Cantor Barnard Limited
GB-MF-000009886 · United Kingdom · Northamptonshire
Cantor Barnard Limited is registered in the European database on medical devices as a manufacturer, with 66 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 66 |
|---|
Among these devices, 15 are declared sterile.
Authorised representative in the Union: Emergo Europe B.V..
Catalogue references include 1, Many.
European nomenclature codes declared: Q02100402, Q0210040102.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CANTOR BARNARD LTD (GB) · FDA 9610790 |
| Devices in EUDAMED | 66 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 66 |
|---|---|
| Found in the U.S. device database | 4 |
| Share | 6.1 % |
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. Cantor Barnard Limited is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
GB23/00000065 | cancelled | 2028-02-10 |