Identity
- Trade Name
- 2.8V STREAK MAGNETIC RET EUDAMED
- Device Name
- Retinoscope EUDAMED
- Model / Reference
- 1302-P-1006 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055272701556 EUDAMED
- Basic UDI-DI
- 50552727RETINOSCOPESD7 EUDAMED
- Direct Marketing DI
- 05055272701556 EUDAMED
- EMDN Code
- Z12120118 RETINOSCOPES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Latvia 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
2.8v Streak Magnetic Ret by Keeler 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 | 50552727RETINOSCOPESD7 | Class I | 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 f7a9d083-4689-47f7-80b1-5bfc41a9c550 61 fields · synced Jun 19, 2026