{"id":225115,"date":"2026-02-19T17:01:41","date_gmt":"2026-02-19T14:01:41","guid":{"rendered":"https:\/\/new-inbit.dev-praxis.gr\/?post_type=hta_library&#038;p=225115"},"modified":"2026-02-19T17:01:41","modified_gmt":"2026-02-19T14:01:41","slug":"commission-communication-in-the-framework-of-the-implementation-of-the-council-directive-93-42-eec-concerning-medical-devices","status":"publish","type":"hta_library","link":"https:\/\/www.inbit.gr\/el\/hta_library\/commission-communication-in-the-framework-of-the-implementation-of-the-council-directive-93-42-eec-concerning-medical-devices\/","title":{"rendered":"Commission communication in the framework of the implementation of the Council Directive 93\/ 42\/EEC concerning medical devices"},"content":{"rendered":"\n<p>\u00a0Publication of titles and references of harmonised standards under Union harmonisation legislation<\/p>\n","protected":false},"featured_media":0,"template":"","categories":[19],"tags":[],"class_list":["post-225115","hta_library","type-hta_library","status-publish","hentry","category-other"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/hta_library\/225115","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=225115"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/categories?post=225115"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.inbit.gr\/el\/wp-json\/wp\/v2\/tags?post=225115"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}