{"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":"2025-08-22T15:20:06","modified_gmt":"2025-08-22T13:20:06","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":"","protected":false},"excerpt":{"rendered":"
In the context of the Covid-19 emergency, the Minister for Health is given the power 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. Source: S.I. No. 144 of 2020. EUROPEAN COMMUNITIES (MEDICAL DEVICES) (AMENDMENT) REGULATIONS 20<\/a>20 S.I. No. 145 of 2020. EUROPEAN COMMUNITIES (IN VITRO DIAGNOSTIC MEDICAL DEVICES) (AMENDMENT) REGULATIONS 2020.<\/p>\n","protected":false},"author":1,"featured_media":5872,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":[],"categories":[591,538],"tags":[],"yoast_head":"\n