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Visiotest

EUDAMED

Class I (EU MDR)

Ref C77301

by Essilor International

Identity

Trade Name
VISIOTEST EUDAMED
Device Name
VISIOTEST EUDAMED
Model / Reference
C77301 EUDAMED

Identifiers

Primary DI / UDI-DI
03615020000618 EUDAMED
Basic UDI-DI
361502000000IVISIOTEST0WJ EUDAMED
EMDN Code
Z1212012099 INSTRUMENTS FOR THE ASSESSMENT OF VISUAL FUNCTIONALITY - OTHER 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

Visiotest by Essilor International — 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
FR-MF-000007175

Sources (1)

  • EUDAMED 97daebb8-e4a4-4a99-bfa8-a900717b513f 61 fields · synced Jun 19, 2026