{"id":500,"date":"2026-06-01T11:00:21","date_gmt":"2026-06-01T08:00:21","guid":{"rendered":"http:\/\/sw-themes.com\/porto_dummy\/?post_type=faq&#038;p=500"},"modified":"2026-06-02T13:54:04","modified_gmt":"2026-06-02T10:54:04","slug":"what-is-mdr-european-medical-device-regulation-and-its-scope","status":"publish","type":"faq","link":"https:\/\/demo.erayonetim.com\/en\/sss\/mdr-avrupa-tibbi-cihaz-regulyasyonu-nedir-kapsami\/","title":{"rendered":"What is the MDR (European Medical Device Regulation) and who does it cover?"},"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>The MDR (European Medical Device Regulation) is a comprehensive set of current legal rules that all medical devices intended for sale on the European Union market must comply with. It directly binds all manufacturers, importers, and distributors in the sector.<\/p>\n<p>&nbsp;<\/p>\n\r\n\t\t<\/div>\r\n\t<\/div>\r\n<\/div><\/div><\/div>\r\n<!-- \/wp:post-content --><\/div>","protected":false},"template":"","faq_cat":[],"class_list":["post-500","faq","type-faq","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq\/500","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq"}],"about":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/types\/faq"}],"wp:attachment":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/media?parent=500"}],"wp:term":[{"taxonomy":"faq_cat","embeddable":true,"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq_cat?post=500"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}