| 109676-001 |
Solent Proxi Thrombectomy Set |
AngioJet Ultra |
|
|
|
| 104834-002 |
Power Pulse Kit |
AngioJet Ultra |
| System Compatibility |
Ultra System |
| Delivery Platform |
OTW |
| Minimum Vessel Diameter |
3mm |
| Working Length |
90cm |
| Shaft Diameter |
6F |
| Wire Compatibility |
0.035" |
| Guide Compatibility |
8F ≥ 0.086" |
| Sheath Compatibility |
6F |
| Marker Bands |
15mm |
| Guide Wire Swappable |
Yes |
The AngioJet System includes several catheter models that are marketed for thrombectomy of coronary arteries and bypass grafts, AV access conduits, peripheral veins and peripheral arteries. See product Information for Use for specific and complete prescribing information.
Operation of the catheter may cause hemolysis. Hemolysis indicators in the blood should be monitored and total catheter activation time should not exceed 8 minutes in a static blood field or 4 minutes in a flowing blood field. Excessive hemolysis may require blood transfusion. In investigational clinical studies, hemolysis induced by AngioJet Thrombectomy was not associated with any significant systemic response.