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: 6-836-2, 6-072-1, 9-599, 6-080-2, 6-870.
Among these devices, 408 are declared reusable.
Authorised representative in the Union: NL-AR-000000116.
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 |