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17 maj 2024 · The European Medical Device Nomenclature (EMDN) is the nomenclature of use by manufacturers when registering their medical devices in the EUDAMED database.
Per Article 26 of Regulation (EU) 2017/745 on medical devices (MDR) and Article 23 of Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR), the European Medical Device Nomenclature (EMDN) aims at supporting the functioning of the European database on medical devices (EUDAMED).
4 cze 2021 · Per Article 26 of Regulation (EU) 2017/745 on medical devices (MDR) and Article 23 of Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR), the European Medical Device Nomenclature (EMDN) aims at supporting the functioning of the European database on medical devices (EUDAMED).
See “EFPIA & GS1: a shared vision for product identification in the context of the EU Directive on Falsified Medicines”, issued January 2012. Content of the 2D Code. The recommendation for coding of pharmaceutical products is to encode in a Data Matrix code a minimum of four items of data.
4 cze 2021 · Latest updates. FAQ on the European Medical Device Nomenclature (EMDN) News announcement. 4 June 2021. Directorate-General for Health and Food Safety. 1 min read.
The national medicine registers in the different Member States of the European Union (EU) and European Economic Area (EEA) contain information on medicines authorised in those countries, including links for the summary of product characteristics (SmPC) and the package leaflet.
The purpose of this practical guide is to provide members of the Joint Sickness Insurance Scheme of the European Union institutions (the JSIS) with an easy-to-use summary of the rules for the reimbursement of medical expenses (General implementing provisions), which entered into force on 1 July 2007.
