Statistique de ADRANOX

63Dispositifs total

24UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

2Pays

Santé des certificats de ADRANOX

Aucun certificat enregistré pour ce fabricant.

Aucun dispositif enregistré pour ce fabricant.

Dispositifs placés dans 2 pays

Mise à jour EUDAMED : le 6 mars 2024

IT-MF-000027181

Actif

Nom: Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico
SRN: IT-CA-070
Téléphone: +39 06 5994 3199/ +39 06 5994 3207
Email: segr.dgfdm@sanita.it

BACCHI Raffaele
the conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before a device is released; the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the PMS obligations are complied with in accordance with Article10(10); the reporting obligations referred to in Articles87 to91 are fulfilled; in the case of investigational devices, the statement referred to in Section4.1 of ChapterII of AnnexXV
Masqué