器械经营许可证办理方式如下：
（1）申请人提交申请资料到相关部门；
（2）相关部门受理申请人的申请；
（3）到实际场地进行勘察以及对产品进行审核；
（4）准予颁发三类医疗器械许可证。
2、法律依据：《医疗器械监督管理条例》第十四条
第一类医疗器械产品备案和申请第二类、第三类医疗器械产品注册，应当提交下列资料：
（一）产品风险分析资料；
（二）产品技术要求；
（三）产品检验报告；
（四）临床评价资料；
（五）产品说明书以及标签样稿；
（六）与产品研制、生产有关的质量管理体系文件；
（七）证明产品安全、有效所需的其他资料。
追溯。
二、三类医疗器械许可证注册需要什么材料
三类医疗器械许可证注册所需材料如下：
1、企业名称与经营范围，注册资本及股东出资比例，股东等身份证明；
2、医疗器械产品注册证书、供应商营业执照、许可证及授权书；
3、质量管理文件等；
he device business license is handled as follows: (1) Theapplicant shall submit the application materials to the relevantdepartments; (2) Relevant departments shall accept the applicationof the applicant; (3) Investigate the actual site and audit theproducts; (4) Grant the issuance of a class III medical devicelicense. 2. Legal basis: Article 14 of the Regulations on theSupervision and Administration of Medical Devices As for theregistration of Class II and III, the following materials shall besubmitted: (1) Product risk analysis data; (2) Technicalrequirements for the products; (3) Product inspection report; (4)Clinical evaluation data; (5) Product specification and labelsamples; (6) quality management system documents related to productdevelopment and production; (7) other materials required to provethe safety and effectiveness of the product. retrospect. 2. Whatmaterials are required for the registration of the class IIImedical device license The materials required for the licenseregistration of Class III medical devices are as follows: 1.Enterprise name and business scope, registered capital andproportion of shareholder contribution, shareholders and otheridentity certificates; 2. Medical device product registrationcertificate, supplier business license, license and authorizationletter; 3. Quality
