Diomed Developments Limited
GB-MF-000004862 · United Kingdom · Hitchin
Diomed Developments Limited is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: Doublebase Dry Skin Emollient 100g, Doublebase Dry Skin Emollient 250g, Doublebase Emollient Gel 100g, Doublebase Emollient Gel 25g, Doublebase Once 100g.
Authorised representative in the Union: Acorn Regulatory Consultancy Services Ltd.
Devices declared under this manufacturer
- 4Head QuickStrip
- Doublebase Dry Skin Emollient
- Doublebase Emollient Gel
- Doublebase Once
- Doublebase Once OTC
- Otex Express
- Otex Olive Oil ear drops
- Otex Sodium Bicarbonate
Showing 12 of 14 declared devices.
Catalogue references include 100083, 100120, 100129, 100155, 100199, 100200.
European nomenclature codes declared: M9002, Q030499, M9001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. Diomed Developments Limited was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
40567 | issued | 2030-12-05 |