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9288

EUDAMED

Class IIa (EU MDR)

Ref 9288

by Oy Fluorplast Ab

Identity

Device Name
9288 EUDAMED
Model / Reference
9288 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033401880 EUDAMED
Basic UDI-DI
B-06430033401880 EUDAMED
EMDN Code
A06010103 CANNULAS AND TIPS FOR ASPIRATION AND IRRIGATION, SINGLE-USE 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

9288 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 c0655ed8-9451-4835-ad1c-c2eee93eea6b 61 fields · synced Jun 18, 2026