Lightwing Marketing Limited
UK-MF-000046146 · United Kingdom · Maidstone
Lightwing Marketing Limited is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: 20083, 20090, 21004, 21103, 21127.
Authorised representative in the Union: Patient Guard Europe UG.
Devices declared under this manufacturer
- Protek
Catalogue references include 20083, 20090, 20106, 21004, 21103, 21127.
European nomenclature codes declared: Y060612, Y06120601, M030501, Y060624, M03050202, Y060699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Lightwing Marketing Limited was not found in either the U.S. or the Canadian register.