Medfor Products Ltd
GB-MF-000022996 · United Kingdom · ALDERSHOT
Medfor Products 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 |
|---|
Among these devices, 35 are declared sterile.
Authorised representative in the Union: Emergo Europe B.V..
Catalogue references include OWE0050D-K, OWE1000D-K, OWE2000D-K, S152-K, SKA0500Z-K, SKC0500Z-K.
European nomenclature codes declared: A090199.
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. Medfor Products Ltd was not found in either the U.S. or the Canadian register.