Endoscope-i Ltd
UK-MF-000044880 · United Kingdom · Birmingham
Endoscope-i Ltd is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 35 |
|---|
Most frequent device types declared: AGS – PL100.
Among these devices, 1 are declared active.
Authorised representative in the Union: CERT3GLOBAL, UNIPESSOAL, LDA..
Catalogue references include 1601, EILS, ei11, ei13Mini, ei14, ei15.
European nomenclature codes declared: Z12021080, Z12020402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| 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 | 35 |
|---|---|
| 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. Endoscope-i Ltd was not found in either the U.S. or the Canadian register.