{"id":7988,"date":"2022-12-22T15:40:28","date_gmt":"2022-12-22T14:40:28","guid":{"rendered":"https:\/\/www.accessafe.eu\/technical-file\/"},"modified":"2026-07-17T15:43:23","modified_gmt":"2026-07-17T13:43:23","slug":"ficha-tecnica","status":"publish","type":"post","link":"https:\/\/www.accessafe.eu\/es\/ficha-tecnica\/","title":{"rendered":"Ficha t\u00e9cnica"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">El expediente t\u00e9cnico es el conjunto de<strong> documentos que <\/strong>demuestran que<strong> la <\/strong>m\u00e1quina<strong> cumple <\/strong>con <strong>los requisitos esenciales de seguridad<\/strong> (R.E.S. <strong>).<\/strong><\/p>\n\n<p class=\"wp-block-paragraph\">Este documento permite a las autoridades encargadas de la vigilancia del mercado comprobar f\u00e1cilmente que la m\u00e1quina en cuesti\u00f3n cumple con la normativa.<\/p>\n\n<p class=\"wp-block-paragraph\">La responsabilidad de elaborar el expediente t\u00e9cnico recae en <strong>el fabricante<\/strong> <strong>de la m\u00e1quina<\/strong>.<br\/>Si la m\u00e1quina se importa de un <strong>pa\u00eds fuera de la UE<\/strong>, donde el fabricante no est\u00e1 obligado a elaborarlo, esta responsabilidad recae<strong>en el importador<\/strong> o en <strong>el representante autorizado.<\/strong><\/p>\n\n<p class=\"wp-block-paragraph\">Tiene que estar redactado obligatoriamente en <strong>una<\/strong> o <strong>varias lenguas de la Uni\u00f3n Europea<\/strong> y debe estar a <strong>disposici\u00f3n de las autoridades<\/strong> competentes de los Estados miembros durante al menos 10 a\u00f1os a partir de su publicaci\u00f3n o redacci\u00f3n.<\/p>\n\n<h2 class=\"wp-block-heading\">LOS DOCUMENTOS DEL EXPEDIENTE T\u00c9CNICO<\/h2>\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n<p class=\"wp-block-paragraph\">Tal y como se define en el anexo VII de la Directiva sobre m\u00e1quinas 2006\/42\/CE, el <strong>expediente t\u00e9cnico est\u00e1 <\/strong>compuesto por los siguientes documentos:<\/p>\n\n<ul class=\"wp-block-list\">\n<li><strong>Descripci\u00f3n general<\/strong> de la m\u00e1quina<\/li>\n\n\n\n<li><strong>el dise\u00f1o general<\/strong> de la m\u00e1quina, <strong>los esquemas<\/strong> de los circuitos de control, as\u00ed como las descripciones y explicaciones necesarias para entender c\u00f3mo <strong>funciona<\/strong> la m\u00e1quina<\/li>\n\n\n\n<li><strong>planos detallados<\/strong> y completos, que pueden ir acompa\u00f1ados de notas de c\u00e1lculo, resultados de ensayos y certificados; esta informaci\u00f3n debe permitir comprobar que la m\u00e1quina cumple los requisitos esenciales de seguridad y protecci\u00f3n de la salud,<\/li>\n\n\n\n<li>documentaci\u00f3n relativa a <strong>la evaluaci\u00f3n de riesgos<\/strong> que debe demostrar el procedimiento seguido, incluyendo:<\/li>\n<\/ul>\n\n<ol class=\"wp-block-list\">\n<li>lista de <strong>los requisitos<\/strong> esenciales de seguridad y protecci\u00f3n de la salud aplicables a la m\u00e1quina<\/li>\n\n\n\n<li><strong>medidas de protecci\u00f3n<\/strong> aplicadas para eliminar los peligros identificados o para reducir los riesgos; si es necesario, tambi\u00e9n la indicaci\u00f3n de los riesgos residuales relacionados con la m\u00e1quina<\/li>\n<\/ol>\n\n<ul class=\"wp-block-list\">\n<li><strong>las normas<\/strong> y otras <strong>especificaciones t\u00e9cnicas<\/strong> aplicadas que indiquen los requisitos esenciales de seguridad y protecci\u00f3n de la salud que cubren dichas normas,<\/li>\n\n\n\n<li>cualquier <strong>informe t\u00e9cnico<\/strong> que recoja los resultados de los ensayos realizados por el propio fabricante o por un organismo elegido por \u00e9l o por su representante autorizado,<\/li>\n\n\n\n<li>un ejemplar del <strong>manual de instrucciones<\/strong> de la m\u00e1quina,<\/li>\n\n\n\n<li>si procede, de <strong>la declaraci\u00f3n de incorporaci\u00f3n<\/strong> de las cuasi-m\u00e1quinas incluidas y de las correspondientes instrucciones de montaje,<\/li>\n\n\n\n<li>si procede, una copia de <strong>la declaraci\u00f3n CE<\/strong> de conformidad de las m\u00e1quinas o de otros <strong>productos incorporados<\/strong> a la m\u00e1quina,<\/li>\n\n\n\n<li>una copia de <strong>la declaraci\u00f3n CE de conformidad<\/strong>.<\/li>\n<\/ul>\n\n<h3 class=\"has-text-align-left wp-block-heading\">Accessafe \u00e8 parte attiva del gruppo di lavoro \u201cSicurezza del macchinario\u00a0UNI US0010100 e ISO TC 199\u2033<\/h3>\n","protected":false},"excerpt":{"rendered":"<p>El expediente t\u00e9cnico es el conjunto de documentos que demuestran que la m\u00e1quina cumple con los requisitos esenciales de seguridad (R.E.S.).<\/p>\n","protected":false},"author":2,"featured_media":6785,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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