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Celesta

EUDAMED

Class I (EU MDR)

Ref LF90025/CSDDFF000Model Celesta & Luminox

by Eclipse Prism Medical Devices Private Limited

Identity

Trade Name
Celesta EUDAMED
Device Name
Celesta & Luminox EUDAMED
Model / Reference
Celesta & Luminox EUDAMED
LF90025/CSDDFF000 EUDAMED

Identifiers

Primary DI / UDI-DI
08906164080266 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

Celesta 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 cc7d53f1-c34d-4e56-8b9e-a10bdaeeddf4 61 fields · synced Jun 19, 2026