{"id":12324,"date":"2019-08-29T14:36:16","date_gmt":"2019-08-29T12:36:16","guid":{"rendered":"https:\/\/eudamed.eu\/?page_id=12324"},"modified":"2026-04-14T19:43:01","modified_gmt":"2026-04-14T17:43:01","slug":"eudamed-ivdr-and-mdr-ec-regulations","status":"publish","type":"page","link":"https:\/\/eudamed.com\/index.php\/eudamed-ivdr-and-mdr-ec-regulations\/","title":{"rendered":"IVDR and MDR Regulations"},"content":{"rendered":"<p>[vc_row css=&#8221;.vc_custom_1463600795244{margin-bottom: 0px !important;padding-top: 80px !important;padding-bottom: 110px !important;}&#8221;][vc_column][vc_row_inner gap=&#8221;30&#8243; css=&#8221;.vc_custom_1463592469581{padding-right: 15px !important;padding-bottom: 60px !important;padding-left: 15px !important;}&#8221;][vc_column_inner offset=&#8221;vc_col-md-offset-2 vc_col-md-8&#8243;][vc_column_text css_animation=&#8221;bottom-to-top&#8221; css=&#8221;.vc_custom_1532952679558{margin-bottom: 12px !important;}&#8221;]<\/p>\n<h6 style=\"color: #693a67; text-align: center;\">We are the MDR Eudamed specialists<\/h6>\n<p>[\/vc_column_text][vc_column_text css_animation=&#8221;bottom-to-top&#8221;]<\/p>\n<h1 style=\"text-align: center;\">EUDAMED, IVDR, and MDR<\/h1>\n<h2 style=\"text-align: center;\">European Commission Regulations<\/h2>\n<p>[\/vc_column_text][vc_column_text css_animation=&#8221;bottom-to-top&#8221; css=&#8221;.vc_custom_1567086092825{margin-bottom: 60px !important;}&#8221;]<\/p>\n<p style=\"text-align: left;\">\n<table id=\"tablepress-1\" class=\"tablepress tablepress-id-1\">\n<thead>\n<tr class=\"row-1\">\n\t<th class=\"column-1\">Publication<\/th><th class=\"column-2\">Searchable HTML<\/th><th class=\"column-3\">PDF<\/th>\n<\/tr>\n<\/thead>\n<tbody class=\"row-striping row-hover\">\n<tr class=\"row-2\">\n\t<td class=\"column-1\">Medical Device Regulation MDR  (EU) 2017\/745 Consolidated<\/td><td class=\"column-2\"><a href=\"https:\/\/eudamed.eu\/index.php\/european-medical-device-regulation-consolidated-mdr-eudamed\/\" rel=\"noopener noreferrer\" target=\"_blank\">European Medical Device Regulation (MDR) EUDAMED Consolidated<\/a><\/td><td class=\"column-3\"><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/PDF\/?uri=CELEX:02017R0745-20200424&amp;from=EN\" rel=\"noopener noreferrer\" target=\"_blank\">Link<\/a><\/td>\n<\/tr>\n<tr class=\"row-3\">\n\t<td class=\"column-1\">Medical Device Regulation MDR  (EU) 2017\/745<\/td><td class=\"column-2\"><a href=\"https:\/\/eudamed.eu\/index.php\/european-medical-device-regulation-mdr-eudamed\/\" rel=\"noopener noreferrer\" target=\"_blank\">European Medical Device Regulation (MDR) EUDAMED<\/a><\/td><td class=\"column-3\"><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/?uri=CELEX:02017R0745-20170505\" rel=\"noopener noreferrer\" target=\"_blank\">Link<\/a><\/td>\n<\/tr>\n<tr class=\"row-4\">\n\t<td class=\"column-1\">Medical Device Regulation MDR  (EU) 2017\/745 Corrigendum<\/td><td class=\"column-2\"><a href=\"https:\/\/eudamed.eu\/index.php\/european-medical-device-regulation-mdr-corrigendum-eudamed\/\" rel=\"noopener noreferrer\" target=\"_blank\">European Medical Device Regulation (MDR) Corrigendum EUDAMED<\/a><\/td><td class=\"column-3\"><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/PDF\/?uri=CELEX:32017R0745R(01)&amp;qid=1556876003672&amp;from=EN\" rel=\"noopener noreferrer\" target=\"_blank\">Link<\/a><\/td>\n<\/tr>\n<tr class=\"row-5\">\n\t<td class=\"column-1\">Medical Device Regulation MDR  (EU) 2017\/745 Corrigendum II<\/td><td class=\"column-2\"><a href=\"https:\/\/eudamed.eu\/index.php\/european-medical-device-regulation-mdr-corrigendum-2-eudamed\/\" rel=\"noopener noreferrer\" target=\"_blank\">European Medical Device Regulation (MDR) Corrigendum EUDAMED<\/a><\/td><td class=\"column-3\"><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/HTML\/?uri=CELEX:32017R0745R(02)&amp;qid=1580835994365&amp;from=EN\" rel=\"noopener noreferrer\" target=\"_blank\">Link<\/a><\/td>\n<\/tr>\n<tr class=\"row-6\">\n\t<td class=\"column-1\">In Vitro Diagnostic Medical Devices Regulations IVDR (EU) 2017\/746<\/td><td class=\"column-2\"><a href=\"https:\/\/eudamed.eu\/index.php\/european-in-vitro-device-regulation-ivdr-eudamed\/\" rel=\"noopener noreferrer\" target=\"_blank\">European In Vitro Device Regulation  (IVDR) EUDAMED<\/a><\/td><td class=\"column-3\"><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/?uri=CELEX:02017R0746-20170505\" rel=\"noopener noreferrer\" target=\"_blank\">Link<\/a><\/td>\n<\/tr>\n<tr class=\"row-7\">\n\t<td class=\"column-1\">In Vitro Diagnostic Medical Devices Regulations IVDR (EU) 2017\/746 Corrigendum<\/td><td class=\"column-2\"><a href=\"https:\/\/eudamed.eu\/index.php\/european-in-vitro-device-regulation-ivdr-corrigendum-eudamed\/\" rel=\"noopener noreferrer\" target=\"_blank\">European In Vitro Device Regulation (IVDR) Corrigendum EUDAMED<\/a><\/td><td class=\"column-3\"><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/PDF\/?uri=CELEX:32017R0746R(02)&amp;qid=1556876050548&amp;from=EN\" rel=\"noopener noreferrer\" target=\"_blank\">Link<\/a><\/td>\n<\/tr>\n<tr class=\"row-8\">\n\t<td class=\"column-1\">In Vitro Diagnostic Medical Devices Regulations IVDR (EU) 2017\/746 Corrigendum II<\/td><td class=\"column-2\"><a href=\"https:\/\/eudamed.eu\/index.php\/european-in-vitro-device-regulation-ivdr-corrigendum-2-eudamed\/\" rel=\"noopener noreferrer\" target=\"_blank\">European In Vitro Device Regulation (IVDR) Corrigendum EUDAMED<\/a><\/td><td class=\"column-3\"><a href=\"https:\/\/eur-lex.europa.eu\/legal-content\/EN\/TXT\/HTML\/?uri=CELEX:32017R0746R(03)&amp;qid=1580837225819&amp;from=EN\" rel=\"noopener noreferrer\" target=\"_blank\">Link<\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/p>\n<p 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