国家药监局日前发出通知 ,决定就医疗器械的注册情况进行全面的清理规范。据了解 ,这次清理范围是2 0 0 1年 12月 31日前发出、目前仍在有效期内的医疗器械注册证 ,及其相对应的产品情况。高风险产品和社会反映较多、存在争议的产品将作为本次清理工作的重点 ,包括 :骨科内固定 State Food and Drug Administration recently issued a circular to decide on the registration of medical devices to conduct a comprehensive clean-up specification. It is understood that this clearance range is issued before December 31, 2001 and is still valid for registration of medical devices and their corresponding products. High-risk products and social reactions are more, controversial products will be the focus of this clean-up work, including: orthopedic internal fixation