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OculoSpect

EUDAMED

Class I (EU MDR)

Ref 669-302022

by Opticus Doo Belgrade

Identity

Device Name
OculoSpect EUDAMED
Model / Reference
669-302022 EUDAMED

Identifiers

Primary DI / UDI-DI
08605044403590 EUDAMED
Basic UDI-DI
86050444OculoSpectSN EUDAMED
EMDN Code
Q0210010103 PROGRESSIVE ORGANIC OPHTHALMIC LENSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Croatia 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

OculoSpect by Opticus Doo Belgrade — 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
RS-MF-000041064
Authorised Representative
Salus Cons Kft. HU-AR-000006177

Sources (1)

  • EUDAMED 7a6eccdd-8aa3-414e-881e-41c46c7f7c57 61 fields · synced Jun 19, 2026