Other products from "TCOAG IRELAND LIMITED"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 15391521420326 T1204 GIT Reagent & Control, Partial Thromboplastin Time TriniCLOT™ aPTT HS 3 mL
2 15391521420234 T1101 GJS Test, Time, Prothrombin TriniCLOT™ PT HTF 20 mL
3 15391521420432 T1511 GJT Plasma, Coagulation Factor Deficient TriniCLOT™ Factor XI
4 15391521420319 T1203 GIT Reagent & Control, Partial Thromboplastin Time TriniCLOT™ aPTT HS 10 mL
5 05391521420305 T1202 GFO Activated Partial Thromboplastin 2 TriniCLOT™ aPTT S 3 mL
6 15391521420425 T1510 GJT Plasma, Coagulation Factor Deficient TriniCLOT™ Factor X
7 15391521420418 T1509 GJT Plasma, Coagulation Factor Deficient TriniCLOT™ Factor IX
8 15391521420821 T1414 KQJ System, Fibrinogen Determination TriniCLOT™ Thrombin Time 4ml
9 15391521420722 T5104 KQJ System, Fibrinogen Determination TriniCAL™ Fibrinogen
10 15391521420661 T4203 GGC Control, Plasma, Abnormal TriniCHECK™ Lupus Positive Control
11 15391521420487 T1605 GIR Reagent, Russel Viper Venom TriniCLOT Lupus Confirm
12 15391521420470 T1604 GIR Reagent, Russel Viper Venom TriniCLOT Lupus Screen
13 15391521420449 T1512 GJT Plasma, Coagulation Factor Deficient TriniCLOT™ Factor XII
14 15391521420364 T1302 KQJ System, Fibrinogen Determination TriniCLOT™ Fibrinogen 6 mL
15 15391521420340 T1206 GFO Activated Partial Thromboplastin TriniCLOT™ Automated aPTT 3 mL
16 15391521420241 T1102 GJS Test, Time, Prothrombin TriniCLOT™ PT HTF 6 mL
17 15391521420081 50705 GHR Reagent, Platelet Aggregation Ristocetin (7.5 mg/vial)
18 05391521420916 T6003 GGP Test, Qualitative And Quantitative Factor Deficiency 2 TriniLIZE™ PAI-1 Antigen
19 15391521420760 T3000 GHH Fibrin Split Products TriniLIA™ D-Dimer Saline
20 15391521421309 DTW PPM General Purpose Reagent DT Wash
21 15391521420784 T4304 DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control TriniCHECK™ D-Dimer 2
22 05391521421005 G05000 JPA System, Multipurpose For In Vitro Coagulation Studies 2 KC® 1 Delta
23 05391521420909 T6004 GGP Test, Qualitative And Quantitative Factor Deficiency 2 TriniLIZE™ PAI-1 Activity
24 05391521420534 T2602 JBQ Antithrombin Iii Quantitation 2 TriniCHROM™ Antithrombin IIa
25 15391521420791 T4305 DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control TriniCHECK™ D-Dimer 3
26 15391521420500 T1901 KQJ System, Fibrinogen Determination TriniCLOT™ Imidazole Buffer
27 15391521420333 T1205 GFO Activated Partial Thromboplastin TriniCLOT™ Automated aPTT 6 mL
28 15391521420777 T4303 GIZ Plasma, Control, Normal TriniCHECK™ D-Dimer 1
29 05391521420718 T5103 DDF Prothrombin, Antigen, Antiserum, Control 1 TriniVerical™
30 05391521420541 T2603 JBQ Antithrombin Iii Quantitation 2 TriniCHROM™ Antithrombin Xa
31 05391521420466 T1602 GGP Test, Qualitative And Quantitative Factor Deficiency 2 TriniCLOT™ Protein S
32 05391521420282 T1106 GJS Test, Time, Prothrombin 2 TriniCLOT™ PT Excel 6 mL
33 05391521420091 50710 GGP Test, Qualitative And Quantitative Factor Deficiency 2 Lyophilized Platelets
34 15391521420401 T1508 GJT Plasma, Coagulation Factor Deficient TriniCLOT™ Factor VIII
35 15391521420388 T1505 GJT Plasma, Coagulation Factor Deficient TriniCLOT™ Factor V
36 15391521421729 DTF PPM General Purpose Reagent DT Fluid
37 15391521421125 DSF JPA System, Multipurpose For In Vitro Coagulation Studies Destiny System Fluid
38 15391521420814 T1411 KQJ System, Fibrinogen Determination TriniCLOT™ Thrombin Time 1ml
39 15391521420647 T4112 OHQ Multi-Analyte Controls Unassayed TriniCHECK Level 2
40 05391521421029 H01000P JPA System, Multipurpose For In Vitro Coagulation Studies 2 Destiny Plus
41 05391521421012 N04000 JPA System, Multipurpose For In Vitro Coagulation Studies 2 KC® 4 Delta
42 05391521420572 T3101 DAP Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control 2 TriniLIA™ D-Dimer
43 05391521420299 T1201 GFO Activated Partial Thromboplastin 2 TriniCLOT™ aPTT S 10 mL
44 05391521420268 T1104 GJS Test, Time, Prothrombin 2 TriniCLOT™ PT Excel S 6 mL
45 05391521420251 T1103 GJS Test, Time, Prothrombin 2 TriniCLOT™ PT Excel S 20 mL
46 15391521420395 T1507 GJT Plasma, Coagulation Factor Deficient TriniCLOT™ Factor VII
47 15391521420630 T4111 OHQ Multi-Analyte Controls Unassayed TriniCHECK Level 1
48 05391521420565 T2608 GGP Test, Qualitative And Quantitative Factor Deficiency 2 TriniCHROM™ Factor VIII:C
49 05391521420350 T1301 KQJ System, Fibrinogen Determination 2 TriniCLOT™ Fibrinogen Kit
50 15391521420708 T5102 JPA System, Multipurpose For In Vitro Coagulation Studies TriniCAL™ Reference Plasma
Other products with the same Product Code "JPA"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00673978519173 550-90 CONTROL TEST 550-90 PROFICIENCY 5L NA MEDTRONIC, INC.
2 00613994615633 313-51 DEVICE 313-51 HEPTRAC ELEC QLT CNTRL CEM HEPtrac® MEDTRONIC, INC.
3 B55890013181 900-1318 900-1318 The Reference Plasma Quality Control Kit is for use with the Sonoclot® Analyzer The Reference Plasma Quality Control Kit is for use with the Sonoclot® Analyzer System to verify performance of activated cuvettes. Testing should be performed prior to the use of a new shipment of activated cuvettes and monthly throughout use of the stock. More frequent testing may be required to comply with local, state and federal QC requirements. Reference plasma quality control is important to properly verify proper performance of coagulation test activators. A two level testing approach is used to perform quality control of the activator used in an activated coagulation test. Level I is run with the activator on the reference plasma. Level II is run with the non-activated test on the reference plasma. These two tests confirm the effectiveness of the activator to perform its intended coagulation activation.Each Kit contains:1 vial Reference Plasma Control - 6 ml vial containing a lyophilized preparation of citrated animal plasma, stabilizers and buffer. Contains no human material.1 vial Distilled Water - 6 ml vial containing 5.0 ml laboratory grade distilled water.1 vial 0.02 M Calcium Chloride - 6 ml vial containing 5.0 ml 0.02 M Calcium Chloride.5 plastic 1 ml syringes2 non-activated test cuvettes (blue with clear caps, stir bars, and probes) Sonoclot® Reference Plasma Quality Control Kit SIENCO, INC.
4 B55890013021 900-1302 900-1302 The Reference Viscosity Oil QC test is a simple means of verifying proper operat The Reference Viscosity Oil QC test is a simple means of verifying proper operation of the Sonoclot Analyzer. This test consists of a two point verification of the electromechanical oscillator and also ensures that the heating control is operating accurately. The two verification points are: 1) Probe-In-Air, and 2) Probe-In-Oil. The Probe-In-Air is the response of the electromechanical oscillator to air. The Probe-In-Oil is the response of the electromechanical oscillator to the reference viscosity liquid. Since the viscosity of the reference viscosity fluid is significantly temperature dependent, the Probe-In-Oil test point also verifies the temperature regulation. The QC test should be run each day the Sonoclot Analyzer is used or as required by your institution. Each Reference Viscosity Quality Control Kit contains 24 cuvettes, 24 probes, 1 vial of reference viscosity oil with end cap, and these instructions. These supplies provide 24 QC tests for the analyzer. Sonoclot® Reference Viscosity Oil Quality Control Kit SIENCO, INC.
5 B55880004321 800-0432 800-0432 The SonACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coag The SonACT 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.Each kit contains 100 lidded colorless plastic activation cuvettes, 100 probes, and instructions for use. The activation cuvettes contain a controlled amount of celite and a magnetic stir bar. Sonoclot® SonACT Kit SIENCO, INC.
6 B55880004311 800-0431 800-0431 The SonACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coag The SonACT 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.Each kit contains 24 lidded colorless plastic activation cuvettes, 24 probes, and instructions for use. The activation cuvettes contain a controlled amount of celite and a magnetic stir bar. Sonoclot® SonACT Kit SIENCO, INC.
7 B55880004261 800-0426 800-0426 The Non-Activated Clotting Test Kit contains the necessary components for an in 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. It may be used with native whole blood, citrated whole blood, and plasma. The Non-Activated Kit may either be used as a non-activated clotting test or as a general use test with user provided activators. It 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. 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. Each kit contains 24 lidded plastic cuvettes, 24 probes, and instructions for use. The cuvettes contain a magnetic stir bar. Sonoclot® NonActivated Kit SIENCO, INC.
8 B55880004251 800-0425 800-0425 The Non-Activated Clotting Test Kit contains the necessary components for an in 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. It may be used with native whole blood, citrated whole blood, and plasma. The Non-Activated Kit may either be used as a non-activated clotting test or as a general use test with user provided activators. It 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. 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. Each kit contains 100 lidded plastic cuvettes, 100 probes, and instructions for use. The cuvettes contain a magnetic stir bar. Sonoclot® NonActivated Kit SIENCO, INC.
9 B55880004011 800-0401 800-0401 The kACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulat The kACT Kit is an in vitro diagnostic test 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. Each kit contains 24 lidded blue plastic activation cuvettes, 24 probes, and instructions for use. The activation cuvettes contain a controlled amount of kaolin and a magnetic stir bar. Sonoclot® kACT Kit SIENCO, INC.
10 B55880004001 800-0400 800-0400 The kACT Kit is an in vitro diagnostic test for use with the Sonoclot Coagulatio The kACT Kit is an in vitro diagnostic test 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.Each kACT Kit contains 100 lidded blue plastic activation cuvettes, 100 probes, and instructions for use. The activation cuvettes contain a controlled amount of kaolin and a magnetic stir bar. Sonoclot® kACT Kit SIENCO, INC.
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18 20763000014876 550-13 CONTROL 550-13 CLOTTRAC HR 11L 30PK CLOTtrac™ MEDTRONIC, INC.
19 20763000014814 550-01 CONTROL 550-01 CLOTTRAC CWB 11L 15BX CLOTtrac™ MEDTRONIC, INC.
20 20643169577484 402-02 CARTRIDGE 402-02 ACT RACT 13 LAN RACT MEDTRONIC, INC.
21 20613994531821 402-02 CARTRIDGE 402-02 ACT RACT 14L RACT MEDTRONIC, INC.
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23 20613994130383 550-13 CONTROL 550-13 CLOTTRAC HR 11L 30PK NA MEDTRONIC, INC.
24 15391521421125 DSF Destiny System Fluid TCOAG IRELAND LIMITED
25 15391521420708 T5102 TriniCAL™ Reference Plasma TCOAG IRELAND LIMITED
26 10885074184828 550-01 CONTROL 550-01 CLOTTRAC CWB 11L 15BX CLOTtrac® MEDTRONIC, INC.
27 10812747018463 07-605-US Citrated: K, RT, FF Hemostasis System HAEMONETICS CORPORATION
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30 10812747018203 07-044 STARTER KIT, TEG5000 TEG5000 HAEMONETICS CORPORATION
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32 10812747018142 01-096 PIPETTE KIT, 100UL TEG5000 HAEMONETICS CORPORATION
33 10812747018043 07-012 CALCIUM CHLORIDE, 0.2M, 5 ML TEG HEMOSTASIS SYSTEM HAEMONETICS CORPORATION
34 10711234540121 000GCCM 000GCCM Centralized Configuration Manager Software Centralized Configuration Manager Software ACCRIVA DIAGNOSTICS HOLDINGS, INC.
35 10711234540114 HR1003 HR1003 Temperature Verification Tube Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
36 10711234540107 J-1001 J-1001 Temperature Verification Cartridge Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
37 10711234540091 JEA-QC JEA-QC Electronic System Verification - Abnormal Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
38 10711234540084 JEN-QC JEN-QC Electronic System Verification - Normal Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
39 10711234540077 HE-J04 HE-J04 Electronic System Verification Kit Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
40 10711234540060 HR1003 HR1003 Temperature Verification Tube Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
41 10711234540053 HE-ESV HE-ESV Electronic System Verification Tube Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
42 10711234540039 RPM-CD RPM-CD Report Maker V6.01 Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
43 10711234540022 HRDM3CD HRDM3CD Data Manager V3.0 Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
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