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Halux N50-3 P FX

EUDAMED

Class I (EU MDR)

Ref D16159000

by Derungs Licht AG

Identity

Trade Name
Halux N50-3 P FX EUDAMED
Device Name
Examination light EUDAMED
Model / Reference
D16159000 EUDAMED

Identifiers

Primary DI / UDI-DI
07640158710616 EUDAMED
Basic UDI-DI
76401587118S EUDAMED
EMDN Code
Z129004 LIGHT SOURCES 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

Halux N50-3 P FX by Derungs Licht AG — 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
Derungs Licht AG
EUDAMED SRN
CH-MF-000015827
Authorised Representative
Derungs Medical GmbH DE-AR-000033841

Sources (1)

  • EUDAMED 44639903-934c-48cf-b337-410f29692d2a 61 fields · synced Jun 18, 2026