The Sonoclot Analyzer is a versatile instrument for measuring coagulation and platelet function in whole blood or plasma. It is used worldwide to manage anticoagulant therapy, assess platelet function, control blood product usage, differentiate mechanical versus hemostatic bleeders, identify hypercoagulable and heparin resistant patients, and screen for hyperfibrinolysis. Clinical areas include open heart surgery, liver transplant surgery, vascular surgery, orthopedic surgery, obstetrics/neonate care, cardiology, trauma and hemostasis research.
The Sonoclot Analyzer incorporates Sienco's patented whole blood viscoelastic clot detection mechanism. It provides effective clinical hemostasis management for operating rooms, coagulation labs, STAT labs, and intensive care units.
Each test analysis provides accurate information on the entire hemostasis process including coagulation, fibrin gel formation, clot retraction (platelet function), and fibrinolysis. The Sonoclot Analyzer generates both a qualitative graph, known as the Sonoclot Signature, and quantitative results on the clot formation time (Activated Clotting Time - Onset) and the rate of fibrin polymerization (Clot RATE). The Onset and Clot RATE results are automatically calculated and appear on the LED display and are printed on the hard copy graphic output.
A powerful tool for patient management, clinical trials, and research. Signature Viewer provides ACT, clot formation rate, and clot retraction results. It allows you to manage data effectively and easily. With Signature Viewer, you can collect signatures from multiple Sonoclot Analyzers, overlay multiple signatures for convenient comparison, export results to spreadsheets or databases, browse hemostasis management libraries, export publiciation quality graphs, and simplify your quality control documentation.
Signature Viewer is both Macintosh and Windows compatible, please contact Sienco for specific minimum system requirements. Licenses for this software are sold in one-copy units. (Sonoclot® Analyzers and personal computer not included.)
Combines a Sonoclot® Coagulation & Platelet Function Analyzer with a one-copy license for the Signature ViewerTM Program into a single package.
Combines Sonoclot® Coagulation & Platelet Function Analyzer and Thermal Printer into a single package.
Provides a permanent, real time record of the "Signature" as it is produced by the Sonoclot® Analyzer. An audible warning is generated if the printer is not properly connected, turned on, or on-line.
Plastic handheld tool for removing used probes.
Reusable aluminum heating block to warm vials. Fits conveniently on Sonoclot Analyzers. (Vials not included.)
Convenient luer cannula tips tp improve control for adding blood to test cuvettes when transfering blood from a syringe.
kACT Kit (800-0400)The kACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The kACT test is a kaolin activated whole blood clotting time test. It may also be used with citrated whole blood and plasma.
The kACT Kit is intended for high dose heparin management with or without aprotinin. The kACT test provides quantitative Onset/ACT and Clot Rate results with the Sonoclot Analyzer. The kACT test is not intended for platelet function monitoring.
gbACT+TM Kit (800-0412)The gbACT+TM Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The gbACT+ test is a glass bead activated whole blood clotting time test. It may also be used with citrated whole blood and plasma.
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 Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.
The gbACT+TM Kit with Fenestrated Probes contains the same gbACT+ test cuvette as the gbACT+ Kit, but contains fenestrated probes in place of the normal probes. The fenestrated probe enhances clot adhesion to the probe. Therefore, it is well suited for use in applications with poor platelet adhesion or hyperfibrinolysis such as liver transplant surgery.
Non-Activated Kit(800-0425)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.
The Non-Activated Kit with Fenestrated probes contains the same Non-Activated cuvettes as the Non-Activated Kit, but has fenestrated probes in place of normal probes. The fenestrated probe enhances clot adhesion to the probe. Therefore, it is well suited for use in applications with poor platelet adhesion or hyperfibrinolysis such as liver transplant surgery.
SonACTTM Kit (800-0432)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.
SonACTTM Kit with Fenestrated Probes (800-0434)
The SonACT Kit with Fenestrated Probes contains the same SonACT test cuvette as the SonACT Kit, but contains fenestrated probes in place of the normal probes. The fenestrated probe enhances clot adhesion to the probe. Therefore, it is well suited for use in applications with poor platelet adhesion or hyperfibrinolysis such as liver transplant surgery.
aiACTTM Kit (800-0441) 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 cadiopulmonary 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.
Prevents crust formation. Recommended for use on tests run over 30 minutes - 1 vial, 20 ml.
Reference Viscosity Oil Quality Control Kit (900-1302)Provides all necessary materials for running two point verification testing of the Sonoclot Analyzer. The kit contains 24 tests.
Reference Plasma Quality Control Kit (900-1318)Provides all necessary materials for running a two level reference plasma test to verify performance of both the Sonoclot Analyzer and activation test reagent. Reference plasma, distilled water, calcium chloride, Non-Activated test cuvettes, probes, and five 1 ml syringes are included. This test is best run with the Plasma QC Heating Block (800-0618).
Plasma Quality Control Heating Block (800-0618)Reusable aluminum heating block to warm quality control reference plasmas. Fits conveniently on Sonoclot Analyzers.
Package of ten 6 ml vials containing a lyophilized preparation of citrated animal plasma, stabilizers, and buffer. Contains no human material.
Package of 6 ml vials containing 5.0 ml laboratory grade distilled water.
Package of ten 6 ml vials containing 5.0 ml 0.02 M Calcium Chloride.
Package of ten 1.0 cc plastic syringes for use with the 800-0618 Plasma Quality Control Heating Block.