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2.8v Streak Led Retinoscope & Professional Ophthalmoscope
EUDAMEDFDA UDIClass I (EU MDR)
Ref 1427-P-1101
by Keeler Ltd
Identity
- Trade Name
- 2.8V STREAK LED RETINOSCOPE & PROFESSIONAL OPHTHALMOSCOPE EUDAMED2.8V STREAK LED RET & PROF OPHTH FDA UDI
- Generic Name
- Retinoscope, line-powered FDA UDI
- Device Name
- Ophthalmic/otologic diagnostic set EUDAMED
- Model / Reference
- 1427-P-1101 EUDAMEDFDA UDI
Identifiers
- Primary DI / UDI-DI
- 05055272713047 EUDAMEDFDA UDI
- Basic UDI-DI
- 5055272745084XR EUDAMED
- Direct Marketing DI
- 05055272713047 EUDAMED
- FDA Product Code
- HKL FDA UDI
- EMDN Code
- Z12120199 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER 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
- Portugal 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 Streak Led Retinoscope & Professional Ophthalmoscope 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 | 5055272745084XR | 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 06c87099-86ff-446b-a24a-328076cb3160 61 fields · synced Jun 19, 2026
- FDA UDI eea9a578-243e-4205-a0f3-2bf7abe3ac23 32 fields · synced May 30, 2026