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EUDAMED database - EUDAMED - European Commission
- https://ec.europa.eu/tools/eudamed/
- The creation of a European database on medical devices (EUDAMED) is one of the key aspects of the new rules on medical devices ( Regulation (EU) 2017/745) and in vitro …
Medical Devices - EUDAMED - Public Health
- https://health.ec.europa.eu/medical-devices-eudamed_en
- EUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746… Actors …
MDR-Eudamed - Europa
- https://webgate.ec.europa.eu/eudamed/landing-page
- MDR EUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro …
EUDAMED European Database for Medical …
- https://www.bsigroup.com/en-US/medical-devices/Global-market-access/European-market-access/eudamed/
- The European Database on Medical Devices ( EUDAMED) is the IT system developed by the European Commission as an integral part of MDR and IVDR implementation. It aims …
European database on medical devices (EUDAMED)
- https://www.medtecheurope.org/news-and-events/news/european-database-on-medical-devices-eudamed/
- European database on medical devices (EUDAMED) The European Commission has recently set up a new webpage to collect information that is related to …
EUDAMED Database - Progress Updates - MEDIcept
- https://www.medicept.com/2022/06/24/eudamed-database-progress-updates/
- The European Database for Medical Devices, or EUDAMED, is intended to store and provide information on the manufacture, distribution, certification, and post …
Preparing for EUDAMED - Europe’s Medical …
- https://www.greenlight.guru/blog/eudamed-europe-medical-device-database
- The Medical Devices Regulation 2017/745 (MDR) and In Vitro Diagnostics Regulation 2017/746 (IVDR) replace the existing directives and are legally-binding …
MDCG 2020-19
- https://mdi-europa.com/wp-content/uploads/2023/02/mdcg_2022-19_en.pdf
- EUDAMED European database on medical devices GSPR General safety and performance requirements NCA National competent authority PMPF Post-market …
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