Statistics for Icare Finland Oy

26Total Devices

17Basic UDI-DIs

0Not destined for EU market

2Certificates

2Valid

0Expiring < 6 months

1Countries

Certificate health for Icare Finland Oy

Showing 26–26 of 26 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Ventica Shirt, 80-90 cm	`VE130`	`06430033850824`	1	On the market

Devices placed in 1 country

EUDAMED update: Mar 7, 2025

FI-MF-000000501

Active

Name: Finnish Medicines Agency, Supervision and licences, Medical Device Unit
SRN: FI-CA-006
Phone: +358 29 522 3341
Email: registry@fimea.fi

HYVÖNEN Hannes
-the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date -the reporting obligations referred to in Articles 87 to 91 -in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV
Hidden
HAULISTO Rami
-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 post-market surveillance obligations are complied with in accordance with Article 10(10)
Hidden