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2.8v Professional Spot Retinoscope In Case
EUDAMEDFDA UDIClass I (EU MDR)
Ref 1302-P-1008
by Keeler Ltd
Identity
- Trade Name
- 2.8V PROFESSIONAL SPOT RETINOSCOPE IN CASE EUDAMED2.8V PROFESSIONAL SPOT RET & CASE FDA UDI
- Generic Name
- Retinoscope, line-powered FDA UDI
- Device Name
- Retinoscope EUDAMED
- Model / Reference
- 1302-P-1008 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055272701570 EUDAMEDFDA UDI
- Basic UDI-DI
- 50552727RETINOSCOPESD7 EUDAMED
- Direct Marketing DI
- 05055272701570 EUDAMED
- FDA Product Code
- HKL FDA UDI
- EMDN Code
- Z12120118 RETINOSCOPES EUDAMED
- GMDN Term
- Retinoscope, line-powered FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 886.1780 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
2.8v Professional Spot Retinoscope In Case by Keeler Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 50552727RETINOSCOPESD7 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Keeler Ltd
- EUDAMED SRN
- GB-MF-000009031
- Authorised Representative
- Keeler Europe Distribution, S.L. ES-AR-000001559
Sources (2)
- EUDAMED b733fdc1-8d6f-4de8-829e-f986b7c4c897 61 fields · synced Jul 26, 2026
- FDA UDI a5bf973f-3820-4c62-9670-3a87f26b03ff 32 fields · synced May 25, 2026