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为配合国家医药管理局发布的《医疗器械新产品管理暂行办法》的贯彻实施,进一步搞好清理整顿工作,保证医疗器械产品使用的安全有效,国家医药管理局决定对全国医疗器械在产产品的鉴定情况进行登记。
In line with the implementation of the “Provisional Measures for the Management of New Medical Device Products” promulgated by the State Administration of Pharmaceuticals, we will continue to do a good job of cleaning up and rectifying medical products to ensure the safe and effective use of medical device products. The State Administration of Pharmaceuticals decides that the nation’s medical devices are producing products. Registration of the status of the registration.