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Smartlax peräruiske 12x5ml

EUDAMED

Class I (EU MDR)

Ref 2150159

by Galena Pharma Oy

Identity

Trade Name
Smartlax peräruiske 12x5ml EUDAMED
Device Name
Smartlax peräruiske EUDAMED
Model / Reference
2150159 EUDAMED

Identifiers

Primary DI / UDI-DI
06417927103402 EUDAMED
Basic UDI-DI
B-06417927103402 EUDAMED
EMDN Code
G99 GASTROINTESTINAL DEVICES - OTHER 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

Smartlax peräruiske 12x5ml by Galena Pharma Oy — 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
Galena Pharma Oy
EUDAMED SRN
FI-MF-000000588

Sources (1)

  • EUDAMED 4754b09b-1f9b-4967-b59a-12a76bdec5ab 61 fields · synced Jul 16, 2026