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Luminox

EUDAMED

Class I (EU MDR)

Ref LF90188/LSSDI000BModel Celesta & Luminox

by Eclipse Prism Medical Devices Private Limited

Identity

Trade Name
Luminox EUDAMED
Device Name
Celesta & Luminox EUDAMED
Model / Reference
Celesta & Luminox EUDAMED
LF90188/LSSDI000B EUDAMED

Identifiers

Primary DI / UDI-DI
08906164080181 EUDAMED
Basic UDI-DI
890616408OTLRF EUDAMED
EMDN Code
Z12010701 FIXED SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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: Operating room light system

Luminox by Eclipse Prism Medical Devices Private Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Operating room light system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000032926
Authorised Representative
Mars Medical DE-AR-000006312

Sources (1)

  • EUDAMED e48262b2-0983-4148-b18b-fdc3b6381f92 61 fields · synced Jun 19, 2026