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OneWound

EUDAMED

Class I (EU MDR)

Ref 2000020

by OneMed Group Oy

Identity

Trade Name
OneWound EUDAMED
Device Name
OneWound EUDAMED
Model / Reference
2000020 EUDAMED

Identifiers

Primary DI / UDI-DI
D-2000020SU EUDAMED
Basic UDI-DI
B-2000020SU EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Special Device Type
-1192 EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

OneWound by OneMed Group Oy — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
OneMed Group Oy
EUDAMED SRN
FI-MF-000000642

Sources (1)

  • EUDAMED 58cb24ed-1c2f-4a40-bd38-b71430fc51c3 61 fields · synced Jun 18, 2026