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Ophthalmic curette
EUDAMEDClass I (EU MDR)
Ref M-040Model Ophthalmic curette
by CILITA Ltd.
Identity
- Device Name
- Ophthalmic curette EUDAMED
- Model / Reference
- Ophthalmic curette EUDAMEDM-040 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04610274508407 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
Category: Ophthalmic curette, reusable
Ophthalmic curette by CILITA Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Ophthalmic curette, reusable.
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 468017344CILOCA2 | Class I | Active |
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Manufacturer
- Manufacturer
- CILITA Ltd.
- EUDAMED SRN
- RU-MF-000041168
- Authorised Representative
- Arazy Group GmbH DE-AR-000007685
Sources (1)
- EUDAMED a5fd6339-cc56-45af-8d78-38a55e9952a7 61 fields · synced Jun 18, 2026