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GlassOuse Assistive Device

EUDAMED

Class I (EU MDR)

Ref GlassOusePROModel GlassOuse PRORef GlassOuse V1.4

by EnnoPro Group Limited

Identity

Trade Name
GlassOuse Assistive Device EUDAMED
Device Name
GlassOuse Assistive Device EUDAMED
Model / Reference
GlassOuse PRO EUDAMED
GlassOusePRO EUDAMED
GlassOuse V1.4 EUDAMED

Identifiers

Primary DI / UDI-DI
06978224010003 EUDAMED
06978224010027 EUDAMED
Basic UDI-DI
697822401GlassOusePROA9 EUDAMED
697822401GlassOuseV1.44K EUDAMED
EMDN Code
Y241203 PROGRAMMABLE REMOTE CONTROLS, HOME AUTOMATION SYSTEMS, CONTROL SATELLITES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

GlassOuse Assistive Device by EnnoPro Group Limited — 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-000047550
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (2)

  • EUDAMED a983d35a-63a2-47bd-b1b9-50e7d24b637f 61 fields · synced Jul 27, 2026
  • EUDAMED d445d668-1151-4caf-a3f7-5c977a76dcd8 61 fields · synced May 18, 2026