{"id":4661,"date":"2026-07-08T10:03:22","date_gmt":"2026-07-08T07:03:22","guid":{"rendered":"https:\/\/demo.erayonetim.com\/?post_type=faq&#038;p=4661"},"modified":"2026-07-08T10:03:22","modified_gmt":"2026-07-08T07:03:22","slug":"what-is-mdr-2017-745-eu","status":"publish","type":"faq","link":"https:\/\/erayonetim.com\/en\/sss\/mdr-2017-745-eu-nedir\/","title":{"rendered":"What is MDR (2017\/745\/EU)?"},"content":{"rendered":"<div class=\"wpb-content-wrapper\"><div class=\"vc_row wpb_row row top-row wpb_custom_034b39d9bc6c6b310d69e39f0ccf274f\"><div class=\"vc_column_container col-md-12\"><div class=\"wpb_wrapper vc_column-inner\">\r\n\t<div class=\"wpb_text_column wpb_content_element wpb_custom_7c91d232724f73626cc933bd95b25ff0\" >\r\n\t\t<div class=\"wpb_wrapper\">\r\n\t\t\t<p style=\"font-weight: 400;\">MDR (Medical Device Regulation) 2017\/745 is the European Union&#039;s current legislation on medical devices. The MDR introduces more comprehensive requirements than previous directives regarding product safety, clinical evidence, traceability, and post-marketing surveillance.<\/p>\n\r\n\t\t<\/div>\r\n\t<\/div>\r\n<\/div><\/div><\/div>\n<\/div>","protected":false},"template":"","faq_cat":[],"class_list":["post-4661","faq","type-faq","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/erayonetim.com\/en\/wp-json\/wp\/v2\/faq\/4661","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/erayonetim.com\/en\/wp-json\/wp\/v2\/faq"}],"about":[{"href":"https:\/\/erayonetim.com\/en\/wp-json\/wp\/v2\/types\/faq"}],"wp:attachment":[{"href":"https:\/\/erayonetim.com\/en\/wp-json\/wp\/v2\/media?parent=4661"}],"wp:term":[{"taxonomy":"faq_cat","embeddable":true,"href":"https:\/\/erayonetim.com\/en\/wp-json\/wp\/v2\/faq_cat?post=4661"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}