{"id":3041,"date":"2021-11-23T11:31:14","date_gmt":"2021-11-23T03:31:14","guid":{"rendered":"https:\/\/regask.com\/?p=3041"},"modified":"2024-10-25T02:05:32","modified_gmt":"2024-10-24T18:05:32","slug":"reglamento-de-dispositivos-medicos-de-la-eaeu","status":"publish","type":"post","link":"https:\/\/regask.com\/es\/eaeu-medical-device-regulations\/","title":{"rendered":"El Reglamento centralizado sobre productos sanitarios de la UEEA entra en vigor"},"content":{"rendered":"

A partir del 1 de enero de 2022, la Uni\u00f3n Econ\u00f3mica Euroasi\u00e1tica (UEE), formada por Bielorrusia, Kazajst\u00e1n, Rusia, Armenia y Kirguist\u00e1n, aplicar\u00e1 la nueva regulaci\u00f3n com\u00fan para productos sanitarios que su organismo regulador, la Comisi\u00f3n Econ\u00f3mica Euroasi\u00e1tica (CEE), ha estado desarrollando durante los dos \u00faltimos a\u00f1os.<\/p>\n

El nuevo reglamento armoniza los requisitos para los productos sanitarios con los pa\u00edses de la UEE y establece un procedimiento de registro com\u00fan. Este nuevo registro se presentar\u00e1 ante las autoridades competentes de uno de los Estados miembros, que dirigir\u00e1 el proceso, pero ser\u00e1 v\u00e1lido para toda la UEE.<\/p>\n

Los pr\u00f3ximos registros deber\u00e1n presentarse de acuerdo con el nuevo procedimiento a partir del 1 de enero de 2022. Los registros nacionales existentes que expiren despu\u00e9s de esa fecha seguir\u00e1n siendo v\u00e1lidos como m\u00e1ximo hasta el 31 de diciembre de 2026. A partir del 1 de enero de 2027, todos los dispositivos m\u00e9dicos comercializados en la UEEA deber\u00e1n registrarse de acuerdo con el nuevo reglamento.<\/p>\n

Comun\u00edquese con RegASK para obtener m\u00e1s informaci\u00f3n sobre los cambios en la regulaci\u00f3n de dispositivos m\u00e9dicos. Ponte en contacto con los expertos de RegASK.<\/a><\/p>\n

 <\/p>\n\n\t\tContacte con RegASK para m\u00e1s detalles<\/span>\n\t<\/a>\n\n\n\t\tLeer m\u00e1s<\/span>\n\t<\/a>\n\n

\n\n\t
\n\t\t\t\t
\n\t\t\t\n\t\t\t\n\n\t\tLea estudios de casos de la industria de dispositivos m\u00e9dicos<\/span>\n\t<\/a>\n\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\n\t\n<\/div>","protected":false},"excerpt":{"rendered":"

A partir del 1 de enero de 2022, la Uni\u00f3n Econ\u00f3mica Euroasi\u00e1tica (UEE), formada por Bielorrusia, Kazajist\u00e1n, Rusia, Armenia y Kirguist\u00e1n, aplicar\u00e1 el nuevo reglamento com\u00fan para productos sanitarios que su organismo regulador, la Comisi\u00f3n Econ\u00f3mica Euroasi\u00e1tica (CEE), ha estado desarrollando durante los \u00faltimos dos a\u00f1os. El nuevo reglamento armoniza los requisitos de los productos sanitarios junto con\u2026<\/p>","protected":false},"author":39,"featured_media":3003,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[522,39],"tags":[40],"class_list":["post-3041","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-russia-regulations","category-medical-devices-insights","tag-latest-insights"],"acf":[],"yoast_head":"\nEAEU Medical Device Regulations | RegASK<\/title>\n<meta name=\"description\" content=\"New centralized medical device regulations are in force in the EAEU. 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Ensure compliance with RegASK's guidance.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/regask.com\/es\/reglamento-de-dispositivos-medicos-de-la-eaeu\/\" \/>\n<meta property=\"og:site_name\" content=\"RegASK\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/RegASKRegulatoryAffairs\/\" \/>\n<meta property=\"article:published_time\" content=\"2021-11-23T03:31:14+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-10-24T18:05:32+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/regask.com\/wp-content\/uploads\/2021\/10\/brain-nervous-system-medical-device.png\" \/>\n\t<meta property=\"og:image:width\" content=\"689\" \/>\n\t<meta property=\"og:image:height\" content=\"626\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Benoit Trouwaert\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@ASKRegASK\" \/>\n<meta name=\"twitter:site\" content=\"@ASKRegASK\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Benoit Trouwaert\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutos\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/\"},\"author\":{\"name\":\"Benoit Trouwaert\",\"@id\":\"https:\\\/\\\/regask.com\\\/#\\\/schema\\\/person\\\/c1d261e8dcf7b1c30b2c4f2c119df42d\"},\"headline\":\"EAEU Centralised Medical Devices Regulation Enters in F…\",\"datePublished\":\"2021-11-23T03:31:14+00:00\",\"dateModified\":\"2024-10-24T18:05:32+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/\"},\"wordCount\":237,\"publisher\":{\"@id\":\"https:\\\/\\\/regask.com\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/regask.com\\\/wp-content\\\/uploads\\\/2021\\\/10\\\/brain-nervous-system-medical-device.png\",\"keywords\":[\"Latest Insights\"],\"articleSection\":[\"Russia\",\"Medical Devices\"],\"inLanguage\":\"es\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/\",\"url\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/\",\"name\":\"EAEU Medical Device Regulations | RegASK\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/regask.com\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/regask.com\\\/eaeu-medical-device-regulations\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/regask.com\\\/wp-content\\\/uploads\\\/2021\\\/10\\\/brain-nervous-system-medical-device.png\",\"datePublished\":\"2021-11-23T03:31:14+00:00\",\"dateModified\":\"2024-10-24T18:05:32+00:00\",\"description\":\"New centralized medical device regulations are in force in the EAEU. 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