Ennogen Healthcare International Limited
UK-MF-000039877 · United Kingdom · Kent
Ennogen Healthcare International Limited is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Most frequent device types declared: 15g EN/FR.
Authorised representative in the Union: Elara Pharmaservices Europe Ltd.
Devices declared under this manufacturer
- Aquasoothe 1%
- Aquasoothe 2%
- Derma Protective Plus Skin Protectant
- Emulsifying Ointment
- Enopen
- Fifty:50
- Silconex Scar Treatment Gel
- Thirty30
- Thirty:30
Showing 12 of 17 declared devices.
Catalogue references include DERMA115PROTUBE, ENOPENCREAM1050GM, ENOPENCREAM150GM, ENOPENCREAM50GM, FIFTY50OINT500GRAM, SILCONEX15GM.
European nomenclature codes declared: M9002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. Ennogen Healthcare International Limited was not found in either the U.S. or the Canadian register.