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Sil030060

EUDAMED

Class I (EU MDR)

Ref SIL030060

by Oy Fluorplast Ab

Identity

Device Name
SIL030060 EUDAMED
Model / Reference
SIL030060 EUDAMED

Identifiers

Primary DI / UDI-DI
06430033400920 EUDAMED
Basic UDI-DI
B-06430033400920 EUDAMED
EMDN Code
A03020101 LOW PRESSURE EXTENSION LINES 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

Sil030060 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 33b885f3-101b-4b9e-a29d-2c02e83da00e 61 fields · synced Jun 19, 2026