{"listableLinks":null,"documentId":34907,"title":"Transition Timelines from the Directives to the Regulations - Medical Devices and in vitro Diagnostic Medical Devices","language":"en","attachments":[{"listableLinks":null,"title":"Transition Timelines from the Directives to the Regulations - Medical Devices and in vitro Diagnostic Medical Devices","language":"EN","nativeRenditionSize":120749,"pdfRenditionSize":119993,"renditionAvailable":true,"version":"1.0","translations":[{"listableLinks":null,"title":"Fristen für den Übergang von den Richtlinien zu den Verordnungen - Medizinprodukte und In-vitro-Diagnostika","language":"DE","nativeRenditionSize":516406,"pdfRenditionSize":494632,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-DE.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/de/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/de/renditions/pdf"}]},{"listableLinks":null,"title":"Aikataulu siirtymiselle direktiiveistä asetuksiin - Lääkinnälliset laitteet ja in vitro -diagnostiikkaan tarkoitetut lääkinnälliset laitteet","language":"FI","nativeRenditionSize":507218,"pdfRenditionSize":485204,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-FI.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/fi/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/fi/renditions/pdf"}]},{"listableLinks":null,"title":"Calendário de transição das diretivas para os regulamentos - Dispositivos Médicos e Dispositivos Médicos de Diagnóstico In Vitro","language":"PT","nativeRenditionSize":493300,"pdfRenditionSize":483763,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-PT.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/pt/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/pt/renditions/pdf"}]},{"listableLinks":null,"title":"График на прехода от директивите към регламентите - Медицински изделия и медицински изделия за инвитро диагностика","language":"BG","nativeRenditionSize":526453,"pdfRenditionSize":535000,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-BG.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/bg/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/bg/renditions/pdf"}]},{"listableLinks":null,"title":"Perėjimo nuo direktyvų prie reglamentų tvarkaraštis - Medicinos priemonės ir in vitro diagnostikos medicinos priemonės","language":"LT","nativeRenditionSize":508915,"pdfRenditionSize":491622,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-LT.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/lt/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/lt/renditions/pdf"}]},{"listableLinks":null,"title":"Vremenske crte – prelazak s direktiva na uredbe - Medicinski proizvodi i in vitro dijagnostički medicinski proizvodi","language":"HR","nativeRenditionSize":490026,"pdfRenditionSize":482312,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-HR.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/hr/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/hr/renditions/pdf"}]},{"listableLinks":null,"title":"Termiņi pārejai no direktīvām uz regulām - Medicīniskas ierīces un in vitro diagnostikas medicīniskās ierīces","language":"LV","nativeRenditionSize":501409,"pdfRenditionSize":486995,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-LV.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/lv/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/lv/renditions/pdf"}]},{"listableLinks":null,"title":"Calendrier de transition des directives aux règlements - Dispositifs médicaux et dispositifs médicaux de diagnostic in vitro","language":"FR","nativeRenditionSize":491453,"pdfRenditionSize":484070,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-FR.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/fr/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/fr/renditions/pdf"}]},{"listableLinks":null,"title":"Az irányelvekről a rendeletekre történő áttérés időrendi áttekintése - Orvostechnikai eszközök és in vitro diagnosztikai orvostechnikai eszközök","language":"HU","nativeRenditionSize":489441,"pdfRenditionSize":484411,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-HU.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/hu/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/hu/renditions/pdf"}]},{"listableLinks":null,"title":"Časová os prechodu od smerníc k nariadeniam - Zdravotnícke pomôcky a diagnostické zdravotnícke pomôcky in vitro","language":"SK","nativeRenditionSize":536200,"pdfRenditionSize":494204,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-SK.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/sk/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/sk/renditions/pdf"}]},{"listableLinks":null,"title":"Časovni razpored prehoda z direktiv na uredbi - Medicinski pripomočki in in vitro diagnostični medicinski pripomočki","language":"SL","nativeRenditionSize":538400,"pdfRenditionSize":498238,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-SL.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/sl/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/sl/renditions/pdf"}]},{"listableLinks":null,"title":"Tidtabell för övergången från direktiven till förordningarna - Medicintekniska produkter och medicintekniska produkter för in vitro-diagnostik","language":"SV","nativeRenditionSize":537249,"pdfRenditionSize":498329,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-SV.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/sv/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/sv/renditions/pdf"}]},{"listableLinks":null,"title":"Χρονοδιαγράμματα μετάβασης από τις οδηγίες στους κανονισμούς - Ιατροτεχυολογικά προϊόντα και in vitro διαγωστικά ιατροτεχνολογικα προϊόντα","language":"EL","nativeRenditionSize":563498,"pdfRenditionSize":513775,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-EL.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/el/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/el/renditions/pdf"}]},{"listableLinks":null,"title":"Skedi ta’ tranżizzjoni mid-Direttivi għar-Regolamenti - Apparati Mediċi u Apparati Mediċi Dijanjostiċi in vitro","language":"MT","nativeRenditionSize":505421,"pdfRenditionSize":486948,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-MT.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/mt/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/mt/renditions/pdf"}]},{"listableLinks":null,"title":"Transition Timelines from the Directives to the Regulations - Medical Devices and in vitro Diagnostic Medical Devices","language":"EN","nativeRenditionSize":120749,"pdfRenditionSize":119993,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-EN.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/en/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/en/renditions/pdf"}]},{"listableLinks":null,"title":"Periodi di transizione dalle direttive ai regolamenti - Dispositivi medici e dispositivi medico-diagnostici in vitro","language":"IT","nativeRenditionSize":492364,"pdfRenditionSize":476878,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-IT.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/it/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/it/renditions/pdf"}]},{"listableLinks":null,"title":"从指令向条例过渡的时间表 医疗器械设备与体外诊断医疗器械设备","language":"ZH","nativeRenditionSize":521617,"pdfRenditionSize":491031,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-ZH.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/zh/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/zh/renditions/pdf"}]},{"listableLinks":null,"title":"Calendario de transición de las Directivas a los Reglamentos - sobre los productos sanitarios y sobre los productos sanitarios para diagnóstico in vitro","language":"ES","nativeRenditionSize":502799,"pdfRenditionSize":485129,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-ES.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/es/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/es/renditions/pdf"}]},{"listableLinks":null,"title":"Üleminek direktiividelt määrustele – tähtajad - Meditsiiniseadmed ja in vitro diagnostika meditsiiniseadmed","language":"ET","nativeRenditionSize":516467,"pdfRenditionSize":492901,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-ET.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/et/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/et/renditions/pdf"}]},{"listableLinks":null,"title":"Lhůty pro přechod ze směrnic na nařízení - Zdravotnické prostředky a diagnostické zdravotnické prostředky in vitro","language":"CS","nativeRenditionSize":548501,"pdfRenditionSize":510847,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-CS.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/cs/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/cs/renditions/pdf"}]},{"listableLinks":null,"title":"Harmonogram przejścia z dyrektyw na rozporządzenia - Wyroby medyczne i wyroby medyczne do diagnostyki in vitro","language":"PL","nativeRenditionSize":514753,"pdfRenditionSize":492499,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-PL.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/pl/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/pl/renditions/pdf"}]},{"listableLinks":null,"title":"Tidslinje for overgangen fra direktiverne til forordningerne Medicinsk udstyr og medicinsk udstyr til in vitro-diagnostik","language":"DA","nativeRenditionSize":509858,"pdfRenditionSize":490591,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-DA.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/da/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/da/renditions/pdf"}]},{"listableLinks":null,"title":"Calendarele de tranziţie de la directive la regulamente - Dispozitive medicale și dispozitive medicale pentru diagnostic in vitro","language":"RO","nativeRenditionSize":566632,"pdfRenditionSize":505178,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-RO.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/ro/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/ro/renditions/pdf"}]},{"listableLinks":null,"title":"Tijdschema voor de overgang van de richtlijnen naar de verordeningen - Medische hulpmiddelen en medische hulpmiddelen voor in-vitrodiagnostiek","language":"NL","nativeRenditionSize":474796,"pdfRenditionSize":475366,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-NL.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/nl/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/nl/renditions/pdf"}]}],"fileName":"INFOGRAPHIC TIMELINE-EN.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/en/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/1/translations/en/renditions/pdf"}]},{"listableLinks":null,"title":"الجداول الزمنیة للمرحلة الانتقالیة من التوجیھات إلى اللوائح الأجھزة الطبیة والأجھزة الطبیة التشخیصیة في المختبر","language":"AU","nativeRenditionSize":652108,"pdfRenditionSize":654133,"renditionAvailable":true,"version":"1.0","translations":[{"listableLinks":null,"title":"الجداول الزمنیة للمرحلة الانتقالیة من التوجیھات إلى اللوائح الأجھزة الطبیة والأجھزة الطبیة التشخیصیة في المختبر","language":"AU","nativeRenditionSize":652108,"pdfRenditionSize":654133,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-AR.PDF","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/3/translations/au/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/3/translations/au/renditions/pdf"}]}],"fileName":"INFOGRAPHIC TIMELINE-AR.PDF","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/3/translations/au/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/3/translations/au/renditions/pdf"}]},{"listableLinks":null,"title":"Сроки перехода от директив к Регламенту о медицинских изделиях и Регламенту о медицинских изделиях для диагностики in vitro","language":"AU","nativeRenditionSize":534810,"pdfRenditionSize":503260,"renditionAvailable":true,"version":"1.0","translations":[{"listableLinks":null,"title":"Сроки перехода от директив к Регламенту о медицинских изделиях и Регламенту о медицинских изделиях для диагностики in vitro","language":"AU","nativeRenditionSize":534810,"pdfRenditionSize":503260,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-RU.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/2/translations/au/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/2/translations/au/renditions/pdf"}]}],"fileName":"INFOGRAPHIC TIMELINE-RU.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/2/translations/au/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/2/translations/au/renditions/pdf"}]},{"listableLinks":null,"title":"指令から規制への移行スケジュール 医療機器および体外診断用医療機器","language":"AU","nativeRenditionSize":483386,"pdfRenditionSize":493813,"renditionAvailable":true,"version":"1.0","translations":[{"listableLinks":null,"title":"指令から規制への移行スケジュール 医療機器および体外診断用医療機器","language":"AU","nativeRenditionSize":483386,"pdfRenditionSize":493813,"renditionAvailable":true,"version":null,"translations":null,"fileName":"INFOGRAPHIC TIMELINE-JP.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/4/translations/au/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/4/translations/au/renditions/pdf"}]}],"fileName":"INFOGRAPHIC TIMELINE-JP.pdf","sortOrder":null,"links":[{"rel":"native","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/4/translations/au/renditions/native"},{"rel":"pdf","href":"https://ec.europa.eu/docsroom/documents/34907/attachments/4/translations/au/renditions/pdf"}]}],"urlRedirect":null,"externalizationDate":1555072427000,"firstExternalizationDate":1555072405000,"lastUpdateDate":1555079598000,"registererService":"grow.a.1.dir","tags":[],"keywords":["medical device","legislation","information","guide"],"links":[{"rel":"self","href":"https://ec.europa.eu/docsroom/documents/34907"}]}