← Back to catalogue

Amalia 2 B S8

EUDAMED

Class I (EU MDR)

Ref D16373000Ref D16371000

by Derungs Licht AG

Identity

Trade Name
AMALIA 2 B S8 EUDAMED
Device Name
Examination light EUDAMED
Model / Reference
D16373000 EUDAMED
D16371000 EUDAMED

Identifiers

Primary DI / UDI-DI
07640158713082 EUDAMED
07640158713068 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

Amalia 2 B S8 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Derungs Licht AG
EUDAMED SRN
CH-MF-000015827
Authorised Representative
Derungs Medical GmbH DE-AR-000033841

Sources (2)

  • EUDAMED c7ae2a50-5038-45cf-b445-7d6dc2eb8f6e 61 fields · synced Jul 30, 2026
  • EUDAMED 1a82e3bd-87d2-40b8-8a24-c2594a40e140 61 fields · synced May 18, 2026