Statistics for Mesa

238Total Devices

4Basic UDI-DIs

0Not destined for EU market

1Certificates

1Valid

0Expiring < 6 months

1Countries

Certificate health for Mesa

Showing 226–238 of 238 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
40080015A	`40080015A`	`08050612204381`	1	On the market
40080018A	`40080018A`	`08050612204398`	1	On the market
40080006A	`40080006A`	`08050612204374`	1	On the market
40080002A	`40080002A`	`08050612204367`	1	On the market
40090029A	`40090029A`	`08050612204442`	1	On the market
40090038A	`40090038A`	`08050612204466`	1	On the market
40090017A	`40090017A`	`08050612204435`	1	On the market
40090025A	`40090025A`	`08050612201229`	1	On the market
40090001A	`40090001A`	`08050612201199`	1	On the market
40090033A	`40090033A`	`08050612204473`	1	On the market
40090030A	`40090030A`	`08050612204459`	1	On the market
40090027A	`40090027A`	`08050612200192`	1	On the market
40090028A	`40090028A`	`08050612204428`	1	On the market

Devices placed in 1 country

EUDAMED update: May 11, 2026

IT-MF-000029407

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

SALA Lorenzo
Check the compliance of the devices according to the QMS under which the devices are manufactured before release. Draw up and update the technical documentation and the EU declaration of conformity. Management of PMS obligations. Management of reporting obligations. In the case of devices under investigation, issue the declaration referred to in Annex XV, Chapter II, point 4.1 of the MDR.
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