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.

Showing 51–63 of 63 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
ADMR200.50	`ADMR200.50`	`08056304411143`	4	On the market
ADMR203.075	`ADMR203.075`	`08056304411280`	12	On the market
ADMR203.10	`ADMR203.10`	`08056304411303`	12	On the market
ADMR203.50	`ADMR203.50`	`08056304411310`	4	On the market
ADMR12	`ADMR12`	`08056304410771`	4	On the market
ADMR13	`ADMR13`	`08056304410788`	12	On the market
ADWD0145	`ADWD0145`	`08056304410276`	1	On the market
ADMR14BT	`ADMR14BT`	`08056304410825`	1	On the market
ADMR14-S	`ADMR14-S`	`08056304410818`	1	On the market
ADMR14WT	`ADMR14WT`	`08056304410832`	1	On the market
249005	`249005`	`08056304410849`	2	On the market
249006	`249006`	`08056304410863`	2	On the market
ADMR08132	`ADMR08132`	`08056304410658`	1	On the market

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