Duckworth & Kent Ltd.
GB-MF-000002176 · United Kingdom · Baldock
Duckworth & Kent Ltd. is registered in the European database on medical devices as a manufacturer, with 408 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 408 |
|---|
Most frequent device types declared: 2-522E, 3-201, 3-303, 6-072-1, 6-080-2.
Among these devices, 408 are declared reusable.
Authorised representative in the Union: Emergo Europe B.V..
Catalogue references include 2-522E, 3-303, 6-072-1, 6-080-2, 6-836-2, 6-856.
European nomenclature codes declared: L170201, L1711, L170102, L1799, L1705, L1706.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | DUCKWORTH & KENT, LTD. (GB) · FDA 8021817 |
| Devices in EUDAMED | 408 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 408 |
|---|---|
| Found in the U.S. device database | 407 |
| Share | 99.8 % |
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. Duckworth & Kent Ltd. is registered in the United States but was not found in the Canadian register.