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HOIVA Antiseptinen Suihke

EUDAMED

Class IIa (EU MDR)

Ref TK403

by Fysioline Oy

Identity

Trade Name
HOIVA Antiseptinen Suihke EUDAMED
Device Name
HOIVA Antiseptinen Suihke EUDAMED
Model / Reference
TK403 EUDAMED

Identifiers

Primary DI / UDI-DI
D-6430029912451VS EUDAMED
Basic UDI-DI
B-6430029912451VS EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

Yes

EUDAMED

HOIVA Antiseptinen Suihke by Fysioline Oy — 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
Fysioline Oy
EUDAMED SRN
FI-MF-000001173

Sources (1)

  • EUDAMED 576cb765-479d-47b8-aa7d-fe9130b922f9 61 fields · synced Jul 10, 2026