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Frami-EyeXplor Module Sinusoïdal

EUDAMED

Class I (EU MDR)

Ref FRAMI-EYEX-SINUModel EYEXPLOR

by Framiral

Identity

Trade Name
Frami-EyeXplor Module Sinusoïdal EUDAMED
Device Name
EYEXPLOR FRAMIRAL EUDAMED
Model / Reference
EYEXPLOR EUDAMED
FRAMI-EYEX-SINU EUDAMED

Identifiers

Primary DI / UDI-DI
03760364680214 EUDAMED
Basic UDI-DI
376036468FRAMI-EYEX3N EUDAMED
EMDN Code
Z12140401 VESTIBULAR ASSESSMENT SYSTEMS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Frami-EyeXplor Module Sinusoïdal by Framiral — 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

Manufacturer
Framiral
EUDAMED SRN
FR-MF-000011744

Sources (1)

  • EUDAMED 9e7b1c51-e88d-4343-a36b-51f66a73baaa 61 fields · synced Jul 21, 2026