{"id":8456,"date":"2025-09-03T03:19:35","date_gmt":"2025-09-02T19:19:35","guid":{"rendered":"https:\/\/www.neoss.com\/sv\/?post_type=news&#038;p=8456"},"modified":"2025-09-03T03:20:51","modified_gmt":"2025-09-02T19:20:51","slug":"alla-neoss-groups-produkter-ar-certifieradeenligt-eu-medical-device-regulation-mdr","status":"publish","type":"news","link":"https:\/\/www.neoss.com\/sv\/news\/alla-neoss-groups-produkter-ar-certifieradeenligt-eu-medical-device-regulation-mdr\/","title":{"rendered":"Alla Neoss\u00ae Groups produkter \u00e4r certifierade enligt EU Medical Device Regulation (MDR)"},"content":{"rendered":"\n<p>Neoss Group \u00e4r stolta \u00f6ver att vi \u00e4r certifierade enligt EU Medical Device Regulation (MDR) fr\u00e5n v\u00e5r notified body, BSI Group Netherlands BV, f\u00f6r samtliga produkter i sortimentet.<\/p>\n\n\n\n<p>Neoss Group \u00e4r stolta \u00f6ver att hela f\u00f6retagets produktportf\u00f6lj \u00e4r certifierad enligt EU:s medicintekniska f\u00f6rordning MDR (EU 2017\/745), genom det anm\u00e4lda organet BSI Group. Certifieringen omfattar samtliga implantat, abutments och tillh\u00f6rande komponenter i Neoss system.<\/p>\n\n\n\n<p>\u201cDetta \u00e4r ett viktigt bevis p\u00e5 v\u00e5rt l\u00e5ngsiktiga \u00e5tagande f\u00f6r kvalitet, patients\u00e4kerhet och transparens\u201d, s\u00e4ger Albin Wahlstrand, VD f\u00f6r Neoss Norden. \u201cVi v\u00e4lkomnar den h\u00f6ga standard som MDR kr\u00e4ver, och \u00e4r stolta \u00f6ver att uppfylla \u2013 och i m\u00e5nga fall \u00f6vertr\u00e4ffa \u2013 de regulatoriska kraven.\u201d<\/p>\n\n\n\n<p>Om certifieringen<br>Den nya medicintekniska f\u00f6rordningen (MDR) st\u00e4ller betydligt h\u00f6gre krav p\u00e5 dokumentation, klinisk evidens, sp\u00e5rbarhet och eftermarknadskontroll \u00e4n tidigare regelverk (MDD). Certifiering via BSI, ett av Europas mest erfarna anm\u00e4lda organ, inneb\u00e4r att Neoss produkter har granskats i detalj och bed\u00f6mts som fullt f\u00f6renliga med den nya f\u00f6rordningen.<\/p>\n\n\n\n<p>Certifieringen omfattar bland annat:<br>\u2022 Neoss implantatsystem<br>\u2022 Protetiska komponenter och abutments<br>\u2022 Tillh\u00f6rande kirurgiska instrument och tillbeh\u00f6r<br>\u2022 Icke resorberbara membran \u2013 NeoGen PTFE<\/p>\n\n\n\n<p>Fokus p\u00e5 patients\u00e4kerhet och transparens<br>Neoss har sedan starten arbetat utifr\u00e5n principen att f\u00f6renkla det komplexa \u2013 utan att kompromissa med s\u00e4kerheten. MDR-certifieringen \u00e4r ytterligare ett kvitto p\u00e5 att Neoss system \u00e4r utformat f\u00f6r att leverera tillf\u00f6rlitliga och kliniskt bepr\u00f6vade l\u00f6sningar.<\/p>\n\n\n\n<p>\u201cVi kommer forts\u00e4tta arbeta n\u00e4ra v\u00e5ra kunder och partners f\u00f6r att s\u00e4kerst\u00e4lla att varje produkt vi levererar uppfyller de h\u00f6gsta kraven inom modern implantologi\u201d, s\u00e4ger Albin Wahlstrand.<\/p>\n\n\n\n<p>Har du som kund fr\u00e5gor eller funderingar \u00e4r du alltid v\u00e4lkommen att kontakta oss p\u00e5 Neoss.<br>F\u00f6r mer information om v\u00e5ra certifikat, produktdokumentation eller regulatorisk efterlevnad,<br>bes\u00f6k neoss.com\/sv\/certifikat\/<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Neoss Group \u00e4r stolta \u00f6ver att vi \u00e4r certifierade enligt EU Medical Device Regulation (MDR) fr\u00e5n v\u00e5r notified body, BSI Group Netherlands BV, f\u00f6r samtliga produkter i sortimentet. Neoss Group \u00e4r stolta \u00f6ver att hela f\u00f6retagets produktportf\u00f6lj \u00e4r certifierad enligt EU:s medicintekniska f\u00f6rordning MDR (EU 2017\/745), genom det anm\u00e4lda organet BSI Group. Certifieringen omfattar samtliga [&hellip;]<\/p>\n","protected":false},"featured_media":8459,"template":"","meta":{"_acf_changed":false,"content-type":"","_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":""},"topic":[],"class_list":["post-8456","news","type-news","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v24.8 (Yoast SEO v24.8.1) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Alla Neoss\u00ae Groups produkter \u00e4r certifierade enligt EU Medical Device Regulation (MDR) - Sverige<\/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.neoss.com\/sv\/news\/alla-neoss-groups-produkter-ar-certifieradeenligt-eu-medical-device-regulation-mdr\/\" \/>\n<meta property=\"og:locale\" content=\"sv_SE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Alla Neoss\u00ae Groups produkter \u00e4r certifierade enligt EU Medical Device Regulation (MDR)\" \/>\n<meta property=\"og:description\" content=\"Neoss Group \u00e4r stolta \u00f6ver att vi \u00e4r certifierade enligt EU Medical Device Regulation (MDR) fr\u00e5n v\u00e5r notified body, BSI Group Netherlands BV, f\u00f6r samtliga produkter i sortimentet. Neoss Group \u00e4r stolta \u00f6ver att hela f\u00f6retagets produktportf\u00f6lj \u00e4r certifierad enligt EU:s medicintekniska f\u00f6rordning MDR (EU 2017\/745), genom det anm\u00e4lda organet BSI Group. 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