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CFDA issues Provisions for Medical Device Recall
2017-02-09

The newly revised Regulations for the Supervision and Administration of Medical Devices has been implemented from June 1, 2014, which presents new requirements to the recall of medical devices. China Food and Drug Administration (CFDA) organized the revision of the Provisions for Medical Device Recall (interim), and formulated the Provisions for Medical Device Recall. The Provisions for Medical Device Recall (CFDA Order No. 29) was adopted at the executive meeting of China Food and Drug Administration on January 5, 2017, and shall be effective as of May 1, 2017.

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