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Stimulopt

EUDAMED

Class I (EU MDR)

Ref STIMUL-EUModel Boule Optocinétique Stimulopt Framiral

by Framiral

Identity

Trade Name
STIMULOPT EUDAMED
Device Name
STIMULOPT EUDAMED
Model / Reference
Boule Optocinétique Stimulopt Framiral EUDAMED
STIMUL-EU EUDAMED

Identifiers

Primary DI / UDI-DI
03760364680009 EUDAMED
Basic UDI-DI
376036468STIMUL-EU3U EUDAMED
EMDN Code
Z129013 GENERAL AUDITORY AND/OR VISUAL STIMULATORS 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

Category: Auditory stimulator

Stimulopt by Framiral — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Auditory stimulator.

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 b134cbfc-91f5-427c-8a74-180505c88d5c 61 fields · synced Jun 19, 2026