Deben Diagnostics Ltd
GB-MF-000023695 · United Kingdom · Ipswich
Deben Diagnostics Ltd is registered in the European database on medical devices as a manufacturer, with 239 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: H-x, O-18, O125, O136, O142.
Authorised representative in the Union: EU-UK Authorised Representative Ltd.
Catalogue references include 293879, 294289, 294371, 295064, 295071, 295699.
European nomenclature codes declared: W01029001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 239 |
| 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 | 239 |
|---|---|
| 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. Deben Diagnostics Ltd was not found in either the U.S. or the Canadian register.