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Luxtec Bluez Lt Frame In Case
EUDAMEDClass I (EU MDR)
Ref 2199-P-1658
by Keeler Ltd
Identity
- Trade Name
- LUXTEC BLUEZ LT FRAME IN CASE EUDAMED
- Device Name
- Loupes and frames EUDAMED
- Model / Reference
- 2199-P-1658 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055272714648 EUDAMED
- Basic UDI-DI
- 50552727LOUPEFRAMEDB EUDAMED
- Direct Marketing DI
- 05055272714648 EUDAMED
- EMDN Code
- Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I 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
Luxtec Bluez Lt Frame In Case 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 | 50552727LOUPEFRAMEDB | 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 889e7a0f-108d-4ee4-ae73-be0648aaccb0 61 fields · synced Jul 16, 2026