{"id":163,"date":"2021-11-08T16:07:00","date_gmt":"2021-11-08T14:07:00","guid":{"rendered":"https:\/\/new.ehealthpass.eu\/?p=163"},"modified":"2021-11-08T16:07:00","modified_gmt":"2021-11-08T14:07:00","slug":"ehealthpass-earns-the-ce-mark-certification-as-medical-device-software","status":"publish","type":"post","link":"https:\/\/ehealthpass.eu\/el\/ehealthpass-earns-the-ce-mark-certification-as-medical-device-software\/","title":{"rendered":"eHealthPass earns the CE mark certification as medical device software"},"content":{"rendered":"<p><span data-contrast=\"auto\">The CE marking allows the manufacturer to freely circulate their product throughout the countries of the European Economic Area (EEA).\u00a0The great benefit for\u00a0them\u00a0is that there is now only one set of requirements and procedures to comply with in designing and manufacturing a product for the entire EEA. The various and conflicting national regulations are eliminated. As a result, the product no longer needs to be adapted to the specific requirements of the different member states of the EEA.\u00a0In addition, by implementing these\u00a0requirements the product will be safer for the user and this also reduces\u00a0damage and liability claims.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:259}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">The\u00a0Medical Device Directive (93\/42\/EEC), according to which our platform is certified,\u00a0applies to medical devices and their accessories placed in the EU market. Medical devices are defined as any instrument, apparatus, appliance, software, implant, reagent,\u00a0material,\u00a0or another article intended to be used for medical purposes, such as\u00a0medical diagnosis\u00a0&amp; disease\u00a0monitoring.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:259}\">\u00a0<\/span><\/p>\n<p><a href=\"https:\/\/www.gnomon.com.gr\/ehealthpass\/\"><b><span data-contrast=\"auto\">eHealthPass<\/span><\/b><b><span data-contrast=\"auto\">TM<\/span><\/b><\/a><span data-contrast=\"auto\">\u00a0is\u00a0a multifunctional platform for family health and disease management. It provides health records\u2019 access, information sharing with professionals, treatment planning and monitoring, emergency support, with a focus on patient consent and privacy, and alerting of any abnormal situation as it is defined by health care professionals, using international and open interoperability standards.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:259}\">\u00a0<\/span><\/p>\n<p><span data-contrast=\"auto\">Therefore,\u00a0<\/span><a href=\"https:\/\/www.gnomon.com.gr\/ehealthpass\/\"><b><span data-contrast=\"auto\">eHealthPass<\/span><\/b><b><span data-contrast=\"auto\">TM<\/span><\/b><\/a><span data-contrast=\"auto\">\u00a0platform\u00a0can move freely between the member states.\u00a0As such, CE Marking can be seen as\u00a0\u201cpassport\u201d\u00a0for the European marketplace.\u00a0This is also an identifier that our platform has\u00a0a high level of health,\u00a0safety\u00a0and environmental protection, as\u00a0it\u00a0meets\u00a0the requirements of the European Directives.\u00a0Our company\u00a0complies\u00a0with the requirements of the directives\u00a0and\u00a0has taken account of the current state-of-the-art procedures.\u00a0Users of CE marked\u00a0eHealthPass<\/span><span data-contrast=\"auto\">TM<\/span><span data-contrast=\"auto\">\u00a0platform\u00a0enjoy the same level of protection.<\/span><span data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335551550&quot;:6,&quot;335551620&quot;:6,&quot;335559739&quot;:160,&quot;335559740&quot;:259}\">\u00a0<\/span><\/p>\n<div class=\"blog-share text-center\"><\/div>","protected":false},"excerpt":{"rendered":"<p>The CE marking allows the manufacturer to freely circulate their product throughout the countries of the European Economic Area (EEA).\u00a0The great benefit for\u00a0them\u00a0is that there is now only one set of requirements and procedures to comply with in designing and manufacturing a product for the entire EEA. The various and conflicting national regulations are eliminated&#8230;.<\/p>","protected":false},"author":1,"featured_media":158,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"inline_featured_image":false,"footnotes":""},"categories":[3],"tags":[],"class_list":["post-163","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-news"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>eHealthPass earns the CE mark certification as medical device software &#8226; eHealthPass<\/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:\/\/ehealthpass.eu\/el\/ehealthpass-earns-the-ce-mark-certification-as-medical-device-software\/\" \/>\n<meta property=\"og:locale\" content=\"el_GR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"eHealthPass earns the CE mark certification as medical device software &#8226; eHealthPass\" \/>\n<meta property=\"og:description\" content=\"The CE marking allows the manufacturer to freely circulate their product throughout the countries of the European Economic Area (EEA).\u00a0The great benefit for\u00a0them\u00a0is that there is now only one set of requirements and procedures to comply with in designing and manufacturing a product for the entire EEA. 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