The following products are currently registered and cleared for clinical use under the CE Mark. Please contact Sienco if you are unsure of your country's regulatory requirements. For products currently cleared for clinical use under the U.S. FDA, please visit our Sonoclot USA site.
Sienco manufactures various tests for different applications, including heparin management, platelet function assessment, and differential heparinase testing.
kACT Kit
The kACT Kit is an in vitro diagnostic test for use with Sonoclot® Analyzer Systems. The kACT test is a kaolin activated clotting time test for use with native whole blood and citrated whole blood.
The kACT Kit is intended for high dose heparin management and provides quantitative ACT and Clot Rate results. The kACT test is not intended for platelet function monitoring.
Available in package sizes of 24 (800-0401) and 100 (800-0400).
gbACT Kit
The gbACT Kit is an in vitro diagnostic test for use with Sonoclot® Analyzer Systems. The gbACT test is a glass bead activated clotting time test for use with native whole blood and citrated whole blood.
The gbACT+ Kit is intended for general purpose global hemostasis monitoring. The monitoring information is typically used for anticoagulant management at low to moderate heparin levels (0 to 2 units per ml), hypercoagulable and/or hypocoagulable screening, and hyperfibrinolysis screening The gbACT test provides quantiative ACT and Clot Rate results. The gbACT test is not intended for high does heparin management during cardiopulmonary bypass surgery or for platelet function assessment.
Available in package sizes of 24 (800-0416) and 100 (800-0410).
gbACT+ Kit
The gbACT+ Kit is an in vitro diagnostic test for use with Sonoclot® Coagulation & Platelet Function Analyzers. The gbACT+ test is a glass bead activated clotting time test for use with native whole blood and citrated whole blood.
The gbACT+ Kit is intended for general purpose global hemostasis monitoring including: clot detection, fibrin formation, platelet function, and hyperfibrinolysis. The monitoring information is typically used for anticoagulant management at low to moderate heparin levels (0 to 2 units per ml), hypercoagulable and/or hypocoagulable screening, platelet function assessment, and hyperfibrinolysis screening.
When used with the Sonoclot Analyzer System, the gbACT+ test provides quantitative ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.
Available in package sizes of 24 (800-0411) and 100 (800-0412).
H-gbACT+ Kit
The H-gbACT+ test is a glass bead activated clotting time test with added heparinase capable of neutralizing up to 5 units/ml of heparin. This test is ideal for post-protamine hemostasis monitoring and in cases where small amounts of residual heparin may prolong a normal glass bead test, impeding platelet function monitoring. It may be used with native whole blood and citrated whole blood.
The H-gbACT+ Kit is intended for general purpose global hemostasis monitoring including: clot detection, fibrin formation, platelet function, and hyperfibrinolysis. Use alongside the gbACT+ test on a SCP2 Sonoclot Analyzer for differential heparinase results.
Available in package sizes of 20 (800-0449) and 50 (800-0448).
Non-Activated Clotting Test Kit
The Non-Activated Clotting Test Kit contains the necessary components for an in vitro diagnostic test for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The Non-Activated Clotting Test is the foundation for a whole blood clotting time test. It may also be used with citrated whole blood and plasma.
The Non-Activated kit is intended for customer designed hemostasis monitoring on the Sonoclot Analyzer. The Non-Activated cuvette allows for coagulation monitoring using tissue activation, thrombin activation, and other custom activators. Some of the applications for the Non-Activated test with the addition of customer determined reagents are monitoring of fibrin formation, fibrinolysis, hyperfibrinolysis and clot retraction. It is mainly a research tool.
When used with the Sonoclot Analyzer System, the Non-Activated test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.
Available in package sizes of 24 (800-0426) and 100 (800-0425).
SonACT™ Kit
The SonACTTM Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The SonACT test is a celite activated whole blood clotting time test. It may also be used with citrated whole blood and plasma.
The SonACT Kit is intended for general purpose global hemostasis monitoring including: clot detection, fibrin formation, platelet function, and hyperfibrinolysis. The monitoring information is typically used for anticoagulant management up to high heparin levels (0 to approximately 6 units per ml), hypercoagulable and/or hypocoagulable screening, platelet function assessment, and hyperfibrinolysis screening.
When used with the Sonoclot Analyzer System, the SonACT test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.
Available in package sizes of 24 (800-0431) and 100 (800-0432).
aiACT Kit
The aiACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The aiACT test is an activated whole blood clotting time test which uses a proprietary blend of celite and other minerals for contact activation. It may also be used with citrated whole blood.
The aiACT Kit is intended for high dose heparin anticoagulation management as typically encountered during cardiopulmonary bypass surgery. The aiACT test provides ACT results that are substantially unaffected by aprotinin. When used with the Sonoclot Analyzer System, the aiACT test provides quantitative Onset/ACT and Clot Rate Results. The aiACT test is not intended for platelet function assessment.
Available in package sizes of 24 (800-0441) and 100 (800-0442).