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9302

EUDAMED

Class I (EU MDR)

Ref 9302

by Oy Fluorplast Ab

Identity

Device Name
9302 EUDAMED
Model / Reference
9302 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033406021 EUDAMED
Basic UDI-DI
B-06430033406021 EUDAMED
EMDN Code
A060102 SURGICAL DRAINAGE CONNECTION MEDICAL TUBES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

Yes

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: Suction/irrigation tubing, single-use

9302 by Oy Fluorplast Ab — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

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 7c12bb6b-d16d-4564-87bd-e8f41ccec72b 61 fields · synced Jun 19, 2026