Skip to main content
Home - European Commission
Français
fr
Dialog
Select your language
Български
Čeština
Dansk
Deutsch
Eesti
Ελληνικά
English
Español
Français
Hrvatski
Gaeilge
Italiano
Latviešu
Lietuvių
Magyar
Malti
Nederlands
Polski
Português
Română
Suomi
Slovenčina
Slovenščina
Svenska
Close
Search this website
Recherche
Accueil
Vivre, travailler et voyager dans l’UE
Santé publique
Medical Devices - Topics of Interest
Medical Devices - Topics of Interest
Tous les thèmes
Aperçu général
Organismes notifiés
Identifiant unique des dispositifs (IUD)
Retraitement
Gérer la santé publique dans l'UE
Stratégie en matière de santé
State of Health in the EU
Santé et fonds structurels
L'UE dans le monde
Indicateurs de santé
Améliorer les systèmes de santé
Soins transfrontaliers
European Reference Networks
Santé en ligne
Évaluation des technologies de la santé
Personnel de santé
Health systems performance assessment
Expert Panel on effective ways of investing in health
Promouvoir la santé
Tabac
Alimentation et activité physique
Alcool
Déterminants sociaux et inégalités en matière de santé
Medical devices
Medical Devices - Sector
Medical Devices - New regulations
Medical Devices - Topics of Interest
Medical Devices - Dialogue between interested parties
Medical Devices - Expert Panels
Medical Devices - EUDAMED
Substances of human origin
Sang, tissus et organes
Produits pharmaceutiques
Médicaments à usage humain
EudraLex
Union Register
Pharmaceutical committee and expert groups
European Medicines Agency (EMA)
Agir contre les maladies
Health security and infectious diseases
European Centre for Disease Prevention and Control (ECDC)
Vaccination
Résistance aux antimicrobiens
Maladies graves et chroniques
Cancer
Évaluation des risques
Comités scientifiques
Endocrine disruptors
Endocrine disruptors
Biocides
Biocides
Dernières mises à jour
23 Mars 2021
Infographic - Is your software a Medical Device?
08 Mars 2021
Updated version - Information on the applications for designation as a notified body (short overview)
18 Janvier 2021
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
11 Janvier 2021
Covid-19: Commission Notice on audits to be performed by notified bodies
11 Décembre 2020
Updated presentation - Information on the applications for designation as a notified body under Regulations (EU) 2017/745 and 2017/746
01 Décembre 2020
The EUDAMED Actor module is in production. On 1st December 2020 the European Commission has made available the Actor registration module to Member States and economic operators
20 Octobre 2020
New web page with the basic information on the EUDAMED Actor registration module
13 Juillet 2020
Survey on availability and capacity of notified bodies to carry out conformity assessments for COVID-19 essential devices
12 Juillet 2020
Amendment to Implementing Regulation 920/2013 on the designation of notified bodies
12 Juillet 2020
MDCG 2020-11: Guidance on the renewal of designation and monitoring of notified bodies
Pages
1
2
next ›
last »
Bulletin d'information
Bulletin d'information
Bulletin d'information
Wed, 03/31/2021
La Commission soutient la transparence avec un nouveau règlement relatif à l’alimentation
Dernières mises à jour
Infographic - Is your software a Medical Device?
Publié
23 Mars 2021
Updated version - Information on the applications for designation as a notified body (short overview)
Publié
08 Mars 2021
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
Publié
18 Janvier 2021
Suivez-nous sur Twitter
En savoir plus
À la une
Getting ready for the new medical devices regulations – Factsheets on the main areas of the medical devices sector activities
Commission Notice on notified bodies’ audits performed during Covid-19 exceptional circumstances
Commission guidelines on Union-wide derogations for medical devices
Informations complémentaires
Publications