醫(yī)療
醫(yī)療器械經(jīng)營許可證。

醫(yī)療企業(yè)經(jīng)營許可證一共有三類，其中辦理一類醫(yī)療器械許可證可以直接辦理，經(jīng)營二類產(chǎn)品是需要辦理二類醫(yī)療器械經(jīng)營備案憑證，經(jīng)營三類產(chǎn)品則需要辦理三類醫(yī)療器械經(jīng)營許可證。經(jīng)營企業(yè)必須明確申請三類醫(yī)療器械經(jīng)營許可證的條件并滿足相關(guān)要求。（一）具有與經(jīng)營規(guī)模和經(jīng)營范圍相適應(yīng)的質(zhì)量管理機構(gòu)或者質(zhì)量管

on materials to the relevant departments; (2) the relevant departments accept the application of the applicant; (3) investigate the actual site and review the products; (4) grant the issuance of class III medical device license.2. Legal basis: Article 14 of the Regulations on Supervision and Administration of Medical Devices for the filing of Class I medical devices and the application for the registration of Class II and Class III medical devices, the following materials shall be submitted: (1) product risk analysis data; (2) product technical re; (3) product inspection report; (4); (5) clinical evaluation data; product description and label samples; (6) management system documents related to product development and production; 1. Business license of medical and medical devices submitted by the operating enterprise. There are three types of medical enterprise business licenses, among which the first class medical device license can be directly handled, the operation of second class products needs to apply for the record certificate of second class medical devices, and the operation of third class produc