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: NL-AR-000000116.
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 |
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1000307203 | supplemented | 2029-06-20 |
1000307201 | supplemented | 2029-06-20 |