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9405

EUDAMED

Class IIa (EU MDR)

Ref 9405

by Oy Fluorplast Ab

Identity

Device Name
9405 EUDAMED
Model / Reference
9405 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033400258 EUDAMED
Basic UDI-DI
B-06430033400258 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

9405 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 88fc2d66-ee2d-4fb4-a2dd-34962f4c30bb 61 fields · synced Jun 18, 2026