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Pikodual 50 75g

EUDAMED

Class I (EU MDR)

Ref PD50H

by Berner Oy

Identity

Trade Name
Pikodual 50 75g EUDAMED
Device Name
Pikobutton EUDAMED
Model / Reference
PD50H EUDAMED

Identifiers

Primary DI / UDI-DI
06414505180572 EUDAMED
Basic UDI-DI
6414505PBS3 EUDAMED
Direct Marketing DI
06414505180572 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

Pikodual 50 75g 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 e0082800-e4fd-4da3-8a68-eed6ca93f023 61 fields · synced Jun 18, 2026