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Bella Lumax

EUDAMED

Class I (EU MDR)

Ref LED22650

by Lid - Sotramet

Identity

Trade Name
BELLA LUMAX EUDAMED
Device Name
BELLA LUMAX EUDAMED
Model / Reference
LED22650 EUDAMED

Identifiers

Primary DI / UDI-DI
03760361831329 EUDAMED
Basic UDI-DI
376036183LUMAXF6 EUDAMED
EMDN Code
Z12010702 MOBILE SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Bella Lumax by Lid - Sotramet — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Lid - Sotramet
EUDAMED SRN
FR-MF-000014659

Sources (1)

  • EUDAMED f8dd2af8-d72a-479d-8691-399e4185ab60 61 fields · synced Jun 19, 2026