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Vista Plus

EUDAMED

Class I (EU MDR)

Ref TRANS2Model Vista Plus

by Conlett Technology Inc

Identity

Trade Name
Vista Plus EUDAMED
Device Name
Vista Plus EUDAMED
Model / Reference
Vista Plus EUDAMED
TRANS2 EUDAMED

Identifiers

Primary DI / UDI-DI
06973596010200 EUDAMED
Basic UDI-DI
697359601VistaPlusF4 EUDAMED
Direct Marketing DI
06973596010200 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

Vista Plus 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 5666e01f-768e-470e-9900-7426e6734294 61 fields · synced Aug 2, 2026