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Megin Oy

Active in EUDAMED

Finlandfrom SRN EUDAMED FDA SRN FI-MF-000011965 FEI 3006563303

Megin Oy is a medical device manufacturer based in Finland, with 36 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II; EU Class IIa) as of 13 Nov 2026.

Devices
36
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 34
  • EUDAMED 6
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 30
  • EU Class IIa 6
Identifiers
  • EUDAMED SRN FI-MF-000011965
  • FDA FEI 3006563303
  • DUNS 538025107

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What Megin Oy makes

Megin Oy manufactures electroencephalographs and magnetoencephalography systems, including devices such as the MEGreview™, various EEG caps with different channel configurations, finger response systems, and patient comfort accessories.

The company's portfolio includes Class II and Class IIa devices listed in eudamed, fda_510k, and fda_udi registries, and is based in Finland.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue36

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Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
FI-MF-000011965
FDA FEI number
3006563303
DUNS number
538025107
EU VAT number
FI07562567
EUDAMED status
Active
EUDAMED registered name
Megin Oy
Registered address
5, Keilasatama, 02150, Espoo, Finland
Website
megin.fi/
Phone
+358 9 756 2400
PRRC contact
Juha Viirola(public in EUDAMED)

Frequently asked questions

How many devices does Megin Oy have in the registry?

The registry currently lists 36 devices for Megin Oy. Devices recorded under merged duplicate company entries are counted once.

Which registries list Megin Oy's devices?

Among its 36 most recently registered devices, Megin Oy has devices listed in EUDAMED (6 devices), FDA 510(k) (1 device) and FDA GUDID (34 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Megin Oy's devices fall under?

Among its 36 most recently registered devices, the classes recorded for Megin Oy's devices are Class IIa and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Megin Oy in the registry?

The most recently registered devices listed for Megin Oy include MEGreview™ SW26241N, Bilateral finger response system NM20999N, Auditory stimulator earphones (VectorView) EL21103J and Child insert for chair BC20899N.

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