{"id":4252,"date":"2025-09-29T11:30:41","date_gmt":"2025-09-29T11:30:41","guid":{"rendered":"https:\/\/cmcmedicaldevices.com\/?p=4252"},"modified":"2025-09-29T11:34:35","modified_gmt":"2025-09-29T11:34:35","slug":"switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices","status":"publish","type":"post","link":"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/","title":{"rendered":"Switzerland adopts EU rules on electronic instructions for use for medical devices"},"content":{"rendered":"<div class=\"fusion-fullwidth fullwidth-box fusion-builder-row-1 fusion-flex-container has-pattern-background has-mask-background nonhundred-percent-fullwidth non-hundred-percent-height-scrolling\" style=\"--awb-border-radius-top-left:0px;--awb-border-radius-top-right:0px;--awb-border-radius-bottom-right:0px;--awb-border-radius-bottom-left:0px;--awb-flex-wrap:wrap;\" ><div class=\"fusion-builder-row fusion-row fusion-flex-align-items-flex-start fusion-flex-content-wrap\" style=\"max-width:1248px;margin-left: calc(-4% \/ 2 );margin-right: calc(-4% \/ 2 );\"><div class=\"fusion-layout-column fusion_builder_column fusion-builder-column-0 fusion_builder_column_1_1 1_1 fusion-flex-column\" style=\"--awb-bg-size:cover;--awb-width-large:100%;--awb-margin-top-large:0px;--awb-spacing-right-large:1.92%;--awb-margin-bottom-large:20px;--awb-spacing-left-large:1.92%;--awb-width-medium:100%;--awb-order-medium:0;--awb-spacing-right-medium:1.92%;--awb-spacing-left-medium:1.92%;--awb-width-small:100%;--awb-order-small:0;--awb-spacing-right-small:1.92%;--awb-spacing-left-small:1.92%;\"><div class=\"fusion-column-wrapper fusion-column-has-shadow fusion-flex-justify-content-flex-start fusion-content-layout-column\"><div class=\"fusion-text fusion-text-1\"><article>\n<header>\n<\/header>\n<p>On 8 August 2025, Swissmedic announced the immediate implementation of <strong><a href=\"https:\/\/eur-lex.europa.eu\/eli\/reg_impl\/2025\/1234\/oj\/eng\" target=\"_blank\" rel=\"noopener noreferrer\">Commission Implementing Regulation (EU)<\/a> 2025\/1234<\/strong> on electronic instructions for use (e-IFUs). The measure aligns Switzerland with the latest EU requirements and extends the permitted scope for e-IFUs when devices are intended for professional users.<\/p>\n<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_74 counter-hierarchy ez-toc-counter ez-toc-grey ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title\" style=\"cursor:inherit\">Table of Contents<\/p>\n<span class=\"ez-toc-title-toggle\"><a href=\"#\" class=\"ez-toc-pull-right ez-toc-btn ez-toc-btn-xs ez-toc-btn-default ez-toc-toggle\" aria-label=\"Alternar tabla de contenidos\"><span class=\"ez-toc-js-icon-con\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewBox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewBox=\"0 0 24 24\" version=\"1.2\" baseProfile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n<nav><ul class='ez-toc-list ez-toc-list-level-1 ' ><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#Overview_of_the_new_EU_provisions\" >Overview of the new EU provisions<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#Repeal_of_the_previous_framework\" >Repeal of the previous framework<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#How_the_change_applies_in_Switzerland\" >How the change applies in Switzerland<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#Impact_on_manufacturers\" >Impact on manufacturers<\/a><ul class='ez-toc-list-level-3' ><li class='ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#1_Broader_use_of_e-IFUs_for_professional_users\" >1. Broader use of e-IFUs for professional users<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#2_Mandatory_registration_of_the_e-IFU_address\" >2. Mandatory registration of the e-IFU address<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#3_Clear_user_segmentation_and_labelling\" >3. Clear user segmentation and labelling<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#4_Operational_and_technical_responsibilities\" >4. Operational and technical responsibilities<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-3'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#5_Harmonised_compliance_across_EU_and_Switzerland\" >5. Harmonised compliance across EU and Switzerland<\/a><\/li><\/ul><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-10\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#What_stakeholders_should_do_next\" >What stakeholders should do next<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-11\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#Conclusion\" >Conclusion<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-12\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/#Reference_and_call_to_action\" >Reference and call to action<\/a><\/li><\/ul><\/nav><\/div>\n<h2 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 40; line-height: 1.2;\" data-fontsize=\"40\" data-lineheight=\"48px\"><span class=\"ez-toc-section\" id=\"Overview_of_the_new_EU_provisions\"><\/span>Overview of the new EU provisions<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>On 25 June 2025, the European Commission adopted <a href=\"https:\/\/eur-lex.europa.eu\/eli\/reg_impl\/2025\/1234\/oj\/eng\" target=\"_blank\" rel=\"noopener noreferrer\">Regulation (EU) 2025\/1234<\/a>, which amends Implementing <a href=\"https:\/\/eur-lex.europa.eu\/eli\/reg_impl\/2021\/2226\/oj\/eng\" target=\"_blank\" rel=\"noopener noreferrer\">Regulation (EU) 2021\/2226<\/a>. The amendment entered into force on 16 July 2025 and broadens the types of devices for which instructions may be provided electronically.<\/p>\n<p>When devices are intended for professional users, the updated rules now permit e-IFUs for:<\/p>\n<ul>\n<li>all medical devices and their accessories;<\/li>\n<li>products without an intended medical purpose listed in Annex XVI to the EU MDR;<\/li>\n<li>legacy devices previously covered under older transitional rules.<\/li>\n<\/ul>\n<p>Instructions for use intended for lay persons must still be supplied in paper form. In addition, manufacturers registering devices must provide <a href=\"https:\/\/health.ec.europa.eu\/medical-devices-eudamed\/udidevice-registration_en\" target=\"_blank\" rel=\"noopener noreferrer\"><b>Eudamed\u2019s UDI <\/b>database<\/a> with the internet address where the e-IFU is hosted.<\/p>\n<h2 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 40; line-height: 1.2;\" data-fontsize=\"40\" data-lineheight=\"48px\"><span class=\"ez-toc-section\" id=\"Repeal_of_the_previous_framework\"><\/span>Repeal of the previous framework<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Regulation (EU) 2025\/1234 repeals Regulation (EU) 207\/2012, which had governed electronic instructions for a subset of legacy devices. With the repeal, the updated implementing regulation now provides a single, broader framework for e-IFUs under the MDR.<\/p>\n<h2 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 40; line-height: 1.2;\" data-fontsize=\"40\" data-lineheight=\"48px\"><span class=\"ez-toc-section\" id=\"How_the_change_applies_in_Switzerland\"><\/span>How the change applies in Switzerland<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Previously, Switzerland referenced Regulation (EU) 207\/2012 via <a href=\"https:\/\/www.fedlex.admin.ch\/eli\/cc\/2020\/552\/en#annex_3\" target=\"_blank\" rel=\"noopener noreferrer\"><b>Annex 3<\/b><\/a> number 1.2 of the Medical Devices Ordinance (MedDO, SR 812.213). <a href=\"https:\/\/www.fedlex.admin.ch\/eli\/cc\/2020\/552\/en#art_95\" target=\"_blank\" rel=\"noopener noreferrer\"><b>Article 95(2)<\/b><\/a> MedDO stipulated continued application of that EU regulation until a new Implementing Regulation was adopted.<\/p>\n<p>Swissmedic applies EU Commission Implementing Regulations directly under Article 95(1) MedDO. As a result, both Implementing <a href=\"https:\/\/eur-lex.europa.eu\/eli\/reg_impl\/2021\/2226\/oj\/eng\" target=\"_blank\" rel=\"noopener noreferrer\">Regulation (EU) 2021\/2226<\/a> and the amended <a href=\"https:\/\/eur-lex.europa.eu\/eli\/reg_impl\/2025\/1234\/oj\/eng\" target=\"_blank\" rel=\"noopener noreferrer\">Regulation (EU) 2025\/1234<\/a> now apply in Switzerland immediately and without further amendment to the MedDO.<\/p>\n<h2 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 40; line-height: 1.2;\" data-fontsize=\"40\" data-lineheight=\"48px\"><span class=\"ez-toc-section\" id=\"Impact_on_manufacturers\"><\/span>Impact on manufacturers<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>The adoption of Regulation (EU) 2025\/1234 in Switzerland introduces several practical implications for manufacturers:<\/p>\n<h3 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 32; line-height: 1.4;\" data-fontsize=\"32\" data-lineheight=\"44.799999px\"><span class=\"ez-toc-section\" id=\"1_Broader_use_of_e-IFUs_for_professional_users\"><\/span>1. Broader use of e-IFUs for professional users<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>Manufacturers may now provide instructions exclusively in electronic form for all devices intended for professionals, including accessories and Annex XVI products. This change can reduce printing costs and support sustainability initiatives.<\/p>\n<h3 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 32; line-height: 1.4;\" data-fontsize=\"32\" data-lineheight=\"44.799999px\"><span class=\"ez-toc-section\" id=\"2_Mandatory_registration_of_the_e-IFU_address\"><\/span>2. Mandatory registration of the e-IFU address<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>Companies must submit to Eudamed\u2019s UDI database the stable internet address where the e-IFU is accessible. Ensuring uptime, security and version control for that hosting location becomes a regulatory requirement.<\/p>\n<h3 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 32; line-height: 1.4;\" data-fontsize=\"32\" data-lineheight=\"44.799999px\"><span class=\"ez-toc-section\" id=\"3_Clear_user_segmentation_and_labelling\"><\/span>3. Clear user segmentation and labelling<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>Because e-IFUs are permitted only for professional users, manufacturers must implement reliable mechanisms to distinguish professional from lay-user channels. Labelling, sales channels and packaging should clearly indicate when a device requires a paper IFU for lay users.<\/p>\n<h3 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 32; line-height: 1.4;\" data-fontsize=\"32\" data-lineheight=\"44.799999px\"><span class=\"ez-toc-section\" id=\"4_Operational_and_technical_responsibilities\"><\/span>4. Operational and technical responsibilities<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>Manufacturers need robust technical and operational processes to guarantee continuous access to e-IFUs, including:<\/p>\n<ul>\n<li>redundant hosting and monitoring;<\/li>\n<li>access control where required (e.g., professional portals);<\/li>\n<li>document versioning and audit trails;<\/li>\n<li>data protection and cybersecurity measures for hosted content.<\/li>\n<\/ul>\n<h3 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 32; line-height: 1.4;\" data-fontsize=\"32\" data-lineheight=\"44.799999px\"><span class=\"ez-toc-section\" id=\"5_Harmonised_compliance_across_EU_and_Switzerland\"><\/span>5. Harmonised compliance across EU and Switzerland<span class=\"ez-toc-section-end\"><\/span><\/h3>\n<p>Alignment with EU rules simplifies cross-border regulatory strategies. Companies that already follow the EU provisions will find compliance in Switzerland more straightforward, reducing administrative overhead for market access.<\/p>\n<h2 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 40; line-height: 1.2;\" data-fontsize=\"40\" data-lineheight=\"48px\"><span class=\"ez-toc-section\" id=\"What_stakeholders_should_do_next\"><\/span>What stakeholders should do next<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Manufacturers and authorised representatives should review their IFU distribution practices and hosting arrangements. Specifically, they should:<\/p>\n<ol>\n<li>identify devices intended for professional users and confirm eligibility for e-IFUs;<\/li>\n<li>register the e-IFU internet address in <a href=\"https:\/\/health.ec.europa.eu\/medical-devices-eudamed\/udidevice-registration_en\" target=\"_blank\" rel=\"noopener noreferrer\">Eudamed\u2019s UDI<\/a> database as required;<\/li>\n<li>ensure clear labelling and instructions for lay users who must still receive paper IFUs;<\/li>\n<li>implement technical measures for reliable access, version control and security;<\/li>\n<li>update internal procedures and quality documentation to reflect the new obligations.<\/li>\n<\/ol>\n<h2 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 40; line-height: 1.2;\" data-fontsize=\"40\" data-lineheight=\"48px\"><span class=\"ez-toc-section\" id=\"Conclusion\"><\/span>Conclusion<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Swissmedic\u2019s adoption of Implementing <a href=\"https:\/\/eur-lex.europa.eu\/eli\/reg_impl\/2025\/1234\/oj\/eng\" target=\"_blank\" rel=\"noopener noreferrer\">Regulation (EU) 2025\/1234<\/a> brings Switzerland into line with the EU on the electronic provision of instructions for use. The change widens the scope for e-IFUs intended for professional users and clarifies obligations for manufacturers. It also underscores the growing importance of resilient digital infrastructure and clear user segmentation in regulatory compliance.<\/p>\n<h2 class=\"fusion-responsive-typography-calculated\" style=\"--fontsize: 40; line-height: 1.2;\" data-fontsize=\"40\" data-lineheight=\"48px\"><span class=\"ez-toc-section\" id=\"Reference_and_call_to_action\"><\/span>Reference and call to action<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>For full details, consult Swissmedic\u2019s official communication on the implementation of <a href=\"https:\/\/eur-lex.europa.eu\/eli\/reg_impl\/2025\/1234\/oj\/eng\" target=\"_blank\" rel=\"noopener noreferrer\">Regulation (EU) 2025\/1234<\/a> and the text of the implementing regulation. If you would like, we can help prepare a compliance checklist or a draft update to your technical documentation and hosting policy.<\/p>\n<\/article>\n<\/div><div style=\"text-align:center;\"><a class=\"fusion-button button-flat fusion-button-default-size button-default fusion-button-default button-1 fusion-button-default-span fusion-button-default-type\" style=\"--button_margin-top:10px;--button_margin-bottom:20px;\" target=\"_blank\" rel=\"noopener noreferrer\" href=\"https:\/\/cmcmedicaldevices.com\/contact\/\"><span class=\"fusion-button-text\">Contact us today<\/span><\/a><\/div><div class=\"fusion-image-element \" style=\"text-align:center;--awb-max-width:600px;--awb-caption-title-font-family:var(--h2_typography-font-family);--awb-caption-title-font-weight:var(--h2_typography-font-weight);--awb-caption-title-font-style:var(--h2_typography-font-style);--awb-caption-title-size:var(--h2_typography-font-size);--awb-caption-title-transform:var(--h2_typography-text-transform);--awb-caption-title-line-height:var(--h2_typography-line-height);--awb-caption-title-letter-spacing:var(--h2_typography-letter-spacing);\"><span class=\" fusion-imageframe imageframe-none imageframe-1 hover-type-none\"><img decoding=\"async\" width=\"1640\" height=\"924\" title=\"Swissmedic new guidance\" src=\"https:\/\/cmcmedicaldevices.com\/wp-content\/uploads\/2025\/09\/Swissmedic-new-guidance-.png\" alt class=\"img-responsive wp-image-4248\" srcset=\"https:\/\/cmcmedicaldevices.com\/wp-content\/uploads\/2025\/09\/Swissmedic-new-guidance--200x113.png 200w, https:\/\/cmcmedicaldevices.com\/wp-content\/uploads\/2025\/09\/Swissmedic-new-guidance--400x225.png 400w, https:\/\/cmcmedicaldevices.com\/wp-content\/uploads\/2025\/09\/Swissmedic-new-guidance--600x338.png 600w, https:\/\/cmcmedicaldevices.com\/wp-content\/uploads\/2025\/09\/Swissmedic-new-guidance--800x451.png 800w, https:\/\/cmcmedicaldevices.com\/wp-content\/uploads\/2025\/09\/Swissmedic-new-guidance--1200x676.png 1200w, https:\/\/cmcmedicaldevices.com\/wp-content\/uploads\/2025\/09\/Swissmedic-new-guidance-.png 1640w\" sizes=\"(max-width: 640px) 100vw, 1200px\" \/><\/span><\/div><\/div><\/div><\/div><\/div>\n\n\n<div class=\"kk-star-ratings kksr-auto kksr-align-center kksr-valign-bottom\"\n    data-payload='{&quot;align&quot;:&quot;center&quot;,&quot;id&quot;:&quot;4252&quot;,&quot;slug&quot;:&quot;default&quot;,&quot;valign&quot;:&quot;bottom&quot;,&quot;ignore&quot;:&quot;&quot;,&quot;reference&quot;:&quot;auto&quot;,&quot;class&quot;:&quot;&quot;,&quot;count&quot;:&quot;7&quot;,&quot;legendonly&quot;:&quot;&quot;,&quot;readonly&quot;:&quot;&quot;,&quot;score&quot;:&quot;5&quot;,&quot;starsonly&quot;:&quot;&quot;,&quot;best&quot;:&quot;5&quot;,&quot;gap&quot;:&quot;5&quot;,&quot;greet&quot;:&quot;Rate this&quot;,&quot;legend&quot;:&quot;5\\\/5 - (7 votos)&quot;,&quot;size&quot;:&quot;24&quot;,&quot;title&quot;:&quot;Switzerland adopts EU rules on electronic instructions for use for medical devices&quot;,&quot;width&quot;:&quot;142.5&quot;,&quot;_legend&quot;:&quot;{score}\\\/{best} - ({count} {votes})&quot;,&quot;font_factor&quot;:&quot;1.25&quot;}'>\n            \n<div class=\"kksr-stars\">\n    \n<div class=\"kksr-stars-inactive\">\n            <div class=\"kksr-star\" data-star=\"1\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"2\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"3\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"4\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"5\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n    <\/div>\n    \n<div class=\"kksr-stars-active\" style=\"width: 142.5px;\">\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n    <\/div>\n<\/div>\n                \n\n<div class=\"kksr-legend\" style=\"font-size: 19.2px;\">\n            5\/5 - (7 votos)    <\/div>\n    <\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"gallery","meta":{"_acf_changed":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-4252","post","type-post","status-publish","format-gallery","hentry","category-sin-categorizar","post_format-post-format-gallery"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.3.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Switzerland Implements EU Regulation on Electronic Instructions for Use of Medical Devices<\/title>\n<meta name=\"description\" content=\"Swissmedic has adopted EU Implementing Regulation (EU) 2025\/1234 on electronic instructions for use with immediate effect. Professional users in Switzerland can now access e-IFUs for all medical devices, accessories, Annex XVI products, and legacy devices, aligning Swiss rules with the EU MDR.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/cmcmedicaldevices.com\/es\/switzerland-adopts-eu-rules-on-electronic-instructions-for-use-for-medical-devices\/\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Switzerland Implements EU Regulation on Electronic Instructions for Use of Medical Devices\" \/>\n<meta property=\"og:description\" content=\"Swissmedic has adopted EU Implementing Regulation (EU) 2025\/1234 on electronic instructions for use with immediate effect. 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