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Tag Archives: Regulatory Framework for Medical Devices

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borderline and classification medical devices

CE Marking, Minor change, RegulatoryBy NicolasOctober 22, 2014

borderline and classification medical devices: UPDATED MANUAL ON BORDERLINE AND CLASSIFICATION IN THE COMMUNITY REGULATORY FRAMEWORK FOR MEDICAL DEVICES Version 1.16 (07-2014) Borderline cases are considered to be those cases where it is not clear from the outset whether a given product is a medical device, an in vitro diagnostic medical device, an active implantable…

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