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VISIANO 20-2 Pro P TX

EUDAMED

Class I (EU MDR)

Ref D16378000Ref D16379000

by Derungs Licht AG

Identity

Trade Name
VISIANO 20-2 Pro P TX EUDAMED
Device Name
Examination light EUDAMED
Model / Reference
D16378000 EUDAMED
D16379000 EUDAMED

Identifiers

Primary DI / UDI-DI
07640158713198 EUDAMED
07640158713136 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

VISIANO 20-2 Pro P TX 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 (2)

  • EUDAMED cdc567cb-32a8-44fc-be51-64f5c9eaf559 61 fields · synced Jul 29, 2026
  • EUDAMED 72b7ba6c-6453-47da-9119-c74e3295f63e 61 fields · synced May 18, 2026