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Veinlite LEDX

EUDAMED

Class I (EU MDR)

Ref VLEDX

by Translite, LLC

Identity

Trade Name
Veinlite LEDX EUDAMED
Device Name
Veinlite LEDX EUDAMED
Model / Reference
VLEDX EUDAMED

Identifiers

Primary DI / UDI-DI
00195893754281 EUDAMED
Basic UDI-DI
B-00195893754281 EUDAMED
EMDN Code
W0202030202 TRANSILLUMINATORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Veinlite LEDX by Translite, LLC — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Translite, LLC
EUDAMED SRN
US-MF-000029360
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (1)

  • EUDAMED c75c687f-db52-4e0c-8ff2-e4b9e4669ba9 61 fields · synced Jul 21, 2026