China has a new medical device classification catalog: what you need to know
Grace Fu Palma, China Med Device
The China Food and Drug Administration (CFDA) recently unveiled its new “Medical Device Classification Catalogue” – which has significant implications for medical devices registrations or renewals.
The new catalog, announced Aug. 31 after a previous draft release and feedback period, goes into effect in less than a year – on Aug. 1, 2018.
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Source: Mass Device - Category: Medical Devices Authors: MassDevice Tags: Regulatory/Compliance China Food & Drug Administration (CFDA) Source Type: news