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Neo-Vista

EUDAMED

Class I (EU MDR)

Ref TRANS1Model Neo-Vista

by Conlett Technology Inc

Identity

Trade Name
Neo-Vista EUDAMED
Device Name
Neo-Vista EUDAMED
Model / Reference
Neo-Vista EUDAMED
TRANS1 EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010507 EUDAMED
Basic UDI-DI
697359601Neo-VistaCJ EUDAMED
Direct Marketing DI
06973596010507 EUDAMED
EMDN Code
W0202030202 TRANSILLUMINATORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Neo-Vista by Conlett Technology Inc — 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

EUDAMED SRN
CN-MF-000002101
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 78bf3aa2-91bb-4213-89e1-87303d55547f 61 fields · synced Jul 10, 2026