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9362

EUDAMED

Class IIa (EU MDR)

Ref 9362

by Oy Fluorplast Ab

Identity

Device Name
9362 EUDAMED
Model / Reference
9362 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033406625 EUDAMED
Basic UDI-DI
B-06430033406625 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

9362 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 4eeeefc9-e8c7-4da5-b102-5f8bfa2b3c3d 61 fields · synced Jul 27, 2026