、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(jìn)行勘察以及對產(chǎn)品進(jìn)行審核；
（4）準(zhǔn)予頒發(fā)三類醫(yī)療器械許可證,。
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(dāng)提交下列資料：
（一）產(chǎn)品風(fēng)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(biāo)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,。首先,，經(jīng)營企業(yè)必須明確申請三

ess license of Class III medical devices are as follows: (1) the applicant submits the application 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 the 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 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 la