Other products from "DIAGNOSTICA STAGO"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 13607450007388 00738 GJT PLASMA, COAGULATION FACTOR DEFICIENT STA® - Deficient X
2 13607450007234 00723 GJT PLASMA, COAGULATION FACTOR DEFICIENT STA® - Deficient XI
3 13607450006145 00614 JCO BOTHROPS ATROX REAGENT STA® - Reptilase®
4 13607450005209 00520 GJT PLASMA, COAGULATION FACTOR DEFICIENT STA® - VWF:Ag Calibrator
5 03607450581041 58104 JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 STA Satellite®
6 03607450009484 00948 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 Asserachrom® tPA
7 03607450009477 00947 DAP FIBRINOGEN AND FIBRIN SPLIT PRODUCTS, ANTIGEN, ANTISERUM, CONTROL 2 Asserachrom® D-Di
8 03607450008579 00857 JBN Fibrin monomer paracoagulation 2 F.S. Test
9 03607450007466 00746 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 STA® - Staclot® Protein S
10 03607450006780 00678 GGN,GGC PLASMA, COAGULATION CONTROL,CONTROL, PLASMA, ABNORMAL 2 STA® - System Control N + P
11 03607450006674 00667 GJS TEST, TIME, PROTHROMBIN 2 STA® - Néoplastine® CI Plus 10
12 03607450006063 00606 GJS TEST, TIME, PROTHROMBIN 2 STA® - Néoplastine® CI Plus 5
13 03607450582307 58230 GKP INSTRUMENT, COAGULATION, AUTOMATED 2 ST art®
14 03607450007374 00737 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 STA® - Staclot® Protein C 3
15 03607450006001 00600 GFO ACTIVATED PARTIAL THROMBOPLASTIN 2 Staclot® LA
16 03607450005943 00594 GFO ACTIVATED PARTIAL THROMBOPLASTIN 2 Staclot® LA 20
17 03607450005684 00568 JBQ ANTITHROMBIN III QUANTITATION 2 Liatest® AT III
18 03607450002010 00201 GGC,GGN CONTROL, PLASMA, ABNORMAL,PLASMA, COAGULATION CONTROL 2 STA® - Control LA 1 + 2
19 13607450007258 00725 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY STA® - Deficient VIII
20 13607450007241 00724 GJT PLASMA, COAGULATION FACTOR DEFICIENT STA® - Deficient IX
21 13607450005414 00541 DAP FIBRINOGEN AND FIBRIN SPLIT PRODUCTS, ANTIGEN, ANTISERUM, CONTROL FDP Plasma (Latex)
22 13607450003335 00333 GIR REAGENT, RUSSEL VIPER VENOM STA® - Staclot® dRVV Screen 5
23 03607450009439 00943 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 Asserachrom® IX:Ag
24 03607450009064 00906 KFF ASSAY, HEPARIN 2 Stachrom® Heparin
25 03607450007473 00747 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 STA® - Staclot® Protein C 1
26 03607450006834 00683 KFF ASSAY, HEPARIN 2 STA® - Heparin Control
27 03607450006773 00677 GGN PLASMA, COAGULATION CONTROL 2 STA® - Coag Control (N + ABN) PLUS
28 03607450006766 00676 GGC,GGN CONTROL, PLASMA, ABNORMAL,PLASMA, COAGULATION CONTROL 2 STA® - Coag Control N + ABN
29 03607450006599 00659 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 STA® - Stachrom® Antiplasmin
30 03607450006582 00658 DDX PLASMINOGEN, ANTIGEN, ANTISERUM, CONTROL 1 STA® - Stachrom® Plasminogen
31 03607450005974 00597 GGW TEST, TIME, PARTIAL THROMBOPLASTIN 2 STA® - C.K. Prest® 5
32 03607450005189 00518 GJT PLASMA, COAGULATION FACTOR DEFICIENT 2 STA® - Liatest® VWF:Ag
33 03607450005165 00516 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 STA® - Liatest® Free Protein S 6
34 03607450004540 00454 GHH FIBRIN SPLIT PRODUCTS 2 D-Di Test®
35 03607450003482 00348 JIS CALIBRATOR, PRIMARY 2 STA® - Multi Hep Calibrator
36 13607450011392 01139 GGN PLASMA, COAGULATION CONTROL Pool Norm
37 13607450007449 00744 GJS,GJT TEST, TIME, PROTHROMBIN,PLASMA, COAGULATION FACTOR DEFICIENT STA® - Deficient V
38 13607450006749 00674 KQJ SYSTEM, FIBRINOGEN DETERMINATION STA® - Fibrinogen 5
39 13607450006114 00611 GJA TEST, THROMBIN TIME STA® - Thrombin 2
40 13607450003670 00367 PPM General purpose reagent STA® - CaCl2 0.025 M
41 03607450590104 59010 JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 STA R Max® (with cap piercing option)
42 03607450011784 00311US KFF ASSAY, HEPARIN 2 STA® - Liquid Anti-Xa 4
43 03607450009514 00951 LCO PLATELET FACTOR 4 RADIOIMMUNOASSAY 2 Asserachrom® PF4
44 03607450009460 00946 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 Asserachrom® Free Protein S
45 03607450009453 00945 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 Asserachrom® Total Protein S
46 03607450009422 00942 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 Asserachrom® VWF:Ag
47 03607450006810 00681 KFF ASSAY, HEPARIN 2 STA® - Hepanorm® HBPM/LMWH
48 03607450006056 00605 GJS TEST, TIME, PROTHROMBIN 2 STA® - Néoplastine® CI 5
49 03607450005400 00540 DAP FIBRINOGEN AND FIBRIN SPLIT PRODUCTS, ANTIGEN, ANTISERUM, CONTROL 2 FDP Plasma
50 03607450589894 58989 JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 STA Compact Max® (with cap piercing option)
Other products with the same Product Code "JPA"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 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.
2 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.
3 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.
4 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.
5 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.
6 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.
7 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.
8 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.
9 30812747018412 07-066 TEG ANALYZER 5000, 230V, 60HZ, FG TEG5000 HEMOSTASIS ANALYZER HAEMONETICS CORPORATION
10 30812747018184 07-022 TEG ANALYZER, 5000, 120V, 60HZ, FG TEG5000 HEMOSTASIS ANALYZER HAEMONETICS CORPORATION
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15 20812747018002 07-004 KAOLIN TEG5000 HEMOSTASIS SYSTEM HAEMONETICS CORPORATION
16 20763000014876 550-13 CONTROL 550-13 CLOTTRAC HR 11L 30PK CLOTtrac™ MEDTRONIC, INC.
17 20763000014814 550-01 CONTROL 550-01 CLOTTRAC CWB 11L 15BX CLOTtrac™ MEDTRONIC, INC.
18 20643169577484 402-02 CARTRIDGE 402-02 ACT RACT 13 LAN RACT MEDTRONIC, INC.
19 20613994531821 402-02 CARTRIDGE 402-02 ACT RACT 14L RACT MEDTRONIC, INC.
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21 20613994130383 550-13 CONTROL 550-13 CLOTTRAC HR 11L 30PK NA MEDTRONIC, INC.
22 15391521421125 DSF Destiny System Fluid TCOAG IRELAND LIMITED
23 15391521420708 T5102 TriniCAL™ Reference Plasma TCOAG IRELAND LIMITED
24 10885074184828 550-01 CONTROL 550-01 CLOTTRAC CWB 11L 15BX CLOTtrac® MEDTRONIC, INC.
25 10812747018463 07-605-US Citrated: K, RT, FF Hemostasis System HAEMONETICS CORPORATION
26 10812747018456 01-197 ELECTRONIC PIPPETTE KIT, 1000UL TEG5000 HAEMONETICS CORPORATION
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30 10812747018142 01-096 PIPETTE KIT, 100UL TEG5000 HAEMONETICS CORPORATION
31 10812747018043 07-012 CALCIUM CHLORIDE, 0.2M, 5 ML TEG HEMOSTASIS SYSTEM HAEMONETICS CORPORATION
32 10711234540121 000GCCM 000GCCM Centralized Configuration Manager Software Centralized Configuration Manager Software ACCRIVA DIAGNOSTICS HOLDINGS, INC.
33 10711234540114 HR1003 HR1003 Temperature Verification Tube Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
34 10711234540107 J-1001 J-1001 Temperature Verification Cartridge Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
35 10711234540091 JEA-QC JEA-QC Electronic System Verification - Abnormal Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
36 10711234540084 JEN-QC JEN-QC Electronic System Verification - Normal Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
37 10711234540077 HE-J04 HE-J04 Electronic System Verification Kit Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
38 10711234540060 HR1003 HR1003 Temperature Verification Tube Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
39 10711234540053 HE-ESV HE-ESV Electronic System Verification Tube Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
40 10711234540039 RPM-CD RPM-CD Report Maker V6.01 Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
41 10711234540022 HRDM3CD HRDM3CD Data Manager V3.0 Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
42 10711234520062 HRS.110-D HRS.110-D Hemochron Whole Blood Coagulation System - Hemochron Response Instrument (Demonstration) Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
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46 10711234515044 000GH100L 000GH100L GEM Hemochron 100 System (Loaner) GEM Hemochron 100 System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
47 10711234515006 000GH100 000GH100 GEM Hemochron 100 System - GEM Hemochron 100 Instrument GEM Hemochron 100 System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
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