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Ophthalmic forceps
EUDAMEDClass I (EU MDR)
Ref F-0811TModel Ophthalmic forceps
by CILITA Ltd.
Identity
- Device Name
- Ophthalmic forceps EUDAMED
- Model / Reference
- Ophthalmic forceps EUDAMEDF-0811T EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04610274505673 EUDAMED
- Basic UDI-DI
- 468017344CILOFA8 EUDAMED
- EMDN Code
- L170201 OPHTHALMIC GRASPING FORCEPS, 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 forceps 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 | 468017344CILOFA8 | 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 7c0ea9f5-b58d-4dec-b5c3-2423206296b3 61 fields · synced Jun 19, 2026