Camstent Ltd
GB-MF-000012349 · United Kingdom · Sharnbrook
Camstent Ltd 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: CSF12S10, CSF12S10T, CSF14S10, CSF14S10T, CSF16F10.
Among these devices, 14 are declared sterile.
Authorised representative in the Union: Medical Device Management Ltd.
Catalogue references include CSF12S10, CSF14S10, CSF16F10, CSF16S10, CSF18F10, CSF18S10T.
European nomenclature codes declared: U010201, U010206.
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. Camstent Ltd was not found in either the U.S. or the Canadian register.