Statistics for LINKVERSE S.R.L.

6Total Devices

3Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for LINKVERSE S.R.L.

No certificates registered for this manufacturer.

Showing 1–6 of 6 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
CPRO41S-EU	`CPRO41S-EU`	`08055060110352`	1	On the market
CPRO41-EU	`CPRO41-EU`	`08055060110307`	1	On the market
GGM100	`GGM100`	`08055060110253`	1	On the market
GGM200	`GGM200`	`08055060110260`	1	On the market
GGM300-EU	`GGM300-EU`	`08055060110406`	1	On the market
CB1708-SW3	`CB1708-SW3`	`08055060110239`	1	On the market

Devices placed in 1 country

EUDAMED update: Mar 9, 2026

IT-MF-000029440

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

SEGRETO Alessio
MDR 2017/745, Article 15(3): - Device conformity appropriate check, in accordance with the QMS under which the devices are manufactured, before release; - Technical documentation and EU declaration of conformity are drawn up and kept up-to-date; - Compliance of the post-market surveillance obligations according to Art.10(10); - Fulfilling of reporting obligations referred to in Art. 87 to 91; - For investigational devices, issuing of the statement referred to in Sec. 4.1, of Chp. II of An. XV.
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