{"id":504,"date":"2026-06-01T10:00:56","date_gmt":"2026-06-01T07:00:56","guid":{"rendered":"http:\/\/sw-themes.com\/porto_dummy\/?post_type=faq&#038;p=504"},"modified":"2026-06-02T13:53:17","modified_gmt":"2026-06-02T10:53:17","slug":"is-iso-13485-certification-mandatory-for-medical-devices","status":"publish","type":"faq","link":"https:\/\/demo.erayonetim.com\/en\/sss\/tibbi-cihaz-iso-13485-belgesi-zorunlu-mudur\/","title":{"rendered":"Is ISO 13485 certification mandatory for medical devices?"},"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>For medical device manufacturers, this document is a fundamental corporate requirement for complying with legal regulations (MDRs), primarily CE certification, and for confidently entering global markets.<\/p>\n<p>&nbsp;<\/p>\n\r\n\t\t<\/div>\r\n\t<\/div>\r\n<\/div><\/div><\/div><!-- \/wp:post-content --><\/div>","protected":false},"template":"","faq_cat":[],"class_list":["post-504","faq","type-faq","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq\/504","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=504"}],"wp:term":[{"taxonomy":"faq_cat","embeddable":true,"href":"https:\/\/demo.erayonetim.com\/en\/wp-json\/wp\/v2\/faq_cat?post=504"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}