APA Parafricta Ltd
GB-MF-000006298 · United Kingdom · Thame
APA Parafricta Ltd is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 43 |
|---|
Authorised representative in the Union: European Healthcare & Device Solutions Ltd..
Devices declared under this manufacturer
- Parafricta
Showing 12 of 43 declared devices.
Catalogue references include PFFB-004L, PFFNBN-001, PFFSS-001, PFFSS-002, PFFUG-001M, PFFUG-001XXXL.
European nomenclature codes declared: V0880, V0811, V0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| 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 | 43 |
|---|---|
| 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. APA Parafricta Ltd was not found in either the U.S. or the Canadian register.