无菌医疗器械注册审评中对灭菌资料探讨

      Discussion on the Sterilization Material in the Registration Evaluation of Sterile Medical Device

      • 摘要: 该文首先简单介绍了无菌医疗器械注册审评时灭菌资料的法规要求,其次选取采用多种灭菌方式的软组织过线器套件作为示例产品进行探讨,期望能够为医疗器械注册申请人准备注册资料和技术审评人员进行技术审评提供参考。

         

        Abstract: This article first introduces the regulation requirements for sterilization material in the registration evaluation of sterile medical devices. Secondly, the article chooses the suture passer set kit with multiple sterilization methods as an example product for technical evaluation. The article hopes to provide a reference for the applicant who prepare the registration material and the technical evaluators how to make the evaluation for the medical device registration.

         

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