医疗器械标签和说明书管理规定-医疗事故法律援助-法律咨询免费平台-国际律师联盟

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问题	医疗器械标签和说明书管理规定
释义	法律分析： 1、医疗器械标签是指在医疗器械或者包装上附有的，用于识别产品特征的文字说明及图形、符号。 2、医疗器械说明书应当符合国家标准或者行业标准有关要求。法律依据：《医疗器械说明书、标签和包装标识管理规定》第二条凡在中华人民共和国境内销售、使用的医疗器械应当按照本规定要求附有说明书、标签和包装标识。简单易用的产品，按照国家食品药品监督管理局的规定，可以省略说明书、标签和包装标识3项中的某1项或者某2项的，依照其规定。
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