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ARC 514/810nm

EUDAMED

Class IIb (EU MDR)

Ref 1205-P-2070

by Keeler Ltd

Identity

Trade Name
ARC 514/810nm EUDAMED
Device Name
Laser Indirect Ophthalmoscope EUDAMED
Model / Reference
1205-P-2070 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272712798 EUDAMED
Basic UDI-DI
B-05055272712798 EUDAMED
EMDN Code
Z12120199 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

ARC 514/810nm by Keeler Ltd — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Keeler Ltd
EUDAMED SRN
GB-MF-000009031
Authorised Representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Sources (1)

  • EUDAMED 94f7d818-cd6d-4fe7-bc01-3df41caac648 61 fields · synced Jun 18, 2026