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9553a

EUDAMED

Class I (EU MDR)

Ref 9553A

by Oy Fluorplast Ab

Identity

Device Name
9553A EUDAMED
Model / Reference
9553A EUDAMED

Identifiers

Primary DI / UDI-DI
06430033408094 EUDAMED
Basic UDI-DI
B-06430033408094 EUDAMED
EMDN Code
T030199 COVERS, INSTRUMENTS AND EQUIPMENT - OTHER 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

9553a 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 bef7d118-ffa2-4d91-b3a6-a6a42d20a4b6 61 fields · synced Jun 20, 2026