Statistics for ADRANOX

63Total Devices

24Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

2Countries

Certificate health for ADRANOX

No certificates registered for this manufacturer.

No devices registered for this manufacturer.

Devices placed in 2 countries

EUDAMED update: Mar 6, 2024

IT-MF-000027181

Active

Name: Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico
SRN: IT-CA-070
Phone: +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
Hidden