{"id":8123,"date":"2025-10-10T10:56:12","date_gmt":"2025-10-10T10:56:12","guid":{"rendered":"https:\/\/kmslaser.com\/?p=8123"},"modified":"2025-10-16T02:18:29","modified_gmt":"2025-10-16T02:18:29","slug":"las-maquinas-de-terapia-de-ondas-de-choque-importadas-necesitan-pruebas-y-certificacion-de-laboratorio-independientes","status":"publish","type":"post","link":"https:\/\/kmslaser.com\/es\/do-imported-shockwave-therapy-machines-need-independent-lab-testing-and-certification\/","title":{"rendered":"\u00bfLas m\u00e1quinas importadas de terapia de ondas de choque necesitan pruebas y certificaci\u00f3n de laboratorio independientes?"},"content":{"rendered":"<p><iframe data-testid=\"embed-iframe\" style=\"border-radius:12px\" src=\"https:\/\/open.spotify.com\/embed\/episode\/3bfi1MjQjtHIq8wnqfsOZK?utm_source=generator&amp;theme=0\" width=\"100%\" height=\"152\" frameborder=\"0\" allowfullscreen=\"\" allow=\"autoplay; clipboard-write; encrypted-media; fullscreen; picture-in-picture\" loading=\"lazy\"><\/iframe><\/p>\n<p style=\"float: right; margin-left: 15px; margin-bottom: 15px;\">\n  <img decoding=\"async\" src=\"https:\/\/kmslaser.com\/wp-content\/uploads\/2025\/10\/1show-a-sterile-laboratory-bay-with-an-accredited-t.jpg\" alt=\"Ingeniero probando equipo m\u00e9dico en entorno de laboratorio (ID#1)\" class=\"top-image-square\">\n<\/p>\n<p>Vendo m\u00e1quinas de belleza y terapia en el extranjero cada mes, y he aprendido una verdad simple: sin certificaci\u00f3n independiente, el despacho de aduanas puede detenerlo todo.<\/p>\n<p><strong>S\u00ed, las m\u00e1quinas importadas de terapia de ondas de choque requieren pruebas y certificaci\u00f3n independientes antes de ingresar a la mayor\u00eda de los mercados regulados. Los laboratorios acreditados verifican la seguridad, el rendimiento y la calidad, garantizando el cumplimiento de las normas de la FDA, CE u otras normas nacionales de dispositivos m\u00e9dicos.<\/strong><\/p>\n<p>Las pruebas no son solo papeleo. Protege a los pacientes, mejora la aceptaci\u00f3n de la cl\u00ednica y previene retrasos en la aduana. Las siguientes secciones explican qu\u00e9 laboratorios son reconocidos a nivel mundial, qu\u00e9 certificaciones se requieren, si las pruebas afectan el tiempo de env\u00edo y c\u00f3mo se comparten los informes con los compradores.<\/p>\n<hr \/>\n<h2>\u00bfQu\u00e9 laboratorios son reconocidos en todo el mundo?<\/h2>\n<p>Como proveedor, siempre animo a los clientes a confiar en los certificados de laboratorios globales acreditados. Estas organizaciones son de confianza para los reguladores y facilitan la verificaci\u00f3n de la documentaci\u00f3n de cumplimiento.<\/p>\n<p><strong>Los laboratorios reconocidos a nivel mundial incluyen T\u00dcV S\u00dcD, T\u00dcV Rheinland, UL Solutions, Intertek, SGS, Eurofins, DEKRA, CSA Group, Nemko y Bureau Veritas. Todos est\u00e1n <a href=\"https:\/\/ilac.org\/accreditation\/iso-iec-17025\/\">acreditados por ISO\/IEC 17025<\/a> <sup><a href=\"#footnote-1\" id=\"ref-1\">1<\/a><\/sup> y autorizados para pruebas de conformidad de dispositivos m\u00e9dicos.<\/strong><\/p>\n<p><img decoding=\"async\" src=\"https:\/\/kmslaser.com\/wp-content\/uploads\/2025\/10\/2t-v-s-d-t-v-rheinland-ul-solutions-intertek-sg.jpg\" alt=\"Certificaciones de organizaciones de pruebas internacionales mostradas en la pared (ID#2)\" title=\"Certificaciones globales\" \/><\/p>\n<p>Cada regi\u00f3n se basa en designaciones ligeramente diferentes. La <strong>UE<\/strong> utiliza <a href=\"https:\/\/webgate.ec.europa.eu\/nando\/\">Organismos Notificados listados en NANDO<\/a> <sup><a href=\"#footnote-2\" id=\"ref-2\">2<\/a><\/sup> para el Marcado CE bajo MDR. El <strong>EE. UU.<\/strong> reconoce <a href=\"https:\/\/www.osha.gov\/nationally-recognized-testing-laboratory-program\">Laboratorios de Pruebas Reconocidos Nacionalmente (NRTL)<\/a> <sup><a href=\"#footnote-3\" id=\"ref-3\">3<\/a><\/sup> como UL o Intertek. El <a href=\"https:\/\/www.iecee.org\/\">Esquema CB IECEE<\/a> <sup><a href=\"#footnote-4\" id=\"ref-4\">4<\/a><\/sup> permite la transferencia de resultados de pruebas entre pa\u00edses. El <strong>Reino Unido<\/strong> utiliza <a href=\"https:\/\/www.gov.uk\/guidance\/using-the-ukca-marking\">Organismos Aprobados para UKCA<\/a> <sup><a href=\"#footnote-5\" id=\"ref-5\">5<\/a><\/sup>, mientras que <strong>Canad\u00e1<\/strong> se basa en laboratorios reconocidos por SCC como CSA Group.<\/p>\n<table>\n<thead>\n<tr>\n<th>Tipo de Laboratorio \/ Organismo<\/th>\n<th>Ejemplos<\/th>\n<th>Rol Principal<\/th>\n<th>Mercado Clave<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Laboratorios de Pruebas ISO\/IEC 17025<\/td>\n<td>T\u00dcV S\u00dcD, SGS, Eurofins<\/td>\n<td>Realizar pruebas de seguridad y EMC<\/td>\n<td>Global<\/td>\n<\/tr>\n<tr>\n<td>Certificaci\u00f3n \/ Organismos Notificados<\/td>\n<td>DEKRA, BSI, T\u00dcV Rheinland<\/td>\n<td>Revisar archivos t\u00e9cnicos, emitir CE\/UKCA<\/td>\n<td>UE \/ Reino Unido<\/td>\n<\/tr>\n<tr>\n<td>NRTL (EE. UU.)<\/td>\n<td>UL, ETL (Intertek), CSA<\/td>\n<td>Certificar la seguridad del producto<\/td>\n<td>Estados Unidos<\/td>\n<\/tr>\n<tr>\n<td>Esquema CB IECEE<\/td>\n<td>Red mundial<\/td>\n<td>Armonizar aprobaciones multipa\u00eds<\/td>\n<td>Importaciones globales<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>Consejos de verificaci\u00f3n:<\/strong><\/p>\n<ul>\n<li>Compruebe si la acreditaci\u00f3n del laboratorio incluye <strong>IEC 60601<\/strong> and <strong>ISO 10993<\/strong> normas.<\/li>\n<li>Confirme la inclusi\u00f3n del laboratorio en las bases de datos de <strong>IECEE<\/strong>, <strong>FDA ASCA<\/strong>, o <strong>EU NANDO<\/strong> databases.<\/li>\n<li>Solicite el <strong>certificado de alcance de acreditaci\u00f3n<\/strong> del laboratorio e incl\u00fayalo en el expediente t\u00e9cnico.<\/li>\n<\/ul>\n<hr \/>\n<h2>\u00bfQu\u00e9 certificaciones se requieren habitualmente?<\/h2>\n<p>Explico a los compradores que cada mercado define la seguridad y el rendimiento de manera diferente, pero la mayor\u00eda comparte la misma base internacional.<\/p>\n<p><strong>Las certificaciones comunes incluyen IEC 60601-1 para seguridad el\u00e9ctrica, IEC 60601-1-2 para compatibilidad electromagn\u00e9tica, ISO 10993 para biocompatibilidad, ISO 13485 para gesti\u00f3n de calidad y aprobaciones CE\/FDA\/UKCA\/CSA seg\u00fan el destino.<\/strong><\/p>\n<p><img decoding=\"async\" src=\"https:\/\/kmslaser.com\/wp-content\/uploads\/2025\/10\/3depict-a-quality-manager-reviewing-an-iso-13485-ce.jpg\" alt=\"Gerente de control de calidad auditando informes de cumplimiento en una computadora port\u00e1til (ID#3)\" title=\"Revisi\u00f3n de auditor\u00eda de calidad\" \/><\/p>\n<p>Las m\u00e1quinas de terapia de ondas de choque se consideran equipos el\u00e9ctricos m\u00e9dicos. Deben pasar la verificaci\u00f3n de dise\u00f1o y las pruebas independientes de seguridad el\u00e9ctrica, seguridad mec\u00e1nica y estabilidad de rendimiento. Las piezas de mano o accesorios que entran en contacto con la piel deben cumplir las normas de biocompatibilidad. El fabricante tambi\u00e9n debe implementar un sistema de gesti\u00f3n de calidad certificado seg\u00fan la norma ISO 13485.<\/p>\n<table>\n<thead>\n<tr>\n<th>Capa de Certificaci\u00f3n<\/th>\n<th>Requisito T\u00edpico<\/th>\n<th>Qu\u00e9 cubre<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Seguridad El\u00e9ctrica<\/td>\n<td>IEC 60601-1<\/td>\n<td>Corriente de fuga, aislamiento, puesta a tierra<\/td>\n<\/tr>\n<tr>\n<td>EMC<\/td>\n<td>IEC 60601-1-2<\/td>\n<td>Emisi\u00f3n e inmunidad contra interferencias<\/td>\n<\/tr>\n<tr>\n<td>Biocompatibilidad<\/td>\n<td>ISO 10993<\/td>\n<td>Compatibilidad con piel, mucosas y tejidos<\/td>\n<\/tr>\n<tr>\n<td>Gesti\u00f3n de Riesgos<\/td>\n<td>ISO 14971<\/td>\n<td>An\u00e1lisis de peligros y controles de riesgos<\/td>\n<\/tr>\n<tr>\n<td>Sistema de Calidad<\/td>\n<td>ISO 13485<\/td>\n<td>Procedimientos de producci\u00f3n y trazabilidad<\/td>\n<\/tr>\n<tr>\n<td>Aprobaci\u00f3n de Mercado<\/td>\n<td>CE, FDA, UKCA, CSA<\/td>\n<td>Venta legal en la regi\u00f3n objetivo<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Los fabricantes tambi\u00e9n pueden necesitar probar par\u00e1metros adicionales, como <strong>salida ac\u00fastica<\/strong>, <strong>durabilidad del aplicador<\/strong>, y <strong>calibraci\u00f3n de energ\u00eda<\/strong>. Los accesorios que contengan materiales met\u00e1licos, pl\u00e1sticos o de gel deben incluir evaluaciones de seguridad qu\u00edmica y biol\u00f3gica. Para la mayor\u00eda de los requisitos el\u00e9ctricos y de EMC, consulte este resumen de <a href=\"https:\/\/www.intertek.com\/medical\/iec-60601-testing\/\">pruebas de dispositivos m\u00e9dicos IEC 60601<\/a> <sup><a href=\"#footnote-6\" id=\"ref-6\">6<\/a><\/sup>, y para materiales, consulte <a href=\"https:\/\/www.fda.gov\/medical-devices\/biocompatibility-assessment-medical-devices\">gu\u00eda de biocompatibilidad ISO 10993<\/a> <sup><a href=\"#footnote-7\" id=\"ref-7\">7<\/a><\/sup>. Los sistemas de calidad se demuestran a trav\u00e9s de <a href=\"https:\/\/www.iso.org\/standard\/59752.html\">certificaci\u00f3n ISO 13485<\/a> <sup><a href=\"#footnote-8\" id=\"ref-8\">8<\/a><\/sup> y gesti\u00f3n de riesgos seg\u00fan <a href=\"https:\/\/www.iso.org\/standard\/72704.html\">ISO 14971<\/a> <sup><a href=\"#footnote-9\" id=\"ref-9\">9<\/a><\/sup>. Para el cumplimiento de la CE seg\u00fan MDR, consulte la <a href=\"https:\/\/health.ec.europa.eu\/medical-devices-sector\/new-regulations_en\">gu\u00eda de marcado CE para dispositivos m\u00e9dicos de la UE<\/a> <sup><a href=\"#footnote-10\" id=\"ref-10\">10<\/a><\/sup>.<\/p>\n<hr \/>\n<h2>\u00bfLas pruebas independientes retrasan el env\u00edo?<\/h2>\n<p>Siempre advierto a los clientes que las pruebas no planificadas pueden detener un env\u00edo durante semanas. La programaci\u00f3n temprana evita esto.<\/p>\n<p><strong>Las pruebas independientes pueden retrasar el env\u00edo si comienzan despu\u00e9s de la producci\u00f3n, pero la planificaci\u00f3n de las pruebas durante el desarrollo del producto mantiene la entrega a tiempo. Los programas de prueba completos suelen tardar de 4 a 10 semanas, dependiendo de la carga de trabajo del laboratorio y la complejidad del dispositivo.<\/strong><\/p>\n<p><img decoding=\"async\" src=\"https:\/\/kmslaser.com\/wp-content\/uploads\/2025\/10\/4show-a-scheduling-war-room-view-a-gantt-chart-wit.jpg\" alt=\"Equipo revisando el cronograma de pruebas de laboratorio y certificaci\u00f3n (ID#4)\" title=\"Planificaci\u00f3n del proceso de certificaci\u00f3n\" \/><\/p>\n<p>El tiempo de prueba depende de cuatro cosas: la programaci\u00f3n del laboratorio, la preparaci\u00f3n de la muestra, las necesidades de repetici\u00f3n de pruebas y la revisi\u00f3n de documentos. Una prueba completa de IEC 60601 puede llevar seis semanas, mientras que las pruebas de EMC o biocompatibilidad pueden agregar varias m\u00e1s. Si un proveedor ya tiene informes v\u00e1lidos, este tiempo desaparece.<\/p>\n<table>\n<thead>\n<tr>\n<th>Paso del proceso<\/th>\n<th>Duraci\u00f3n t\u00edpica<\/th>\n<th>C\u00f3mo evitar retrasos<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Definir el alcance de la prueba<\/td>\n<td>1\u20132 semanas<\/td>\n<td>Bloquear la lista est\u00e1ndar temprano<\/td>\n<\/tr>\n<tr>\n<td>Reserva de laboratorio<\/td>\n<td>1\u20133 semanas<\/td>\n<td>Reservar espacio durante el ensamblaje<\/td>\n<\/tr>\n<tr>\n<td>Pruebas<\/td>\n<td>2\u20136 semanas<\/td>\n<td>Proporcionar dos muestras<\/td>\n<\/tr>\n<tr>\n<td>Acciones correctivas<\/td>\n<td>1\u20133 semanas<\/td>\n<td>Mantener ingenieros en espera<\/td>\n<\/tr>\n<tr>\n<td>Informar problema<\/td>\n<td>1\u20132 semanas<\/td>\n<td>Enviar documentos temprano<\/td>\n<\/tr>\n<tr>\n<td>Revisi\u00f3n del organismo de certificaci\u00f3n<\/td>\n<td>2\u20138 semanas<\/td>\n<td>Responder r\u00e1pidamente a los comentarios<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>Mejor pr\u00e1ctica:<\/strong> solicitar <em>modelos precertificados<\/em> con documentaci\u00f3n IEC 60601 o CE existente. Esto permite el env\u00edo inmediato sin repetir ciclos completos de laboratorio.<\/p>\n<hr \/>\n<h2>\u00bfSe comparten los informes de pruebas con los compradores?<\/h2>\n<p>Cuando exporto dispositivos, incluyo un paquete de cumplimiento en cada env\u00edo; los compradores nunca deber\u00edan tener que adivinar qu\u00e9 normas se probaron.<\/p>\n<p><strong>S\u00ed, los proveedores comparten informes de prueba independientes o res\u00famenes de certificaci\u00f3n con los compradores. Los informes completos pueden compartirse bajo un acuerdo de confidencialidad, mientras que los documentos de cumplimiento p\u00fablico (certificado CE, DoC, certificado ISO) siempre se incluyen.<\/strong><\/p>\n<p><img decoding=\"async\" src=\"https:\/\/kmslaser.com\/wp-content\/uploads\/2025\/10\/5illustrate-a-discreet-nda-signing-between-buyer-an.jpg\" alt=\"Acuerdo de confidencialidad y documentos en la mesa de reuni\u00f3n corporativa (ID#5)\" title=\"Configuraci\u00f3n de acuerdo de confidencialidad\" \/><\/p>\n<p>La mayor\u00eda de los proveedores proporcionan una <strong>carpeta de cumplimiento<\/strong> que contiene:<\/p>\n<ul>\n<li>Certificados de aprobaci\u00f3n CE o FDA<\/li>\n<li>Declaraci\u00f3n de Conformidad (DoC)<\/li>\n<li>Documentos ISO 13485 e ISO 14971<\/li>\n<li>Res\u00famenes de seguridad y EMC IEC 60601<\/li>\n<li>Datos de calibraci\u00f3n y rendimiento<\/li>\n<\/ul>\n<p>Si el comprador necesita el informe t\u00e9cnico completo (para licitaciones o presentaciones regulatorias), el proveedor puede liberarlo bajo un acuerdo de confidencialidad. Esto mantiene los secretos comerciales protegidos mientras satisface las necesidades de documentaci\u00f3n oficial.<\/p>\n<table>\n<thead>\n<tr>\n<th>Tipo de Documento<\/th>\n<th>Objetivo<\/th>\n<th>Pol\u00edtica de Compartilhamento<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td>Certificados CE \/ FDA \/ UKCA<\/td>\n<td>Autoriza\u00e7\u00e3o de Mercado<\/td>\n<td>Sempre compartilhado<\/td>\n<\/tr>\n<tr>\n<td>Certificado ISO 13485<\/td>\n<td>Comprovante de gest\u00e3o de qualidade<\/td>\n<td>Sempre compartilhado<\/td>\n<\/tr>\n<tr>\n<td>Resumo do teste IEC 60601-1<\/td>\n<td>Seguran\u00e7a el\u00e9trica<\/td>\n<td>Resumo compartilhado, completo sob NDA<\/td>\n<\/tr>\n<tr>\n<td>Relat\u00f3rio de teste de EMC<\/td>\n<td>Emiss\u00e3o e imunidade<\/td>\n<td>Compartilhado mediante solicita\u00e7\u00e3o<\/td>\n<\/tr>\n<tr>\n<td>Relat\u00f3rio de biocompatibilidade<\/td>\n<td>Seguran\u00e7a do material<\/td>\n<td>Compartilhado mediante solicita\u00e7\u00e3o<\/td>\n<\/tr>\n<tr>\n<td>Resumo de gest\u00e3o de riscos<\/td>\n<td>Conformidade do projeto<\/td>\n<td>Compartido bajo NDA<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<hr \/>\n<h2>Consejos pr\u00e1cticos de cumplimiento para importadores<\/h2>\n<p>Antes de realizar un pedido, solicite una <strong>lista de verificaci\u00f3n de cumplimiento<\/strong> al proveedor. Debe enumerar todos los mercados de destino, est\u00e1ndares y nombres de laboratorios. Solicite <strong>certificados de muestra<\/strong> o informes de prueba, y aseg\u00farese de que el nombre del modelo en el informe coincida con su producto. Esto evita detenciones aduaneras y re-pruebas de importaci\u00f3n.<\/p>\n<p>Cuando lleguen las m\u00e1quinas, realice una breve <strong>verificaci\u00f3n de aceptaci\u00f3n en el sitio<\/strong>\u2014prueba de puesta a tierra, verificaci\u00f3n de salida y coincidencia del n\u00famero de serie\u2014para confirmar que el env\u00edo se alinea con su documentaci\u00f3n de prueba.<\/p>\n<hr \/>\n<h2>Conclusi\u00f3n<\/h2>\n<p>Las pruebas y certificaciones de laboratorio independientes son obligatorias para la importaci\u00f3n segura y legal de m\u00e1quinas de terapia de ondas de choque. Elija laboratorios acreditados, verifique la lista de est\u00e1ndares antes de la producci\u00f3n y recopile todos los documentos de cumplimiento antes del env\u00edo para mantener las aduanas fluidas y las operaciones sin preocupaciones.<\/p>\n<hr \/>\n<h2>Notas al pie<\/h2>\n<p><span id=\"footnote-1\">1. Resumen de ILAC de la acreditaci\u00f3n ISO\/IEC 17025 para laboratorios de pruebas. <a href=\"#ref-1\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-2\">2. Base de datos NANDO de la UE que enumera los Organismos Notificados para el marcado CE. <a href=\"#ref-2\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-3\">3. Programa de OSHA que describe el reconocimiento NRTL en los EE. UU. <a href=\"#ref-3\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-4\">4. Esquema CB de IECEE: reconocimiento mutuo de informes de prueba de productos. <a href=\"#ref-4\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-5\">5. Gu\u00eda del Reino Unido sobre el marcado UKCA y los Organismos Aprobados. <a href=\"#ref-5\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-6\">6. Gu\u00eda de Intertek sobre pruebas de seguridad\/EMC IEC 60601. <a href=\"#ref-6\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-7\">7. Recurso de la FDA sobre la evaluaci\u00f3n de biocompatibilidad ISO 10993. <a href=\"#ref-7\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-8\">8. P\u00e1gina del est\u00e1ndar ISO 13485 para SGC de dispositivos m\u00e9dicos. <a href=\"#ref-8\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-9\">9. Resumen del est\u00e1ndar de gesti\u00f3n de riesgos ISO 14971. <a href=\"#ref-9\">\u21a9\ufe0e<\/a><\/span><br \/>\n<span id=\"footnote-10\">10. Orientaci\u00f3n de la UE MDR\/marcado CE para dispositivos m\u00e9dicos. <a href=\"#ref-10\">\u21a9\ufe0e<\/a><\/span>  <\/p>","protected":false},"excerpt":{"rendered":"<p>I sell beauty and therapy machines overseas every month, and I\u2019ve learned one simple truth: without independent certification, customs clearance can stop everything. Yes, imported shockwave therapy machines require independent testing and certification before entering most regulated markets. Accredited laboratories verify safety, performance, and quality, ensuring compliance with FDA, CE, or other national medical-device standards. [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":8129,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"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":"default","adv-header-id-meta":"","stick-header-meta":"default","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[1],"tags":[],"class_list":["post-8123","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v27.0 (Yoast SEO v28.1) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Do imported Shockwave Therapy Machines need independent lab testing and certification? - KMSLaser<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/kmslaser.com\/es\/las-maquinas-de-terapia-de-ondas-de-choque-importadas-necesitan-pruebas-y-certificacion-de-laboratorio-independientes\/\" \/>\n<meta property=\"og:locale\" content=\"es_MX\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Do imported Shockwave Therapy Machines need independent lab testing and certification?\" \/>\n<meta property=\"og:description\" content=\"I sell beauty and therapy machines overseas every month, and I\u2019ve learned one simple truth: without independent certification, customs clearance can stop everything. 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