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9781

EUDAMED

Class IIa (EU MDR)

Ref 9781

by Oy Fluorplast Ab

Identity

Device Name
9781 EUDAMED
Model / Reference
9781 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033404508 EUDAMED
Basic UDI-DI
B-06430033404508 EUDAMED
EMDN Code
R03010204 OXYGEN ADMINISTRATION TUBINGS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland 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

9781 by Oy Fluorplast Ab — Class IIa — 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
Oy Fluorplast Ab
EUDAMED SRN
FI-MF-000015708

Sources (1)

  • EUDAMED 2e625830-a8eb-4de8-9b3b-95feff4f7923 61 fields · synced Jul 16, 2026