Statistics for FARMA-DERMA S.r.l.

31Total Devices

6Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

11Countries

Certificate health for FARMA-DERMA S.r.l.

No certificates registered for this manufacturer.

No devices registered for this manufacturer.

Devices placed in 11 countries

EUDAMED update: Feb 14, 2024

IT-MF-000020737

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

MONTORSI Lorena
art. 15 (a) 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; (c) the post-market surveillance obligations are complied with in accordance with Article 10(10); (d) the reporting obligations referred to in Articles 87 to 91 are fulfilled;
Hidden
CORNIA Francesca
art. 15 (b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date;
Hidden
BINO Alessia
art. 15 (e) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
Hidden