← Back to catalogue

9476

EUDAMED

Class IIa (EU MDR)

Ref 9476

by Oy Fluorplast Ab

Identity

Device Name
9476 EUDAMED
Model / Reference
9476 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033408520 EUDAMED
Basic UDI-DI
B-06430033408520 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

Category: Oxygen administration tubing

9476 by Oy Fluorplast Ab — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Oxygen administration tubing.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Oy Fluorplast Ab
EUDAMED SRN
FI-MF-000015708

Sources (1)

  • EUDAMED 3ea96a54-9034-446a-a5d9-452c6ed2f3ca 61 fields · synced Jul 26, 2026