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Fingerdual

EUDAMED

Class I (EU MDR)

Ref FD30

by Berner Oy

Identity

Trade Name
Fingerdual EUDAMED
Device Name
Pikobutton EUDAMED
Model / Reference
FD30 EUDAMED

Identifiers

Primary DI / UDI-DI
06414505180770 EUDAMED
Basic UDI-DI
6414505PBS3 EUDAMED
Direct Marketing DI
06414505180770 EUDAMED
EMDN Code
Y2199 COMMUNICATION AND INFORMATION MANAGEMENT AIDS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Fingerdual by Berner Oy — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Berner Oy
EUDAMED SRN
FI-MF-000007402

Sources (1)

  • EUDAMED 12fea839-eaec-4d4e-9157-562e46859664 61 fields · synced Jun 18, 2026