{"id":14318,"date":"2020-04-30T15:55:22","date_gmt":"2020-04-30T13:55:22","guid":{"rendered":"https:\/\/www.red-on-line-ehs.co.uk\/ehs\/?p=6082"},"modified":"2022-07-07T05:26:39","modified_gmt":"2022-07-07T03:26:39","slug":"ireland-covid-19-authorise-non-ce-marked-medical-devices","status":"publish","type":"post","link":"https:\/\/www.red-on-line.com\/gb\/blog\/ireland-covid-19-authorise-non-ce-marked-medical-devices\/","title":{"rendered":"Ireland | COVID-19 | The Minister for Health is given the power to authorise non-CE marked medical devices"},"content":{"rendered":"In the context of the Covid-19 emergency, the Minister for Health is given the\u00a0power to authorise the placing on the market or putting into service of non-CE marked medical devices. Consequently, the European Communities (Medical Devices) Regulations 1994 and the European Communities (In Vitro Diagnostic Medical Devices) Regulations 2001 are amended.\n\nSource:\n\nS.I. No. 144 of 2020. EUROPEAN COMMUNITIES (MEDICAL DEVICES) (AMENDMENT) REGULATIONS 20<\/a>20\n\nS.I. No. 145 of 2020. EUROPEAN COMMUNITIES (IN VITRO DIAGNOSTIC MEDICAL DEVICES) (AMENDMENT) REGULATIONS 2020.","protected":false},"excerpt":{"rendered":"

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