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Innokas Yhtymä Oy

Inactive in EUDAMED since 2025

Finlandfrom SRN EUDAMED FDA SRN FI-MF-000005374

Inactive. This company's EUDAMED actor record is marked inactive. Check the current status before ordering.

Devices
1
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA establishment

What Innokas Yhtymä Oy makes

Innokas Yhtymä Oy manufactures the CARESCAPE VC150, a vital signs monitor designed to measure and display physiological parameters such as heart rate, blood pressure, and oxygen saturation for patient monitoring in clinical settings.

The company’s devices fall under EU Class IIb classification and are listed in the eudamed registry. Innokas Yhtymä Oy operates from Finland.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • CARESCAPE VC150 Vital Signs Monitor Ref 2067980

    Active Regimes: 510(k) CE MDD, withdrawn Registry: EUDAMEDGUDID Class:IIb

Company details

EUDAMED SRN
FI-MF-000005374
EU VAT number
FI21856799
EUDAMED status
Inactive since 2025
EUDAMED registered name
Innokas Yhtymä Oy
Registered address
10, Vihikari, 90440, Kempele, Finland
Phone
+358 8 562 3100
PRRC contact
Päivi Isomaki(public in EUDAMED)

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Innokas Yhtymä Oy US

From the company website

Read 18 Oct 2026

Trusted Nordic partner for contract design, development, manufacturing, and QA/RA services for smart electromechanical devices and high‑tech industries.

From the manufacturer's own website. Source

Frequently asked questions

How many devices does Innokas Yhtymä Oy have in the registry?

The registry currently lists 1 device for Innokas Yhtymä Oy. Devices recorded under merged duplicate company entries are counted once.

Which registries list Innokas Yhtymä Oy's devices?

Among its 1 most recently registered device, Innokas Yhtymä Oy has devices listed in EUDAMED (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Innokas Yhtymä Oy's devices fall under?

Among its 1 most recently registered device, the classes recorded for Innokas Yhtymä Oy's devices are Class IIb. Each device page shows its own class and authorisation.

What are the newest devices from Innokas Yhtymä Oy in the registry?

The most recently registered devices listed for Innokas Yhtymä Oy include CARESCAPE VC150 Vital Signs Monitor.

Which FDA establishments are linked to Innokas Yhtymä Oy?

1 FDA establishment is linked to Innokas Yhtymä Oy in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.