EU: Common Specifications for the reprocessing of single-use devices
EU: EUDAMED actor registration module to launch in December 2020
EU: Guidance on adverse incident reporting of insulin infusion pumps and integrated meter systems
EU: Notified Bodies may use MDSAP reports to inform their surveillance activities
Ireland: Proposed medical device fees for 2021
Ireland: Basic check list issued to help Class I manufacturers comply with the MDR
Netherlands: Emergency use of non-CE-marked medical devices has now ended
Portugal: New Medical Device Information System (SIDM) to be launched
Switzerland: Information leaflet updated on exemptions for non-compliant devices
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