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9370

EUDAMED

Class IIa (EU MDR)

Ref 9370

by Oy Fluorplast Ab

Identity

Device Name
9370 EUDAMED
Model / Reference
9370 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033406700 EUDAMED
Basic UDI-DI
B-06430033406700 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

9370 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

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Manufacturer

Manufacturer
Oy Fluorplast Ab
EUDAMED SRN
FI-MF-000015708

Sources (1)

  • EUDAMED ccf2d595-34b4-4751-a0ed-22f48990942b 61 fields · synced Jun 18, 2026