{"id":225270,"date":"2026-02-24T11:29:53","date_gmt":"2026-02-24T08:29:53","guid":{"rendered":"https:\/\/new-inbit.dev-praxis.gr\/?post_type=hta_library&#038;p=225270"},"modified":"2026-02-24T11:29:54","modified_gmt":"2026-02-24T08:29:54","slug":"guideline-therapeutic-medical-devices-eunethta","status":"publish","type":"hta_library","link":"https:\/\/www.inbit.gr\/el\/hta_library\/guideline-therapeutic-medical-devices-eunethta\/","title":{"rendered":"Guideline: Therapeutic medical devices | EUnetHTA"},"content":{"rendered":"\n<p>This guideline on \u201cTherapeutic medical devices\u201d, with answered comments from the SAG \/ Public consultation, is the last guideline of WP7 Subgroup 3 in JA2.<\/p>\n","protected":false},"featured_media":0,"template":"","categories":[18],"tags":[],"class_list":["post-225270","hta_library","type-hta_library","status-publish","hentry","category-guidelines"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/hta_library\/225270","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/hta_library"}],"about":[{"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/types\/hta_library"}],"wp:attachment":[{"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/media?parent=225270"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/categories?post=225270"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/tags?post=225270"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}