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Lumorinse

EUDAMED

Class IIa (EU MDR)

Ref N/A

by Koite Health Oy

Identity

Trade Name
Lumorinse EUDAMED
Device Name
Lumorinse EUDAMED
Model / Reference
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06429810197214 EUDAMED
Basic UDI-DI
6429810197Lumorinsetabl4P EUDAMED
EMDN Code
Z12040202 PHOTOTHERAPY EQUIPMENT 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Red-light phototherapy unit, professional

Lumorinse by Koite Health Oy — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Red-light phototherapy unit, professional.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Koite Health Oy
EUDAMED SRN
FI-MF-000006901

Sources (1)

  • EUDAMED d0f0d0c1-7d15-4579-bf73-8c663c790312 61 fields · synced Jun 18, 2026