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MediLight

EUDAMED

Class IIb (EU MDR)

Ref 666331.0-S13Model K666-Serie

by VTI Ventil Technik GmbH

Identity

Trade Name
MediLight EUDAMED
Device Name
MediLight EUDAMED
Model / Reference
K666-Serie EUDAMED
666331.0-S13 EUDAMED

Identifiers

Primary DI / UDI-DI
04066206400132 EUDAMED
Basic UDI-DI
4066206400005Q EUDAMED
Direct Marketing DI
04066206400132 EUDAMED
EMDN Code
R9080 RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIb 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

Category: Gas-sampling/monitoring respiratory tubing, single-use

MediLight by VTI Ventil Technik GmbH — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gas-sampling/monitoring respiratory tubing, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000006534

Sources (1)

  • EUDAMED 48f74dd0-e5bc-4abe-aafa-9f87915efe44 61 fields · synced Jun 14, 2026