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From 26 May 2022, all Class A non-sterile devices (such as laboratory instruments), regardless of whether new or already on the market; CE-marked devices that do not need any involvement of notified bodies under the IVDR;

Charleen okeeffeDepartment of healthAuthority of irelandEuropean commissionNational standardsVitro diagnostic medical devices directiveMedical devicesKey milestonesOfficial journalStandards listIvdr crunch time x2013 where does ireland standLife sciencesLife sciencesIotechnology amp nanotechnology