{"id":9729,"date":"2019-06-12T09:20:13","date_gmt":"2019-06-12T07:20:13","guid":{"rendered":"http:\/\/www.thema-med.com\/?p=9729"},"modified":"2019-06-12T09:20:13","modified_gmt":"2019-06-12T07:20:13","slug":"how-can-i-continue-to-sell-my-devices-after-the-full-implementation-of-mdr","status":"publish","type":"post","link":"https:\/\/www.thema-med.com\/en\/2019\/06\/12\/how-can-i-continue-to-sell-my-devices-after-the-full-implementation-of-mdr\/","title":{"rendered":"How can I continue to sell my devices after the full implementation of MDR?"},"content":{"rendered":"\n

The MDR certificate is a new certification<\/strong> and not an amendment of the Medical Device Directive (MDD) 93\/42\/EEC. However, pending the obtaining of a certificate of conformity pursuant to MDR, a medical device can continue to be marketed if it holds a valid CE certificate issued under MDD.<\/p>\n\n\n\n

A CE MDD certificate will remain valid until its natural expiry date even after May 26, 2021 (the date of full implementation of the MDR (EU) 2017\/745), provided that, starting 2020, the manufacturer already demonstrates compliance during the audit phase to the MDR post-market surveillance<\/strong>, market surveillance, vigilance<\/strong> and registration<\/strong> of the Manufacturer and economic operators requirements.<\/p>\n\n\n\n

Questions? Request more info from our specialists 
CONTACT US<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

The MDR certificate is a new certification and not an amendment of the Medical Device Directive (MDD) 93\/42\/EEC. However, pending the […]<\/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":[892,1554],"tags":[],"class_list":["post-9729","post","type-post","status-publish","format-standard","hentry","category-faq-en","category-mdr-impact-ce-mdd-certificates-period-of-grace"],"acf":[],"yoast_head":"\nHow can I continue to sell my devices after the full implementation of MDR? - Thema Med<\/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:\/\/www.thema-med.com\/en\/2019\/06\/12\/how-can-i-continue-to-sell-my-devices-after-the-full-implementation-of-mdr\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"How can I continue to sell my devices after the full implementation of MDR? - Thema Med\" \/>\n<meta property=\"og:description\" content=\"The MDR certificate is a new certification and not an amendment of the Medical Device Directive (MDD) 93\/42\/EEC. 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