Partners for Endoscopy Limited
GB-MF-000021668 · United Kingdom · Stoke on Trent
Partners for Endoscopy Limited is registered in the European database on medical devices as a manufacturer, with 32 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 32 |
|---|
Most frequent device types declared: EndoStream, Khamsin, ScopeFlow.
Among these devices, 20 are declared sterile, 3 active.
Authorised representative in the Union: Advena Limited.
Catalogue references include PFE145, PFE160, PFE230, PFE241s, PFE242, PFE330s.
European nomenclature codes declared: Z12020585,Z12020685, D0899, Z12011311.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 32 |
| 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 | 32 |
|---|---|
| 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. Partners for Endoscopy Limited was not found in either the U.S. or the Canadian register.