Plinth Medical Ltd
UK-MF-000057774 · United Kingdom · Suffolk
Plinth Medical Ltd is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: 500 Series.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Plinth Medical
Showing 12 of 24 declared devices.
Catalogue references include 112, 501, 501 2 Sec, 502R, 503, 503AH.
European nomenclature codes declared: V080603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. Plinth Medical Ltd was not found in either the U.S. or the Canadian register.