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Ophthalmic Retractor
EUDAMEDClass I (EU MDR)
Ref R-021Model Ophthalmic Retractor
by CILITA Ltd.
Identity
- Device Name
- Ophthalmic Retractor EUDAMED
- Model / Reference
- Ophthalmic Retractor EUDAMEDR-021 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04610274509084 EUDAMED
- Basic UDI-DI
- 468017344CILORAY EUDAMED
- EMDN Code
- L170102 OCULAR AND ENDOCULAR RETRACTORS, 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 Retractor 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 468017344CILORAY | 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 a3e71740-37a5-48f0-b6a2-83cf6bf52ba8 61 fields · synced Jun 19, 2026