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西城西四医疗器械三类经营许可证二类备案专业办理快捷包下证

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;

理或者不予核发《医疗器械经营企业许可证》,并给予警告。申请人在1年内不

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

o 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. 2. Legal basis: Article 14 of the Regulations on the Supervision and Administration of Medical Devices As for the registration of Class II and III medical devices, the following materials shall be submitted: (1) Product risk analysis data; (2) Technical requirements for the products; (3) Product inspection report; (4) Clinical evaluation data; (5) Product specification and label samples; (6) quality management system documents related to product development and production; The License of Medical Device Operating Enterprise shall not be issued and given a warning. The applicant is not available within 1 year Procedures for handling the business license of Class III medical devices: 1. Submit the application materials for medical device business license to the Food and Drug Administration; 2. Number of the Food and Drug Administration

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