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Suction Tube

EUDAMED

Class I (EU MDR)

Ref 9317

by Oy Fluorplast Ab

Identity

Device Name
Suction Tube EUDAMED
Model / Reference
9317 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033406175 EUDAMED
Basic UDI-DI
B-06430033406175 EUDAMED
EMDN Code
A0399 TUBULAR DEVICES - OTHER EUDAMED

Classification

Device Class
Class I 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

Suction Tube by Oy Fluorplast Ab — Class I — 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 f120ecce-4619-4063-95ad-0f46ce4484df 61 fields · synced Jun 19, 2026