{"id":6565,"date":"2026-05-25T11:09:35","date_gmt":"2026-05-25T05:39:35","guid":{"rendered":"https:\/\/operonstrategist.com\/?p=6565"},"modified":"2026-05-25T11:11:23","modified_gmt":"2026-05-25T05:41:23","slug":"understanding-legacy-medical-devices","status":"publish","type":"post","link":"https:\/\/operonstrategist.com\/br-en\/understanding-legacy-medical-devices\/","title":{"rendered":"Legacy Medical Devices &#8211; Manufacturers Need to Know about Legacy Devices"},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-post\" data-elementor-id=\"6565\" class=\"elementor elementor-6565\" data-elementor-post-type=\"post\">\n\t\t\t\t<div class=\"elementor-element elementor-element-c9fcd0a e-flex e-con-boxed e-con e-parent\" data-id=\"c9fcd0a\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t<div class=\"elementor-element elementor-element-640ed27c e-con-full e-flex e-con e-child\" data-id=\"640ed27c\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-3f196af1 elementor-widget elementor-widget-heading\" data-id=\"3f196af1\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Legacy Medical Devices &#8211; Manufacturers Need to Know about Legacy Devices<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-71b22f71 elementor-widget elementor-widget-text-editor\" data-id=\"71b22f71\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">In May 2021, the European Union Commission implemented medical device regulation (MDR) 2017\/745 to make medical devices safer, more effective, and easy to trace. As per the new MDR, a manufacturer must comply with the CE certificate to sell medical devices in the European market. <\/span><\/p><p><span style=\"font-weight: 400;\">As a <\/span><a href=\"https:\/\/operonstrategist.com\/services\/regulatory-approvals\/ce-marking\/\"><span style=\"font-weight: 400;\">CE-marked medical device consultant<\/span><\/a><span style=\"font-weight: 400;\">, we assist and guide manufacturers in ensuring their devices\u2019 regulatory compliance. A few devices were placed per the medical device directive 90\/385\/EEC or 93\/42\/EEC.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-43b64ccf e-con-full e-flex e-con e-child\" data-id=\"43b64ccf\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t<div class=\"elementor-element elementor-element-58e1c5b6 e-con-full e-flex e-con e-child\" data-id=\"58e1c5b6\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t<div class=\"elementor-element elementor-element-3f2d7698 elementor-widget elementor-widget-heading\" data-id=\"3f2d7698\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h4 class=\"elementor-heading-title elementor-size-default\">Talk to our experts<\/h4>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-3ff3b300 elementor-widget elementor-widget-wpforms\" data-id=\"3ff3b300\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"wpforms.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t<div class=\"wpforms-container wpforms-container-full wpforms-render-modern\" id=\"wpforms-6203\"><form id=\"wpforms-form-6203\" class=\"wpforms-validate wpforms-form wpforms-ajax-form\" data-formid=\"6203\" method=\"post\" enctype=\"multipart\/form-data\" action=\"\/br-en\/wp-json\/wp\/v2\/posts\/6565\" data-token=\"a9cf6cd8d4000495d77213cf2045c3d0\" data-token-time=\"1780630398\"><noscript class=\"wpforms-error-noscript\">Please enable JavaScript in your browser to complete this form.<\/noscript><div id=\"wpforms-error-noscript\" style=\"display: none;\">Please enable JavaScript in your browser to complete this form.<\/div><div class=\"wpforms-field-container\"><div id=\"wpforms-6203-field_1-container\" class=\"wpforms-field wpforms-field-name\" data-field-id=\"1\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_1\" aria-hidden=\"false\">Name <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><input type=\"text\" id=\"wpforms-6203-field_1\" class=\"wpforms-field-large wpforms-field-required\" name=\"wpforms[fields][1]\" placeholder=\"Name*\" aria-errormessage=\"wpforms-6203-field_1-error\" required><\/div>\t\t<div id=\"wpforms-6203-field_5-container\"\n\t\t\tclass=\"wpforms-field wpforms-field-text\"\n\t\t\tdata-field-type=\"text\"\n\t\t\tdata-field-id=\"5\"\n\t\t\t>\n\t\t\t<label class=\"wpforms-field-label\" for=\"wpforms-6203-field_5\" >Name Text Email<\/label>\n\t\t\t<input type=\"text\" id=\"wpforms-6203-field_5\" class=\"wpforms-field-medium\" name=\"wpforms[fields][5]\" >\n\t\t<\/div>\n\t\t<div id=\"wpforms-6203-field_2-container\" class=\"wpforms-field wpforms-field-email\" data-field-id=\"2\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_2\" aria-hidden=\"false\">Email <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><input type=\"email\" id=\"wpforms-6203-field_2\" class=\"wpforms-field-large wpforms-field-required\" name=\"wpforms[fields][2]\" placeholder=\"Email*\" spellcheck=\"false\" aria-errormessage=\"wpforms-6203-field_2-error\" required><\/div><div id=\"wpforms-6203-field_3-container\" class=\"wpforms-field wpforms-field-phone\" data-field-id=\"3\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_3\" aria-hidden=\"false\">Phone <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><input type=\"tel\" id=\"wpforms-6203-field_3\" class=\"wpforms-field-large wpforms-field-required wpforms-smart-phone-field\" data-rule-smart-phone-field=\"true\" name=\"wpforms[fields][3]\" placeholder=\"Phone*\" aria-label=\"Phone\" aria-errormessage=\"wpforms-6203-field_3-error\" required><\/div><div id=\"wpforms-6203-field_4-container\" class=\"wpforms-field wpforms-field-textarea\" data-field-id=\"4\"><label class=\"wpforms-field-label wpforms-label-hide\" for=\"wpforms-6203-field_4\" aria-hidden=\"false\">Paragraph Text <span class=\"wpforms-required-label\" aria-hidden=\"true\">*<\/span><\/label><textarea id=\"wpforms-6203-field_4\" class=\"wpforms-field-medium wpforms-field-required\" name=\"wpforms[fields][4]\" placeholder=\"Message\" aria-errormessage=\"wpforms-6203-field_4-error\" required><\/textarea><\/div><script>\n\t\t\t\t( function() {\n\t\t\t\t\tconst style = document.createElement( 'style' );\n\t\t\t\t\tstyle.appendChild( document.createTextNode( '#wpforms-6203-field_5-container { position: absolute !important; overflow: hidden !important; display: inline !important; height: 1px !important; width: 1px !important; z-index: -1000 !important; padding: 0 !important; } #wpforms-6203-field_5-container input { visibility: hidden; } #wpforms-conversational-form-page #wpforms-6203-field_5-container label { counter-increment: none; }' ) );\n\t\t\t\t\tdocument.head.appendChild( style );\n\t\t\t\t\tdocument.currentScript?.remove();\n\t\t\t\t} )();\n\t\t\t<\/script><\/div><!-- .wpforms-field-container --><div class=\"wpforms-recaptcha-container wpforms-is-recaptcha wpforms-is-recaptcha-type-v3\" ><input type=\"hidden\" name=\"wpforms[recaptcha]\" value=\"\"><\/div><div class=\"wpforms-submit-container\" ><input type=\"hidden\" name=\"wpforms[id]\" value=\"6203\"><input type=\"hidden\" name=\"page_title\" value=\"\"><input type=\"hidden\" name=\"page_url\" value=\"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/posts\/6565\"><input type=\"hidden\" name=\"url_referer\" value=\"\"><button type=\"submit\" name=\"wpforms[submit]\" id=\"wpforms-submit-6203\" class=\"wpforms-submit\" data-alt-text=\"Sending...\" data-submit-text=\"Submit\" aria-live=\"assertive\" value=\"wpforms-submit\">Submit<\/button><img decoding=\"async\" src=\"https:\/\/operonstrategist.com\/wp-content\/plugins\/wpforms\/assets\/images\/submit-spin.svg\" class=\"wpforms-submit-spinner\" style=\"display: none;\" width=\"26\" height=\"26\" alt=\"Loading\"><\/div><\/form><\/div>  <!-- .wpforms-container -->\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t<div class=\"elementor-element elementor-element-5b16dcee e-flex e-con-boxed e-con e-parent\" data-id=\"5b16dcee\" data-element_type=\"container\" data-e-type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-14be7bd elementor-widget elementor-widget-text-editor\" data-id=\"14be7bd\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">The manufacturers of those devices are confused about how they can continue to sell their medical devices. <\/span><span style=\"font-weight: 400;\">To overcome this confusion European Commission came up with a new guidance called Medical Device Coordination Group (MDGC) 2021-25, which explains the requirements of legacy medical devices and all those devices which were placed on the market before the implementation of medical device regulations in 2017\/745 along with addressing the issues of putting legacy medical devices in the European market.\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-6407dcf elementor-widget elementor-widget-heading\" data-id=\"6407dcf\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">What is a Legacy Medical device? \n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-17ab5206 elementor-widget elementor-widget-text-editor\" data-id=\"17ab5206\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Legacy medical devices are defined or understood as those placed on the market after the implementation of medical device regulations 2017\/745 as per article 120(3) of the MDR. They will be in the market until 26 May 2024 if they fulfill certain conditions. Those devices are:\u00a0<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Class I medical devices were under the medical device directive 93\/42\/EEC, for which EC, also called CE, was drawn before 26 May 2021, and for CE procedure under the MDR, a notified body is involved.\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">A device with a valid EC certificate issued as per Directive 90\/385\/EEC (AIMDD) or the MDD before 26 May 2021.\u00a0<\/span><\/li><\/ul><p><i><span style=\"font-weight: 400;\">MDGC 2021-25 tells the difference between an old device and a legacy medical device:<\/span><\/i><span style=\"font-weight: 400;\">\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">Old device: All those devices were placed on the market before the implementation of medical device regulations 2017\/745 and complied with AIMDD or the MDD. They followed the applicable rules before these directives came into effect.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">MDR devices are those devices that are placed in the market as per the MDR 2017\/745.\u00a0<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-64eac2a elementor-widget elementor-widget-heading\" data-id=\"64eac2a\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">MDR requirements applicable to legacy medical devices: \n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-15bb2dc elementor-widget elementor-widget-text-editor\" data-id=\"15bb2dc\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Manufacturers and importers can place the medical device which complies with the MDR (Article 10(1) and 13 (1) MDR). In contrast, legacy medical devices must comply with the medical device directive (MDD) or AIMDD and d few additional requirements present in article 120(3) of the MDR. Additionally, economic operators (manufacturers, importers, distributors, and authorized representatives) too have to follow a few provisions for their legacy medical devices:\u00a0<\/span><\/p><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">for manufacturers they can follow Article 10 (10), (12)-(15);\u00a0\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">for authorized representatives they can follow Article 11(3)(c)-(g);\u00a0\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">for importers they can follow Article 13(2), 2nd subparagraph, (4), (6)-(8), (10);\u00a0<\/span><\/li><\/ul><ul><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">for distributors they can follow Article 14(2), last subparagraph, (4)-(6).\u00a0<\/span><\/li><li style=\"font-weight: 400;\" aria-level=\"1\"><span style=\"font-weight: 400;\">Based on this approach, the relevant working groups may identify further requirements applicable to \u2018legacy devices.<\/span><\/li><\/ul><p>\u00a0<\/p><table><tbody><tr><td><p><span style=\"font-weight: 400;\">MDR requirements\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">Applicability to Legacy medical devices\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 10(10), (12)-(15)\u00a0\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES conformity with the requirements of this Regulation shall mean for \u2018legacy devices\u2019 conformity with the MDD or AIMDD and the additional requirements per Article 120(3) MDR)\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 11(3)(c)-(g)\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES conformity with the requirements of this Regulation shall mean for \u2018legacy devices\u2019 conformity with the MDD or AIMDD and the additional requirements per Article 120(3) MDR)\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 11(7)\u00a0\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 13(2)\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\"> 2nd subparagraph, (4), (6)-(8), (10) YES conformity with the requirements of this Regulation shall mean for \u2018legacy devices\u2019 conformity with the MDD or AIMDD and the additional requirements per Article 120(3) MDR)\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 14(2) \u2013 last subparagraph, (4)-(6)\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES conformity with the requirements of this Regulation shall mean for \u2018legacy devices\u2019 conformity with the MDD or AIMDD and the additional requirements per Article 120(3) MDR)\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 29- registration of devices\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">In principle, YES, but in the absence of EUDAMED\u2019s full functionality, specific transitional provisions apply per Art. 122, 123(3)(d)(e) MDR10\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 31 \u2013 registration of economic operators\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">In principle, YES, but in the absence of EUDAMED\u2019s full functionality, specific transitional provisions apply per Art. 122, 123(3)(d)(e) MDR1\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 83, 84 \u2013 PMS system and PMS plan\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES (with exception of requirements that relate to non-applicable obligations, e.g. Art. 83(3)(d) \u2013 SSCP; no requirement for a full revision of the technical documentation per Annexes II and III)\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 85 \u2013 PMS report (class I devices)\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">PMS report (class I devices) YES (classification of devices in class I follows classification rules of the MDD, i.e. Art. 85 applies to class I \u2018legacy devices\u2019 even though those devices might be in a higher class under the MDR)\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 86 \u2013 PSUR (class IIa, IIb, and III devices)\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES (manufacturers shall draw up and update PSURs; to be taken into consideration by a notified body designated under AIMDD\/MDD in the framework of surveillance audits.\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 87 \u2013serious incident reporting\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES\u00a0\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 88 \u2013 trend reporting\u00a0\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES (trend reporting was already part of the vigilance system established under the MDD\/AIMDD)\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 89 \u2013serious incidents analysis and FSCA\u00a0\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 90 \u2013vigilance data analysis\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">analysis of vigilance data YES\u00a0\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 91 \u2013 implementing acts\u00a0\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">YES\u00a0<\/span><\/p><\/td><\/tr><tr><td><p><span style=\"font-weight: 400;\">Art. 92 \u2013 EUDAMED vigilance module\u00a0<\/span><\/p><\/td><td><p><span style=\"font-weight: 400;\">In principle, YES, but in the absence of EUDAMED\u2019s full functionality, specific transitional provisions apply per Art. 122, 123(3)(d)(e) MDR\u00a0<\/span><\/p><\/td><\/tr><\/tbody><\/table><p>\u00a0<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-b3ecfb8 elementor-widget elementor-widget-heading\" data-id=\"b3ecfb8\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"heading.default\">\n\t\t\t\t\t<h2 class=\"elementor-heading-title elementor-size-default\">Relaxation to legacy medical devices: \n<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<div class=\"elementor-element elementor-element-9ab049f elementor-widget elementor-widget-text-editor\" data-id=\"9ab049f\" data-element_type=\"widget\" data-e-type=\"widget\" data-widget_type=\"text-editor.default\">\n\t\t\t\t\t\t\t\t\t<p><span style=\"font-weight: 400;\">Up to 2024, the transitional period of MDR, there is some relaxation to the medical devices. The legacy medical devices can remain in the market after the implementation of MDR, i.e. May 2021, if certain conditions are met and can be put in service as well.<\/span><\/p><p><span style=\"font-weight: 400;\">With every amendment, a medical device becomes a legacy medical device, and the European Union commission is well aware of this fact. That\u2019s why there is always a transitional period along with some MDGC guidance that helps the manufacturer continue selling their devices in the market. Manufacturers must pay close attention to the amendment and how it will affect their devices. Then only they will be able to use the transitional period and understand and work according to the guidance. As <\/span><a href=\"https:\/\/operonstrategist.com\/\"><span style=\"font-weight: 400;\">medical device regulatory consultant,<\/span><\/a><span style=\"font-weight: 400;\"> we provide guidance at every step of manufacturing the devices as per the required regulations.<\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>In May 2021, the European Union Commission implemented medical device regulation (MDR) 2017\/745 to make medical devices safer, more effective, and easy to trace. As per the new MDR, a manufacturer must comply with the CE certificate to sell medical devices in the European market. As a CE-marked medical device consultant, we assist and guide [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":6599,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[16],"tags":[],"class_list":["post-6565","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medical-device-manufacturing"],"_links":{"self":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/posts\/6565","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/comments?post=6565"}],"version-history":[{"count":0,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/posts\/6565\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/media\/6599"}],"wp:attachment":[{"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/media?parent=6565"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/categories?post=6565"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/operonstrategist.com\/br-en\/wp-json\/wp\/v2\/tags?post=6565"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}