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iLumin

EUDAMED

Class I (EU MDR)

Ref FI-100

by Nova Eye, Inc.

Identity

Trade Name
iLumin EUDAMED
Device Name
Fiberoptic Illuminator EUDAMED
Model / Reference
FI-100 EUDAMED

Identifiers

Primary DI / UDI-DI
00893872001370 EUDAMED
Basic UDI-DI
0893872001Fi-10054 EUDAMED
Direct Marketing DI
00893872001370 EUDAMED
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal 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

iLumin by Nova Eye, Inc. — 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
Nova Eye, Inc.
EUDAMED SRN
US-MF-000011341
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 0fd95911-971f-494e-8a82-9585c0428c1e 61 fields · synced Jun 19, 2026