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Ophthalmic curette

EUDAMED

Class I (EU MDR)

Ref M-041Model Ophthalmic curette

by CILITA Ltd.

Identity

Device Name
Ophthalmic curette EUDAMED
Model / Reference
Ophthalmic curette EUDAMED
M-041 EUDAMED

Identifiers

Primary DI / UDI-DI
04610274508414 EUDAMED
Basic UDI-DI
468017344CILOCA2 EUDAMED
EMDN Code
L1703 OPHTHALMOLOGY CURETTES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Ophthalmic curette by CILITA Ltd. — 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
CILITA Ltd.
EUDAMED SRN
RU-MF-000041168
Authorised Representative
Arazy Group GmbH DE-AR-000007685

Sources (1)

  • EUDAMED 64ef3736-b3e5-4b8c-a86e-5442249b7023 61 fields · synced Jun 18, 2026