Identity
- Trade Name
- Protek EUDAMED
- Device Name
- Protek Wrist Splint EUDAMED
- Model / Reference
- 20083 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060483320083 EUDAMED
- Basic UDI-DI
- 50604833TF200B5Z EUDAMED
- EMDN Code
- Y060612 WRIST-HAND ORTHOSES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Northern Ireland 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
Protek by Lightwing Marketing Limited — 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 | 50604833TF200B5Z | Class I | Active |
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Manufacturer
- Manufacturer
- Lightwing Marketing Limited
- EUDAMED SRN
- UK-MF-000046146
- Authorised Representative
- Patient Guard Europe UG DE-AR-000007523
Sources (1)
- EUDAMED ab6e294f-5b82-4277-8126-a86da412f2e3 61 fields · synced Jun 18, 2026