Áttekintés A következő új jogszabályok lesznek alkalmazandók az EU-ban:2021. május 26-tól: az orvostechnikai eszközökről szóló (EU) 2017/745 rendelet2022. május… FelkészülésManufacturer IVDManufacturers MDManufacturers of devices without an intended medical purposeHealthcare professionals and health institutionsThe procurement of MDs and IVDsAuthorised Representatives, Importers and DistributorsCompetent authorities in non-EU/EEA countriesÚtmutatók Az Európai Bizottság egy sor útmutató dokumentumot tett közzé, amelyek segítik az érdekelt feleket az orvostechnikai eszközökről szóló rendeletek… Latest updatesNews announcement | 21 június 2022Setting the scene for EU reference labs for high-risk diagnosticsNews announcement | 24 május 2022Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for in vitro diagnostic medical devicesNews announcement | 13 április 2022Notice to Stakeholders: EU-Turkey Customs Union Agreement in the field of medical devicesNews announcement | 1 április 2022Update - Joint implementation and preparedness plan for Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR)Összes megtekintése HighlightsNews announcement | 21 június 2022Setting the scene for EU reference labs for high-risk diagnostics26 May 2022, the Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices is applicable within the EUNews announcement | 26 május 2021Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for medical devicesGeneral publications | 10 július 2020State of play of Joint implementation Plan on actions considered necessary to ensure the sound functioning of the new framework for medical devices under the MDRThe UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI systemGetting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activitiesCommission Notice on notified bodies’ audits performed during Covid-19 exceptional circumstancesGeneral publications | 15 július 2020Factsheet on MDR requirements for Transparency and Public Information Events07máj.2021 Partneri találkozók Webinar for Patients – Safe and performant Medical Devices for all DocumentsEventsPublications
News announcement | 24 május 2022Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for in vitro diagnostic medical devices
News announcement | 13 április 2022Notice to Stakeholders: EU-Turkey Customs Union Agreement in the field of medical devices
News announcement | 1 április 2022Update - Joint implementation and preparedness plan for Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR)
26 May 2022, the Regulation (EU) 2017/746 on In Vitro Diagnostic Medical Devices is applicable within the EU
News announcement | 26 május 2021Notice to Stakeholders: Status of the EU-Switzerland Mutual Recognition Agreement (MRA) for medical devices
General publications | 10 július 2020State of play of Joint implementation Plan on actions considered necessary to ensure the sound functioning of the new framework for medical devices under the MDR
The UDI Helpdesk is live. It helps the economic operators in the implementation of the requirements introduced by the new UDI system
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
General publications | 15 július 2020Factsheet on MDR requirements for Transparency and Public Information
