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 1–25 of 63 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
ADMR101.10	`ADMR101.10`	`08056304411341`	6	On the market
246009	`246009`	`08056304411822`	12	On the market
246008	`246008`	`08056304411808`	12	On the market
246007	`246007`	`08056304411785`	12	On the market
246006	`246006`	`08056304411761`	12	On the market
ADMR204.100	`ADMR204.100`	`08056304411402`	12	On the market
ADBP03	`ADBP03`	`08056304410207`	2	On the market
AD001WD/L	`AD001WD/L`	`08056304410047`	2	On the market
AD002WD	`AD002WD`	`08056304410054`	1	On the market
AD003WD	`AD003WD`	`08056304410061`	1	On the market
AD001WD/L	`AD001WD/L`	`08056304410009`	1	On the market
AD004WD	`AD004WD`	`08056304410078`	1	On the market
ADWD300.51	`ADWD300.51`	`08056304411174`	2	On the market
ADWD300.250	`ADWD300.250`	`08056304411198`	1	On the market
ADWD300.100	`ADWD300.100`	`08056304411181`	1	On the market
ADWD300.50	`ADWD300.50`	`08056304411150`	2	On the market
ADWD03	`ADWD03`	`08056304410306`	2	On the market
ADMR09	`ADMR09`	`08056304410665`	12	On the market
ADMR103.50	`ADMR103.50`	`08056304411525`	4	On the market
ADMR103.075	`ADMR103.075`	`08056304411327`	12	On the market
ADMR100.50	`ADMR100.50`	`08056304411112`	4	On the market
ADMR100.10	`ADMR100.10`	`08056304411099`	12	On the market
AD009WD	`AD009WD`	`08056304410023`	2	On the market
AD009WDL	`AD009WDL`	`08056304410122`	2	On the market
AD010WD	`AD010WD`	`08056304410139`	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