Fairfax Medical Products Limited
GB-MF-000025334 · United Kingdom · London
Fairfax Medical Products Limited is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: STABILOK DENTINE PIN, STABILOK TWIST DRILL.
Among these devices, 8 are declared implantable, 4 reusable, 1 with a measuring function.
Authorised representative in the Union: MD REPS Ltd.
Devices declared under this manufacturer
- STABILOK DENTINE PIN KIT
- STABILOK TWIST DRILL
Catalogue references include BLUE DB, ECONOMY GREEN JG, ECONOMY YELLOW JY, GREEN DG, ORANGE DO, STANDARD ORANGE SO.
European nomenclature codes declared: Q010105, Z12110102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | FAIRFAX MEDICAL PRODUCTS Ltd (GB) · FDA 3004139812 |
| Devices in EUDAMED | 12 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| Found in the U.S. device database | 12 |
| Share | 100.0 % |
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: United States only. Fairfax Medical Products Limited is registered in the United States but was not found in the Canadian register.