Statistique de EUROMI

4Dispositifs total

3UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

2Pays

Santé des certificats de EUROMI

Aucun certificat enregistré pour ce fabricant.

Affichage de 1–4 sur 4 dispositifs.

Dénomination commerciale	Numéro de référence/catalogue	Code d'UDI-DI	Quantité	Statut
1316INFL-2.5150	`1316INFL-2.5150`	`03701416200745`	1	Sur le marché
1220LSU1B-3200	`1220LSU1B-3200`	`03701416203883`	1	Sur le marché
1118NLF2DH	`1118NLF2DH`	`03701416203555`	1	Sur le marché
1127ADIPC	`1127ADIPC`	`03701416203425`	1	Sur le marché

Dispositifs placés dans 2 pays

Mise à jour EUDAMED : le 13 févr. 2024

BE-MF-000014212

Actif

Adresse: 11, RUE DES NOUVELLES TECHNOLOGIES B-4821 ANDRIMONT, DISON BELGIQUE
Téléphone: +32 87 29 22 22
Email: info@euromi.com
Site web: https://www.euromi.com/fr/

Nom: Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
SRN: BE-CA-007
Téléphone: +32 2 528 40 00
Email: notifications.meddev@fagg-afmps.be

BENOIT Perrine
- Ensure that the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released. - Ensure that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date
Masqué
MASCREZ Olivia
- Ensure that conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before release - Ensure that the technical documentation & EU DoC are drawn up & up-to-date - Ensure that PMS obligations are complied with (Article 10) - Ensure that reporting obligations referred to in Art 87 to 91 are fulfilled - Ensure that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued
Masqué