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VISUSTAR go

EUDAMED

Class I (EU MDR)

Ref 000000-2542-400

by Carl Zeiss Vision GmbH

Identity

Trade Name
VISUSTAR go EUDAMED
Device Name
VISUSTAR go EUDAMED
Model / Reference
000000-2542-400 EUDAMED

Identifiers

Primary DI / UDI-DI
04250668607196 EUDAMED
Basic UDI-DI
42506686-S01-VSGO-G3 EUDAMED
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Special Device Type
Software 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

VISUSTAR go by Carl Zeiss Vision 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

EUDAMED SRN
DE-MF-000006173

Sources (1)

  • EUDAMED a61547be-83d6-455c-9280-514b7a6187c2 61 fields · synced Jul 13, 2026