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Riester Api Ii Led Wireless
EUDAMEDClass I (EU MDR)
Ref 1205-P-2005
by Keeler Ltd
Identity
- Trade Name
- RIESTER API II LED WIRELESS EUDAMED
- Device Name
- Indirect Ophthalmoscope EUDAMED
- Model / Reference
- 1205-P-2005 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055272712620 EUDAMED
- Basic UDI-DI
- 50552727INDOSCOPES5Q EUDAMED
- Direct Marketing DI
- 05055272712620 EUDAMED
- EMDN Code
- Z12120114 OPHTHALMOSCOPES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Riester Api Ii Led Wireless 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 | 50552727INDOSCOPES5Q | 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 a5c9ba9d-90b7-4f5e-a91d-d447e3f03b9e 61 fields · synced Jul 8, 2026