(1) the applicant shall submit the application materials to therelevant departments; (2) the relevant departments shall accept theapplication of the applicant; (3) investigate the actual site andreview the products; (4) grant the issuance of the third IIImedical device license.2. Legal basis: Article 14 of theRegulations on the Supervision and Administration of MedicalDevices for the filing of Class I medical devices and theapplication for the registration of Class II and Class III medicaldevices, The following materials shall be submitted: (1) productrisk analysis data; (2) technical requirements of the product; (3)product inspection report; (4) clinical evaluation data; (5)product specification and label samples; 1. Prepare a copy of thelicense, Where the applicant obtains the Medical Device OperatingEnterprise License by cheating or bribery, The (food) and drugregulatory department shall revoke its Medical Device TradingEnterprise License, Give a warning, And shall be fined not lessthan 10,000 yuan but not more than 20,000 yuan. The applicant shallnot apply for the Medical Device Business Enterprise License againwithin 3 years. Procedures for handling the business license ofClass III medical devices: 1. Submit application materials formedical
（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；医疗器械二类备案流程：1、准备执照副本，申请人以欺骗、贿赂等不正当手段取得《医疗器械经营企业许可证》的，（食品）药品监督管理部门应当撤销其《医疗器械经营企业许可证》，给予警告，并处1万元以上2万元以下罚款。申请人在3年内不得申请《医疗器械经营企业许可证》。办理三类医疗器械经营许可证的办理流程：
1.向食品药品监督管理局提交医疗器械经营许可证申请材料；
2.食品药品监督管理局数据形式审查；
3.数据正式受理；
4.有关部门的行政审查
