{"id":19706,"date":"2021-12-14T11:24:55","date_gmt":"2021-12-14T10:24:55","guid":{"rendered":"https:\/\/www.thema-med.com\/?p=19706"},"modified":"2021-12-14T11:24:55","modified_gmt":"2021-12-14T10:24:55","slug":"for-which-medical-devices-is-it-necessary-appoint-ch-rep","status":"publish","type":"post","link":"https:\/\/www.thema-med.com\/en\/2021\/12\/14\/for-which-medical-devices-is-it-necessary-appoint-ch-rep\/","title":{"rendered":"For which Medical Devices is it necessary to appoint a Swiss Authorised Representative?"},"content":{"rendered":"\n<p>The designation of the Swiss Authorised Representative (CH REP) is required to market all Medical Devices, <strong>including legacy devices<\/strong>, i.e. devices covered by a certificate still valid in compliance with the MDD \/ AIMDD Directives and class I devices that will require the intervention of a Notified Body (ON) which can continue to be made available on the market or put into service until May 27, 2025.<\/p>\n\n\n<p><strong><a href=\"https:\/\/www.thema-med.com\/en\/services\/\">Discover the strategic-regulatory consultancy services Thema<\/a><\/strong><br><!--StartFragment--><\/p>\n\n\n<h2 class=\"wp-block-heading\"><strong>THEMA SWISS NEWS<\/strong><\/h2>\n\n\n\n<p>Do you want to stay updated on the main news regarding the Switzerland \u2013 EU Agreement in the field of Medical Devices?<\/p>\n\n\n\n<p>Fill out the form and receive periodically our THEMA: SWISS NEWS by email!<\/p>\n\n\n<p class=\"wpcf7-contact-form-not-found\"><strong>Error:<\/strong> Contact form not found.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The designation of the Swiss Authorised Representative (CH REP) is required to market all Medical Devices, including legacy devices, i.e. devices  [&#8230;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[892,1448],"tags":[],"class_list":["post-19706","post","type-post","status-publish","format-standard","hentry","category-faq-en","category-switzerland-faq-en"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.0 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>For which Medical Devices is it necessary to appoint a CH REP?<\/title>\n<meta name=\"description\" content=\"The designation of the Swiss Authorised Representative (CH REP) is required to market all Medical Devices, including legacy devices\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, 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