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9250

EUDAMED

Class IIa (EU MDR)

Ref 9250

by Oy Fluorplast Ab

Identity

Device Name
9250 EUDAMED
Model / Reference
9250 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033401507 EUDAMED
Basic UDI-DI
B-06430033401507 EUDAMED
EMDN Code
A06010199 VACUUM AND GRAVITY DRAINAGE SYSTEMS - OTHER EUDAMED

Classification

Device Class
Class IIa 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

9250 by Oy Fluorplast Ab — Class IIa — 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 aed613c1-a847-4f18-b33c-35fffcc9da4a 61 fields · synced Jul 9, 2026