Other products from "SYSMEX CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 04987562433698 CN383000 UF-CALIBRATOR JIW Calibrator, surrogate UF-CALIBRATOR
2 14987562460332 213528 XN CAL 5X3.0ML KRX CALIBRATOR FOR CELL INDICES 2 XN CAL
3 04987562444779 CJ445012 Fully Automated Urine Particle Digital Imaging Device UD-10 JOY DEVICE, AUTOMATED CELL-LOCATING 2 Fully Automated Urine Particle Digital Imaging Device UD-10
4 04987562434572 BD634545 Automated Hematology Analyzer XN-L series XN-550 GKZ Counter, differential cell 2 Automated Hematology Analyzer XN-L series XN-550
5 04987562425716 CK978289 Automated Blood Coagulation Analyzer CA-660 GKP INSTRUMENT, COAGULATION, AUTOMATED 2 Automated Blood Coagulation Analyzer CA-600 series CA-660
6 04987562408535 06404310 UF ll CALIBRATOR JIW CALIBRATOR, SURROGATE UF ll CALIBRATOR
7 14987562460387 218981 Range Check X lll 24X3.0ML WBC/RBC/PLT JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 RANGE CHECK X lll
8 14987562508003 CC118360 Platelet CHECK Platelet CHECK Level 2-16x3.0ML GJP Control, Platelet 2 Platelet CHECK
9 14987562507990 CN464998 Platelet CHECK Platelet CHECK Level 1-16x3.0ML GJP Control, Platelet 2 Platelet CHECK
10 04987562440139 BN344411 Fully Automated Urine Particle Analyzer UF-5000 LKM COUNTER, URINE PARTICLE 2 Fully Automated Urine Particle Analyzer UF-5000
11 04987562434534 AW618382 Automated Hematology Analyzer XN-L series XN-350 GKZ Counter, differential cell 2 Automated Hematology Analyzer XN-L series XN-350
12 04987562429219 AR408878 Automated Hematology Analyzer XP-300 GKZ,GKL Counter, differential cell,COUNTER, CELL, AUTOMATED (PARTICLE COUNTER) 2 Automated Hematology Analyzer XP series XP-300
13 04987562412860 BB046392 XS-1000iC Complete GKZ Counter, differential cell 2 Automated Hematology Analyzer XS series XS-1000iC
14 14987562460578 199-5002-0 E-Check (XS) 5X1.5MLX2 Normal/High GLQ,JPK MIXTURE, CONTROL, WHITE-CELL AND RED-CELL INDICES,MIXTURE, HEMATOLOGY QUALITY CONTROL 2 e-CHECK(XS)
15 14987562460561 199-5001-0 E-Check (XS) 5X1.5MLX1 Low JPK,GLQ MIXTURE, HEMATOLOGY QUALITY CONTROL,MIXTURE, CONTROL, WHITE-CELL AND RED-CELL INDICES 2 e-CHECK(XS)
16 04987562434527 CX851950 Automated Hematology Analyzer XN-L series XN-330 GKZ Counter, differential cell 2 Automated Hematology Analyzer XN-L series XN-330
17 04987562433735 BV981798 CS-2500 COMPLETE JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 Automated Blood Coagulation Analyzer CS-2500
18 14987562460356 213537 XN CAL PF 5X3.0ML KRX CALIBRATOR FOR CELL INDICES 2 XN CAL PF
19 04987562424214 AP795756 XN-10 Complete GKZ Counter, differential cell 2 Automated Hematology Analyzer XN series XN-10
20 14987562460349 213536 XN CAL PF 1X3.0ML KRX CALIBRATOR FOR CELL INDICES 2 XN CAL PF
21 04987562434541 CL032175 Automated Hematology Analyzer XN-L series XN-430 GKZ Counter, differential cell 2 Automated Hematology Analyzer XN-L series XN-430
22 04987562432615 CS297931 XN-11 Complete GKZ Counter, differential cell 2 Automated Hematology Analyzer XN series XN-11
23 04987562424221 AE797961 Automated Hematology Analyzer XN series XN-20 GKZ Counter, differential cell 2 Automated Hematology Analyzer XN series XN-20
24 04987562408542 05366719 Sysmex UF-1000i™ Automated Urine Particle Analyzer LKM COUNTER, URINE PARTICLE 2 Fully Automated Urine Particle Analyzer UF-1000i
25 04987562406807 05342311 Sysmex XS-1000i™ Automated Hematology Analyzer GKZ Counter, differential cell 2 Automated Hematology Analyzer XS series XS-1000i
26 14987562460615 200-4004-1 plt-CHECK Level 2- 12X4.5ML JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 plt-CHECK
27 14987562460608 200-4004-0 plt-CHECK Level 1-12X4.5ML JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 plt-CHECK
28 14987562460592 110-4008-0 X-Cal FSR Kit (5X4.6ML) KRX CALIBRATOR FOR CELL INDICES 2 X-CAL Calibrator
29 14987562460585 110-4009-0 X-Cal Hematology Calibrator (4.6ML) KRX CALIBRATOR FOR CELL INDICES 2 X-CAL Calibrator
30 14987562460394 AS747750 XN-L CHECK JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 XN-L CHECK
31 14987562460288 199-4004-1 E-Check 4X4.5MLX3 Low/Normal/High JPK,GLQ MIXTURE, HEMATOLOGY QUALITY CONTROL,MIXTURE, CONTROL, WHITE-CELL AND RED-CELL INDICES 2 e-CHECK
32 04987562434565 BQ391107 Automated Hematology Analyzer XN-L series XN-530 GKZ Counter, differential cell 2 Automated Hematology Analyzer XN-L series XN-530
33 04987562490110 CT129514 Automated Hematology Analyzer XW-100 GKZ Counter, differential cell 2 Automated Hematology Analyzer XW-100
34 04987562434558 BM392756 Automated Hematology Analyzer XN-L series XN-450 GKZ Counter, differential cell 2 Automated Hematology Analyzer XN-L series XN-450
35 04987562402021 02318618 pocH-100i (US) GKZ,GKL Counter, differential cell,COUNTER, CELL, AUTOMATED (PARTICLE COUNTER) 2 Automated Hematology Analyzer pocH-100i
36 14987562460325 213527 XN CAL 1X3.0ML KRX CALIBRATOR FOR CELL INDICES 2 XN CAL
37 14987562460318 213516 XN CHECK BF 6X3.0ML L 1,2 JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 XN CHECK BF
38 14987562460370 217685 SCS-1000 Universal Calibrator 1X2ML KSA CALIBRATOR FOR RED-CELL AND WHITE-CELL COUNTING 2 SCS-1000 Calibrator
39 14987562461797 AX844619 WRP CHECK EX JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 WRP CHECK EX
40 14987562460257 130-4003-0 Range Check X ll JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 RANGE CHECK X ll
41 04987562404087 03309313 Automated Hematology Analyzer XE-2100D GKZ Counter, differential cell 2 Automated Hematology Analyzer XE-2100D
42 14987562502766 NSH-100G BV166979 XN CHECK 8 x 3.0mL, Level 3 JPK Mixture, Hematology Quality Control 2 XN CHECK
43 14987562502759 NSN-100G CV649926 XN CHECK 8 x 3.0mL, Level 2 JPK Mixture, Hematology Quality Control 2 XN CHECK
44 14987562502742 NSL-100G AF640985 XN CHECK 8 x 3.0mL, Level 1 JPK Mixture, Hematology Quality Control 2 XN CHECK
45 14987562490216 BP935764 XW QC CHECK JPK Mixture, hematology quality control 2 XW QC CHECK
46 14987562461780 BG234784 WRP CHECK JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 WRP CHECK
47 14987562460295 201-6001-0 E-Check (XE) 4X4.5MLX3 Levels JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 e-CHECK(XE)
48 14987562460264 140-3004-0 EightCheck-3WP X-tra 4X2MLX3 Lo/Norm/Hi JPK MIXTURE, HEMATOLOGY QUALITY CONTROL 2 EIGHTCHECK-3WP
49 04987562425686 BR142626 Automated Blood Coagulation Analyzer CA-620 JPA,GKP SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES,INSTRUMENT, COAGULATION, AUTOMATED 2 Automated Blood Coagulation Analyzer CA-600 series CA-620
50 04987562409471 06372511 CS-2100i COMPLETE JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 Automated Blood Coagulation Analyzer CS-2100i
Other products with the same Product Code "JPA"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 05391521421081 M01000 Destiny MAX Analyzer TCOAG IRELAND LIMITED
2 05391521421029 H01000P Destiny Plus TCOAG IRELAND LIMITED
3 05391521421012 N04000 KC® 4 Delta TCOAG IRELAND LIMITED
4 05391521421005 G05000 KC® 1 Delta TCOAG IRELAND LIMITED
5 04987562433735 BV981798 CS-2500 COMPLETE Automated Blood Coagulation Analyzer CS-2500 SYSMEX CORPORATION
6 04987562425686 BR142626 Automated Blood Coagulation Analyzer CA-620 Automated Blood Coagulation Analyzer CA-600 series CA-620 SYSMEX CORPORATION
7 04987562425426 BY990757 CS-5100 COMPLETE Automated Blood Coagulation Analyzer CS-5100 SYSMEX CORPORATION
8 04987562409471 06372511 CS-2100i COMPLETE Automated Blood Coagulation Analyzer CS-2100i SYSMEX CORPORATION
9 G0561025161 102516 102516 Lupus Anticoagulant Confirmation Reagent BIO/DATA CORPORATION
10 04260160470587 delta System (US/CA) 201001 The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively. ROTEM® TEM INNOVATIONS GMBH
11 04260160470372 sigma 211000 The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. ROTEM® TEM INNOVATIONS GMBH
12 04260160470358 sigma ROTROL P 555202 The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. ROTEM® TEM INNOVATIONS GMBH
13 04260160470341 sigma ROTROL N 555201 The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. ROTEM® TEM INNOVATIONS GMBH
14 04260160470327 sigma complete + hep 555502 The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. ROTEM® TEM INNOVATIONS GMBH
15 04260160470242 ex-tem® 503-05-US The EXTEM assay is a semi-quantitative in vitro diagnostic assay used to monitor The EXTEM assay is a semi-quantitative in vitro diagnostic assay used to monitor the coagulation process via the extrinsic pathway in citrated whole blood specimens on the ROTEM® delta. Clotting characteristics are described by the functional parameters Clotting Time (CT), Speed of Clot Formation (CFT and alpha angle), Clot Firmness (A20/MCF) and Clot Lysis (LOT, ML, LI(x)). CFT and alpha (Speed of Clot Formation) are complementary parameters and should be used in conjunction with the main parameters Clotting Time (CT) and Clot Firmness (A20/MCF). ROTEM® TEM INNOVATIONS GMBH
16 04260160470112 ROTROL P 503-25-US, 503-25 ROTROL P is a quality control material for monitoring accuracy and precision of ROTROL P is a quality control material for monitoring accuracy and precision of tests carried out on the ROTEM® delta Thromboelastometry System. For in vitro diagnostic use only. ROTEM® TEM INNOVATIONS GMBH
17 04260160470105 ROTROL N 503-24-US, 503-24 ROTROL N is a quality control material for monitoring accuracy and precision of ROTROL N is a quality control material for monitoring accuracy and precision of tests carried out on the ROTEM® delta Thromboelastometry System. For in vitro diagnostic use only. ROTEM® TEM INNOVATIONS GMBH
18 04260160470099 star-tem® 20 503-10-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environ-ment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve – clot firmness over time) and several defined numerical parameters describing the curve quantitatively.The star-tem® reagent is intended for use as recalcification reagent in the NATEM and INTEM assay on the ROTEM® delta. The corresponding assays are described in the NATEM assay application sheet and in the Instructions for Use of the in-tem® reagent (REF 503-02-US), resp. ROTEM® TEM INNOVATIONS GMBH
19 04260160470082 hep-tem® 503-09-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environ-ment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively.The hep-tem® assay is a semi-quantitative in vitro diagnostic assay used to inactivate heparin in patients receiving unfractionated heparin on the ROTEM® delta. To monitor the coagulation process citrated whole blood specimens are used. Clotting characteristics are described by the functional parameters Clotting Time (CT), Speed of Clot Formation (CFT and alpha angle), Clot Firmness (A20/MCF) and Clot Lysis (LOT, ML, LI(x)). ROTEM® TEM INNOVATIONS GMBH
20 04260160470075 fib-tem® 503-06-US The FIBTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® The FIBTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® delta Thromboelastometry System to monitor the clot firmness of citrated whole blood specimens after blocking platelet contribution to the clot firmness. fib-tem® is always used in conjunction with ex-tem®. Clotting characteristics are described by the functional parameter Clot Firmness (A20/MCF). ROTEM® TEM INNOVATIONS GMBH
21 04260160470068 ap-tem® 503-04-US The APTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® d The APTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® delta Thromboelastometry System to monitor the clot firmness of citrated whole blood specimens after blocking hyperfibrinolysis by aprotinin. ap-tem® is always used in conjunction with ex-tem®. Clotting characteristics are described by the functional parameters Clotting Time (CT), Speed of Clot Formation (CFT and alpha angle), Clot Firmness (A20/MCF) and Clot Lysis (LOT, ML, LI(x)). CFT and alpha (Speed of Clot Formation) are complementary parameters and should be used in conjunction with the main parameters Clotting Time (CT) and Clot Firmness (A20/MCF). ROTEM® TEM INNOVATIONS GMBH
22 04260160470044 in-tem® 503-02-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively.The in-tem® assay is a semi-quantitative in vitro diagnostic assay used to monitor the coagulation process via the intrinsic pathway in citrated whole blood specimens on the ROTEM® delta. Clotting characteristics are described by the functional parameters Clotting Time (CT), Speed of Clot Formation (CFT and alpha angle), Clot Firmness (A20/MCF) and Clot Lysis (LOT, ML, LI(x)). ROTEM® TEM INNOVATIONS GMBH
23 04260160470020 delta System 200100-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively. ROTEM® TEM INNOVATIONS GMBH
24 03607450590272 59027 STA R Max® (with cap piercing option) DIAGNOSTICA STAGO
25 03607450590265 59026 STA R Max® DIAGNOSTICA STAGO
26 03607450590135 59013 STA R Max® DIAGNOSTICA STAGO
27 03607450590104 59010 STA R Max® (with cap piercing option) DIAGNOSTICA STAGO
28 03607450589900 58990 STA Compact Max® DIAGNOSTICA STAGO
29 03607450589894 58989 STA Compact Max® (with cap piercing option) DIAGNOSTICA STAGO
30 03607450589795 58979 STA-R Evolution® Expert Series (with cap piercing option) DIAGNOSTICA STAGO
31 03607450589788 58978 STA-R Evolution® Expert Series DIAGNOSTICA STAGO
32 03607450581041 58104 STA Satellite® DIAGNOSTICA STAGO
33 00842768026812 10487098 ORKL19 Standard Human Plasma for the calibration of coagulation and fibrinolysis tests Standard Human Plasma SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
34 00842768024887 10458677 OVKF032 The BFT II Analyzer is a semi-automated device intended for use to determine PT, The BFT II Analyzer is a semi-automated device intended for use to determine PT, APTT and Fibrinogen BFT II Analyzer SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
35 00842768017742 10446684 OWZC39 Washing Solution is used for cleaning the Siemens Healthcare Diagnostics coagula Washing Solution is used for cleaning the Siemens Healthcare Diagnostics coagulation analyzers Washing Solution for Coagulation Analyzers SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
36 00842768014222 10446232 ORHO37 Supplementary Reagent for coagulation tests Calcium Chloride Solution SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
37 00842768012358 10446541 OVMN11 The cuvettes serve coagulation tests as a reaction vessel. Cuvettes for BFT // Analyzer SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
38 00842768012259 10446530 OVKG03 The cuvettes serve coagulation tests as a reaction vessel. BFT II Analyzer Dispo System SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
39 00842768006869 10445989 OPCC03 For calibration of the Berichrom Heparin assay for measurement of unfractionated heparin Berichrom® Heparin UF Calibrator SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
40 00842768006845 10445987 OPCA03 For calibration of the Berichrom Heparin assay for measurement of low molecular For calibration of the Berichrom Heparin assay for measurement of low molecular weight heparin Berichrom® Heparin LMW Calibrator SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
41 00817869020311 SC-125, SC-126, H2O Hemotec Whole Blood Control Kit Large ANALYTICAL CONTROL SYSTEMS INC
42 00817869020274 SC-127 SC-127 Whole Blood Control Level III ANALYTICAL CONTROL SYSTEMS INC
43 00817869020267 SC-126 SC-126 Whole Blood Control Level II ANALYTICAL CONTROL SYSTEMS INC
44 00817869020250 SC-125 SC-125 Whole Blood Control Level I ANALYTICAL CONTROL SYSTEMS INC
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46 00673978519173 550-90 CONTROL TEST 550-90 PROFICIENCY 5L NA MEDTRONIC, INC.
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48 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.
49 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.
50 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.