Cerus Endovascular, Ltd.
GB-MF-000008548 · United Kingdom · Oxford
Cerus Endovascular, Ltd. is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class I | 9 |
|---|---|
| Class IIa | 1 |
Most frequent device types declared: 0850014958CNSPFVZ, 0858644007CAB86.
Among these devices, 10 are declared sterile, 9 implantable.
Authorised representative in the Union: Emergo Europe B.V..
Devices declared under this manufacturer
- Cable Set
- Contour 021
- Contour Neurovascular System
- Neqstent
- Neqstent 021
Catalogue references include CAB701-01, CNS011-15, CNS014-15, CNS21005-15, CNS21007-15, NQS21407-15.
European nomenclature codes declared: C010404020299, C010402020399.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CERUS ENDOVASCULAR, INC. (US) · FDA 3013408612 |
| Devices in EUDAMED | 10 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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. Cerus Endovascular, Ltd. is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1000307203 | supplemented | 2029-06-20 |
1000307201 | supplemented | 2029-06-20 |