Ennogen Healthcare Ltd
GB-MF-000022280 · United Kingdom · Dartford
Ennogen Healthcare Ltd is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Most frequent device types declared: Thirty:30 125g.
Authorised representative in the Union: Elara Pharmaservices Europe Ltd.
Devices declared under this manufacturer
- Aquasoothe 1% 100g
- Aquasoothe 1% 500g
- Aquasoothe 2% 500g
- Derma Protective Plus
- Emulsifying Ointment
- Enopen 1050g
- Enopen 150g
- Enopen 500g
- Enopen 50g
- Fifty:50 Ointment 250g
- Fifty:50 Ointment 500g
- Thirty:30 125g
Showing 12 of 13 declared devices.
Catalogue references include AQUA1CREAM500GRAM, AQUA2CREAM500GRAM, ENOPENCREAM1050GM, ENOPENCREAM150GM, ENOPENCREAM50GM, FIFTY50OINT250GRAM.
European nomenclature codes declared: M9002, T0499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| 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 | 13 |
|---|---|
| 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 Ltd was not found in either the U.S. or the Canadian register.