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RetinAI Discovery

EUDAMED

Class IIa (EU MDR)

Ref 07640486840856

by Ikerian AG

Identity

Device Name
RetinAI Discovery EUDAMED
Model / Reference
07640486840856 EUDAMED

Identifiers

Primary DI / UDI-DI
07640486840856 EUDAMED
Basic UDI-DI
764048684Discovery18091G4 EUDAMED
EMDN Code
Z12120192 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS - MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

RetinAI Discovery by Ikerian AG — Class IIa — 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
Ikerian AG
EUDAMED SRN
CH-MF-000014537
Authorised Representative
Blue Broccoli GmbH LI-AR-000000233

Sources (1)

  • EUDAMED e466e4d2-5e59-45dc-bdcf-0be3a914f17b 61 fields · synced Jun 18, 2026