OAKMED LTD
UK-MF-000051482 · United Kingdom · Northampton
OAKMED LTD is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 23 |
|---|
Authorised representative in the Union: Specculo Limited.
Devices declared under this manufacturer
- Oakmed
Showing 12 of 23 declared devices.
Catalogue references include AHP11C10, LPSCA40-0420K, LPSCA40-4115KV, LPSCA47-0420K, SCA25-4120KV, SCA35-4115KVBK.
European nomenclature codes declared: A1001010202,A1001020202,A1001030202, A1001010102,A1001020102,A1001030102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| 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 | 23 |
|---|---|
| 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. OAKMED LTD was not found in either the U.S. or the Canadian register.