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Light Guide

EUDAMED

Class I (EU MDR)

Ref UNT-LC3000.35

by Unintech GmbH

Identity

Device Name
Light Guide EUDAMED
Model / Reference
UNT-LC3000.35 EUDAMED

Identifiers

Primary DI / UDI-DI
04262478192472 EUDAMED
Basic UDI-DI
426070601031LGJG EUDAMED
Direct Marketing DI
04262478192472 EUDAMED
EMDN Code
Z12020480 INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - HARDWARE ACCESSORIES 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

Light Guide by Unintech GmbH — 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
Unintech GmbH
EUDAMED SRN
DE-MF-000005136

Sources (1)

  • EUDAMED e9334bc9-7797-4a4f-9c7c-7b69defc039a 61 fields · synced Jun 18, 2026