首先,要根据规定明确产品的分类,选择符合规范的产品名称和用途。然后,需要获取医疗器械二三类产品的技术评估报告和公告批件,提供相关资料完成注册申请并进行后续审批程序。在整个流程中,我们会提供全程咨询服务,协助您完成所有相关工作。
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《医疗器械经营许可证》属于后置审批
可先办理营业执照
再领取先照后证通知书
再申请办理三类医疗许可
证书有效期为5年
医疗器械经营许可证
01医疗器械经营许可证分类
the registration application and conduct follow-up approval procedures. In the whole process, we will provide full consulting services to assist you with all the related work. Our service is fast, cheap, and very professional. We are well aware of the needs and hardships of enterprises in the medical device qualification registration process. Therefore, we have always been committed to providing quality service for enterprises, with the fastest time, the best quality service, the most economical price for the enterprise to solve the troubles. If you need to register the medical device Class II qualification, you might as well contact us to provide you with first-class consultin