{"id":45405,"date":"2021-02-22T15:36:46","date_gmt":"2021-02-22T20:36:46","guid":{"rendered":"https:\/\/regstaging.wpengine.com\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/"},"modified":"2021-02-23T12:31:48","modified_gmt":"2021-02-23T17:31:48","slug":"fda-cancels-31-of-medical-device-registrations-for-failure-to-renew","status":"publish","type":"post","link":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/","title":{"rendered":"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o"},"content":{"rendered":"<p>Em fevereiro de 2021, a Administra\u00e7\u00e3o de Alimentos e Medicamentos (FDA) dos Estados Unidos removeu 13.455 estabelecimentos de dispositivos m\u00e9dicos e suas listagens de dispositivos associados de seu banco de dados de registro. Isso resultou em uma diminui\u00e7\u00e3o de 31% no n\u00famero total de estabelecimentos de dispositivos m\u00e9dicos registrados pela FDA.<\/p>\n<p>Os estabelecimentos de dispositivos m\u00e9dicos devem renovar anualmente seus registros no FDA entre 1\u00ba de outubro e 31 de dezembro. O FDA considera os registros que n\u00e3o s\u00e3o renovados antes do prazo como &#8220;expirados&#8221; e, logo ap\u00f3s cada per\u00edodo de renova\u00e7\u00e3o, remove as instala\u00e7\u00f5es que n\u00e3o foram renovadas de seu banco de dados.<\/p>\n<p>Em 22 de fevereiro de 2021, havia 29.678 estabelecimentos de dispositivos registrados no banco de dados da FDA em compara\u00e7\u00e3o com 43.133 registrados em dezembro de 2020. Os pa\u00edses com mais registros exclu\u00eddos foram China, Estados Unidos, Coreia do Sul, Vietn\u00e3 e Turquia.<\/p>\n<p><strong>Como posso saber se meu registro foi exclu\u00eddo?<\/strong><\/p>\n<p>O FDA normalmente n\u00e3o notifica os estabelecimentos quando eles s\u00e3o removidos de seus registros. Muitos estabelecimentos n\u00e3o percebem que seus registros expiraram at\u00e9 que suas remessas sejam interrompidas pelos funcion\u00e1rios de conformidade da FDA no porto de entrada nos Estados Unidos.<\/p>\n<p>Registrar Corp pode ajudar a verificar sem nenhum custo se seu registro foi renovado com sucesso para o per\u00edodo de 2021. <a href=\"https:\/\/regstaging.wpengine.com\/fda-medical-devices\/registration\/verification\/?lead_source=blog\">Clique aqui para verificar seu registro<\/a>.<\/p>\n<p><strong>O que devo fazer se meu registro foi exclu\u00eddo?<\/strong><\/p>\n<p>A distribui\u00e7\u00e3o de dispositivos m\u00e9dicos vencidos nos Estados Unidos \u00e9 proibida e pode sujeitar o propriet\u00e1rio do estabelecimento a penalidades civis ou criminais. Os estabelecimentos com registros expirados devem se registrar novamente no FDA, obter um novo n\u00famero de registro e registrar novamente seus dispositivos antes de continuar a comercializar seus dispositivos m\u00e9dicos nos Estados Unidos.<\/p>\n<p>Mais de 30.000 empresas em todo o mundo confiam na Registrar Corp para gerenciar seus registros do FDA. Registrar Corp pode <a href=\"https:\/\/regstaging.wpengine.com\/fda-medical-devices\/registration\/?lead_source=blog\">registrar novamente seu estabelecimento<\/a> com sucesso. Como parte de nosso servi\u00e7o de registro, as empresas recebem suporte regulamentar ao longo do ano, incluindo monitoramento de suas instala\u00e7\u00f5es para conformidade com o FDA, assist\u00eancia para deten\u00e7\u00e3o e muito mais. Para obter mais informa\u00e7\u00f5es, entre em contato com Registrar Corp em + 1-757-224-0177 ou converse com um consultor regulat\u00f3rio 24 horas por dia no seguinte link: regstaging.wpengine.com\/livechat.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Em fevereiro de 2021, a Administra\u00e7\u00e3o de Alimentos e Medicamentos (FDA) dos Estados Unidos removeu 13.455 estabelecimentos de dispositivos m\u00e9dicos e suas listagens de dispositivos associados de seu banco de dados de registro. Isso resultou em uma diminui\u00e7\u00e3o de 31% no n\u00famero total de estabelecimentos de dispositivos m\u00e9dicos registrados pela FDA. Os estabelecimentos de dispositivos<\/p>\n","protected":false},"author":2,"featured_media":39535,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"content-type":"","om_disable_all_campaigns":false,"inline_featured_image":false,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","footnotes":""},"categories":[44],"tags":[],"class_list":{"0":"post-45405","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-uncategorized-pt","8":"entry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v20.9 (Yoast SEO v25.5) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o - Registrar<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"pt_PT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o\" \/>\n<meta property=\"og:description\" content=\"Em fevereiro de 2021, a Administra\u00e7\u00e3o de Alimentos e Medicamentos (FDA) dos Estados Unidos removeu 13.455 estabelecimentos de dispositivos m\u00e9dicos e suas listagens de dispositivos associados de seu banco de dados de registro. Isso resultou em uma diminui\u00e7\u00e3o de 31% no n\u00famero total de estabelecimentos de dispositivos m\u00e9dicos registrados pela FDA. Os estabelecimentos de dispositivos\" \/>\n<meta property=\"og:url\" content=\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/\" \/>\n<meta property=\"og:site_name\" content=\"Registrar\" \/>\n<meta property=\"article:published_time\" content=\"2021-02-22T20:36:46+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2021-02-23T17:31:48+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1650\" \/>\n\t<meta property=\"og:image:height\" content=\"500\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"admin\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"admin\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/\"},\"author\":{\"name\":\"admin\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/person\/9562a5d4aefe254f6c4fd9b51d9f7cb6\"},\"headline\":\"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o\",\"datePublished\":\"2021-02-22T20:36:46+00:00\",\"dateModified\":\"2021-02-23T17:31:48+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/\"},\"wordCount\":412,\"publisher\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#organization\"},\"image\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg\",\"articleSection\":[\"Uncategorized @pt\"],\"inLanguage\":\"pt\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/\",\"url\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/\",\"name\":\"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o - Registrar\",\"isPartOf\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage\"},\"image\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg\",\"datePublished\":\"2021-02-22T20:36:46+00:00\",\"dateModified\":\"2021-02-23T17:31:48+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#breadcrumb\"},\"inLanguage\":\"pt\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"pt\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage\",\"url\":\"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg\",\"contentUrl\":\"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg\",\"width\":1650,\"height\":500},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https:\/\/legacy.registrarcorp.com\/pt\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#website\",\"url\":\"https:\/\/legacy.registrarcorp.com\/pt\/\",\"name\":\"Registrar\",\"description\":\"Assistance with U.S. FDA Regulations\",\"publisher\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/legacy.registrarcorp.com\/pt\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"pt\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#organization\",\"name\":\"Registrar Corp\",\"url\":\"https:\/\/legacy.registrarcorp.com\/pt\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"pt\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/logo\/image\/\",\"url\":\"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/12\/regcorp_logo.png\",\"contentUrl\":\"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/12\/regcorp_logo.png\",\"width\":1326,\"height\":330,\"caption\":\"Registrar Corp\"},\"image\":{\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/logo\/image\/\"}},{\"@type\":\"Person\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/person\/9562a5d4aefe254f6c4fd9b51d9f7cb6\",\"name\":\"admin\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"pt\",\"@id\":\"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/secure.gravatar.com\/avatar\/d26b6ba384aad0d13f9acfd54cae897432d061de92870ea21ff5125e381ae564?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/secure.gravatar.com\/avatar\/d26b6ba384aad0d13f9acfd54cae897432d061de92870ea21ff5125e381ae564?s=96&d=mm&r=g\",\"caption\":\"admin\"},\"sameAs\":[\"https:\/\/regstaging.wpengine.com\"],\"url\":\"https:\/\/legacy.registrarcorp.com\/pt\/author\/registrar\/\"}]}<\/script>\n<!-- \/ Yoast SEO Premium plugin. -->","yoast_head_json":{"title":"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o - Registrar","robots":{"index":"noindex","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"og_locale":"pt_PT","og_type":"article","og_title":"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o","og_description":"Em fevereiro de 2021, a Administra\u00e7\u00e3o de Alimentos e Medicamentos (FDA) dos Estados Unidos removeu 13.455 estabelecimentos de dispositivos m\u00e9dicos e suas listagens de dispositivos associados de seu banco de dados de registro. Isso resultou em uma diminui\u00e7\u00e3o de 31% no n\u00famero total de estabelecimentos de dispositivos m\u00e9dicos registrados pela FDA. Os estabelecimentos de dispositivos","og_url":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/","og_site_name":"Registrar","article_published_time":"2021-02-22T20:36:46+00:00","article_modified_time":"2021-02-23T17:31:48+00:00","og_image":[{"width":1650,"height":500,"url":"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg","type":"image\/jpeg"}],"author":"admin","twitter_card":"summary_large_image","twitter_misc":{"Written by":"admin","Est. reading time":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#article","isPartOf":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/"},"author":{"name":"admin","@id":"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/person\/9562a5d4aefe254f6c4fd9b51d9f7cb6"},"headline":"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o","datePublished":"2021-02-22T20:36:46+00:00","dateModified":"2021-02-23T17:31:48+00:00","mainEntityOfPage":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/"},"wordCount":412,"publisher":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/#organization"},"image":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage"},"thumbnailUrl":"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg","articleSection":["Uncategorized @pt"],"inLanguage":"pt"},{"@type":"WebPage","@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/","url":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/","name":"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o - Registrar","isPartOf":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/#website"},"primaryImageOfPage":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage"},"image":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage"},"thumbnailUrl":"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg","datePublished":"2021-02-22T20:36:46+00:00","dateModified":"2021-02-23T17:31:48+00:00","breadcrumb":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#breadcrumb"},"inLanguage":"pt","potentialAction":[{"@type":"ReadAction","target":["https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/"]}]},{"@type":"ImageObject","inLanguage":"pt","@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#primaryimage","url":"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg","contentUrl":"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/08\/press_release.jpg","width":1650,"height":500},{"@type":"BreadcrumbList","@id":"https:\/\/legacy.registrarcorp.com\/pt\/fda-cancels-31-of-medical-device-registrations-for-failure-to-renew\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Home","item":"https:\/\/legacy.registrarcorp.com\/pt\/"},{"@type":"ListItem","position":2,"name":"O FDA cancelou 31% dos registros de dispositivos m\u00e9dicos por falta de renova\u00e7\u00e3o"}]},{"@type":"WebSite","@id":"https:\/\/legacy.registrarcorp.com\/pt\/#website","url":"https:\/\/legacy.registrarcorp.com\/pt\/","name":"Registrar","description":"Assistance with U.S. FDA Regulations","publisher":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/legacy.registrarcorp.com\/pt\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"pt"},{"@type":"Organization","@id":"https:\/\/legacy.registrarcorp.com\/pt\/#organization","name":"Registrar Corp","url":"https:\/\/legacy.registrarcorp.com\/pt\/","logo":{"@type":"ImageObject","inLanguage":"pt","@id":"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/logo\/image\/","url":"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/12\/regcorp_logo.png","contentUrl":"https:\/\/legacy.registrarcorp.com\/wp-content\/uploads\/2019\/12\/regcorp_logo.png","width":1326,"height":330,"caption":"Registrar Corp"},"image":{"@id":"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/logo\/image\/"}},{"@type":"Person","@id":"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/person\/9562a5d4aefe254f6c4fd9b51d9f7cb6","name":"admin","image":{"@type":"ImageObject","inLanguage":"pt","@id":"https:\/\/legacy.registrarcorp.com\/pt\/#\/schema\/person\/image\/","url":"https:\/\/secure.gravatar.com\/avatar\/d26b6ba384aad0d13f9acfd54cae897432d061de92870ea21ff5125e381ae564?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/d26b6ba384aad0d13f9acfd54cae897432d061de92870ea21ff5125e381ae564?s=96&d=mm&r=g","caption":"admin"},"sameAs":["https:\/\/regstaging.wpengine.com"],"url":"https:\/\/legacy.registrarcorp.com\/pt\/author\/registrar\/"}]}},"_links":{"self":[{"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/posts\/45405","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/comments?post=45405"}],"version-history":[{"count":0,"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/posts\/45405\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/media\/39535"}],"wp:attachment":[{"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/media?parent=45405"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/categories?post=45405"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/legacy.registrarcorp.com\/pt\/wp-json\/wp\/v2\/tags?post=45405"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}