NEXA Medical Limited
GB-MF-000021667 · United Kingdom · Bournemouth
NEXA Medical Limited is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 3 |
|---|---|
| Class IIb | 8 |
Most frequent device types declared: 414-00-102, 414-00-111, 414-00-300, 414-00-501, 414-00-502.
Among these devices, 8 are declared sterile.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- NEXA Device Kit
- NEXA Drape
- NEXA Drape, Box of 10
- NEXA Dressing -125mmHg
- NEXA Dressing -125mmHg, Box of 5
- NEXA Dressing -75mmHg
- NEXA Dressing -75mmHg, Box of 5
- NEXA Fluid Container Pack
- NEXA Fluid Container Pack, Box of 5
- NEXA Foam
- NEXA Foam, Box of 5
Catalogue references include 414-00-102, 414-00-111, 414-00-300, 414-00-502, 414-00-511, 414-00-601.
European nomenclature codes declared: Z12019003.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| Found in the U.S. device database | 9 |
| Share | 81.8 % |
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. NEXA Medical Limited was not found in either the U.S. or the Canadian register.