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 26–50 of 63 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
AD010WD	`AD010WD`	`08056304410139`	1	On the market
AD012WD	`AD012WD`	`08056304410153`	1	On the market
ADMR06	`ADMR06`	`08056304410252`	12	On the market
AD005WD	`AD005WD`	`08056304410016`	2	On the market
AD008WD	`AD008WD`	`08056304410115`	1	On the market
AD005WDL	`AD005WDL`	`08056304410085`	2	On the market
AD006WD	`AD006WD`	`08056304410092`	1	On the market
AD007WD	`AD007WD`	`08056304410108`	1	On the market
ADMR102.50	`ADMR102.50`	`08056304411396`	4	On the market
ADMR102.10	`ADMR102.10`	`08056304411372`	12	On the market
ADMR101.20	`ADMR101.20`	`08056304411365`	4	On the market
AD005MR	`AD005MR`	`08056304410030`	2	On the market
AD002MR	`AD002MR`	`08056304410177`	12	On the market
AD004MR	`AD004MR`	`08056304410191`	4	On the market
AD001MR	`AD001MR`	`08056304410160`	12	On the market
AD003MR	`AD003MR`	`08056304410184`	6	On the market
ADMR201.50	`ADMR201.50`	`08056304411235`	4	On the market
ADMR201.10	`ADMR201.10`	`08056304411228`	12	On the market
ADMR201.075	`ADMR201.075`	`08056304411204`	12	On the market
ADBP04	`ADBP04`	`08056304410221`	2	On the market
ADMR202.10	`ADMR202.10`	`08056304411266`	12	On the market
ADMR202.075	`ADMR202.075`	`08056304411242`	12	On the market
ADMR202.50	`ADMR202.50`	`08056304411273`	4	On the market
ADMR11	`ADMR11`	`08056304410733`	12	On the market
ADMR200.10	`ADMR200.10`	`08056304411129`	12	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