Kuros Biosciences
NL-MF-000010905 · Netherlands · Bilthoven
Kuros Biosciences is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class I | 44 |
|---|
Most frequent device types declared: 703-001, 703-002, 703-009, 703-015, 703-016.
Among these devices, 44 are declared sterile, 44 implantable.
Catalogue references include 703-009, 703-015, 703-016, 703-021, 703-029, 703-032.
European nomenclature codes declared: P900402.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Kuros Biosciences BV (NL) · FDA 3008147766 |
| Devices in EUDAMED | 44 |
| Country of registration | Netherlands |
Device-level evidence
| Devices with a numeric GTIN | 44 |
|---|---|
| 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: United States only. Kuros Biosciences is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
2248488CE01 | amended | 2030-12-01 |