Statistics for SPI

21Total Devices

14Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for SPI

No certificates registered for this manufacturer.

Showing 1–21 of 21 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
CIE01	`CIE01`	`D-CIE01U2`	1	On the market
CNP01	`CNP01`	`D-CNP01WU`	1	On the market
CNP02	`CNP02`	`D-CNP02WW`	1	On the market
CNP03	`CNP03`	`D-CNP03WY`	1	On the market
KG02	`KG02`	`D-KG02J7`	1	On the market
KG03	`KG03`	`D-KG03J9`	1	On the market
KG01	`KG01`	`D-KG01J5`	1	On the market
KN01	`KN01`	`D-KN01K8`	1	On the market
KN02	`KN02`	`D-KN02KA`	1	On the market
KTA-V IT	`KTA-V IT`	`08057157500046`	1	On the market
KT01	`KT01`	`D-KT01L6`	1	On the market
KT03	`KT03`	`D-KT03LA`	1	On the market
KTA-C IT	`KTA-C IT`	`08057157500770`	2	On the market
KTB-V IT	`KTB-V IT`	`08057157500060`	1	On the market
KT02	`KT02`	`D-KT02L8`	1	On the market
KT04	`KT04`	`D-KT04LC`	1	On the market
KTB-C IT	`KTB-C IT`	`08057157500794`	2	On the market
KTA-C ES	`KTA-C ES`	`08057157500787`	2	On the market
KTB-C ES	`KTB-C ES`	`08057157500800`	2	On the market
KTB-V ES	`KTB-V ES`	`08057157500473`	1	On the market
KTA-V ES	`KTA-V ES`	`08057157500466`	1	On the market

Devices placed in 1 country

EUDAMED update: Apr 14, 2026

IT-MF-000029129

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

PANTANO Doriana
ensuring that: - the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; - the post-market surveillance obligations are complied with in accordance with Article 10(10); - in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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D'AMORA Vania
ensuring that: - the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; - the Declarations of Conformity of individual batches of medical devices are correctly drawn up and signed.
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BARALDO Karin
ensuring that: - the reporting obligations referred to in Articles 87 to 91 are fulfilled;
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