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Classic Retinal Probe Cryo Ii
EUDAMEDClass IIb (EU MDR)
Ref 2509-P-8030
by Keeler Ltd
Identity
- Trade Name
- CLASSIC RETINAL PROBE CRYO II EUDAMED
- Device Name
- CLASSIC RETINAL PROBE CRYO II EUDAMED
- Model / Reference
- 2509-P-8030 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055272718981 EUDAMED
- Basic UDI-DI
- B-05055272718981 EUDAMED
- EMDN Code
- L1705 OPHTHALMOLOGY PROBES, REUSABLE EUDAMED
Classification
- Device Class
- Class IIb EUDAMED
- Market of Registration
- Spain 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
Classic Retinal Probe Cryo Ii by Keeler Ltd — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05055272718981 | Class IIb | Active |
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Manufacturer
- Manufacturer
- Keeler Ltd
- EUDAMED SRN
- GB-MF-000009031
- Authorised Representative
- Keeler Europe Distribution, S.L. ES-AR-000001559
Sources (1)
- EUDAMED a2c50523-0a89-4fde-9323-d93d6cf2fecc 61 fields · synced Jul 12, 2026