Nagor Limited
GB-MF-000019179 · United Kingdom · Glasgow
Nagor Limited is registered in the European database on medical devices as a manufacturer, with 240 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 168 |
|---|---|
| Class IIa | 66 |
| Class IIb | 6 |
Most frequent device types declared: GS-EHR 460, GS-XM2 370, IMP-MR 330, IMP-SHR 150, IMP-SHR 270.
Among these devices, 240 are declared sterile, 173 implantable.
Authorised representative in the Union: GC Aesthetics (Management) Limited.
Devices declared under this manufacturer
- Nagor Limited
- Nagor Limted
- Nagor limited
Showing 12 of 240 declared devices.
Catalogue references include GS-XM2 370, IMP-MR 330, IMP-SHR 150, IMP-SHR 270, IMP-SHR 560, IMP-SMR 270.
European nomenclature codes declared: P0601010201, P0699, P0601010202, P0601020202, P900103, P080201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 240 |
| 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 | 240 |
|---|---|
| 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. Nagor Limited was not found in either the U.S. or the Canadian register.