Other products from "HAEMONETICS CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00812747010057 4.x.x NextGen version 4.x.x MMH SOFTWARE, BLOOD BANK, STAND ALONE PRODUCTS 2 NextGen
2 10812747018159 01-097 PIPETTE KIT, 1000UL JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 TEG5000
3 30812747013875 08150-110-E MCS+ (RBC), LIST NO 08150-110-E GKT Separator, automated, blood cell, diagnostic 2 MCS+
4 30812747018184 07-022 TEG ANALYZER, 5000, 120V, 60HZ, FG JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 TEG5000 HEMOSTASIS ANALYZER
5 00812747010101 3.x.x SafeTrace Tx version 3.x.x MMH Blood Establishment Computer Software and Accessories 2 SafeTrace Tx
6 00812747010033 4.x.x SafeTrace Tx version 4.x.x MMH Blood Establishment Computer Software and Accessories 2 SafeTrace Tx
7 30812747013851 08150-220-E MCS+ (RBC), LIST NO 08150-220-E GKT Separator, automated, blood cell, diagnostic 2 MCS+
8 30812747011673 0694S-00 Plasma Bottles with Saline Adapter KSR CONTAINER, EMPTY, FOR COLLECTION & PROCESSING OF BLOOD & BLOOD COMPONENTS Haemonetics® PCS®2 & NexSys PCS™ Systems
9 20887691002872 732-37M Transfer Bag 1000 ml w/Y Set KSR CONTAINER, EMPTY, FOR COLLECTION & PROCESSING OF BLOOD & BLOOD COMPONENTS 2 Haemonetics Corporation
10 10887691304214 BPFBLA Leukotrap High Efficiency Leukocyte Reduction Filtration System for Red Blood Ce Leukotrap High Efficiency Leukocyte Reduction Filtration System for Red Blood Cells with BPF4 Filter CAK Microfilter, blood transfusion 2 Haemonetics Leukotrap SC RC
11 10887691000581 RCXL1K RCXL1 High Efficiency Leukocyte Redution Filter with Attached Straight Administr RCXL1 High Efficiency Leukocyte Redution Filter with Attached Straight Administration Set for Single Unit Blood Transfusion CAK Microfilter, blood transfusion 2 RCXL1
12 10812747016278 0265F-00 CS5/5+ FASTPACK, 125ML 20µ RES CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5/5+ SYSTEM
13 10812747016261 0260F-00 CS5/5+ FASTPACK,225ML, 20µ RES CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5/5+ SYSTEM
14 10812747015172 0291A-00 CELL SAVER 5/5+ BOWL SET (70ML) CAC Apparatus, Autotransfusion HAEMONETICS CELL SAVER 5/5+ SYSTEM
15 10812747015165 0263A-00 HIGH SPEED CELL SAVER5/5+BOWL SET CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5/5+ SYSTEM
16 10812747012492 09082-00 TPE PROTOCOL/MANUAL,LN09082-00 GKT Separator, automated, blood cell, diagnostic 2 MCS+
17 10812747012485 09081-00 SDP/PLP PROT MANUL,LN 09081-00 GKT Separator, automated, blood cell, diagnostic 2 MCS+
18 10812747011761 00620-CP PLS Harness Set GKT Separator, automated, blood cell, diagnostic 2 Haemonetics® PCS®2 & NexSys PCS™ Systems
19 10812747011754 00620-00 PLS Harness Set GKT Separator, automated, blood cell, diagnostic 2 Haemonetics® PCS®2 & NexSys PCS™ Systems
20 10812747011730 00695-00 PLS Saline Adaptor GKT Separator, automated, blood cell, diagnostic 2 Haemonetics® PCS®2 & NexSys PCS™ Systems
21 30812747019228 0697S-00 Persona™ Plasma Pooling Bottles KSR CONTAINER, EMPTY, FOR COLLECTION & PROCESSING OF BLOOD & BLOOD COMPONENTS 2 Haemonetics® NexSys PCS® System
22 30812747016616 CSE-E-US CELL SAVER ELITE CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
23 00812747010187 4.x.x NexLynk DMS version 4.x.x MMH Blood Establishment Computer Software and Accessories 2 NexLynk DMS
24 00812747010149 3.x.x ElDorado Donor version 3.x.x MMH SOFTWARE, BLOOD BANK, STAND ALONE PRODUCTS 2 ElDorado Donor
25 00812747010132 2.x.x ElDorado Donor 2.x.x MMH SOFTWARE, BLOOD BANK, STAND ALONE PRODUCTS 2 ElDorado Donor
26 20812747016220 00401-00 EXTENSION LINES FRN Pump, Infusion HAEMONETICS R.I.S. SYSTEM
27 10812747016636 CSE-FP-225F CS ELITE FASTPACK, 225ML, 20µ CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
28 10812747016582 CSE-FP-225V CS ELITE FASTPACK,225ML,150µ CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
29 10812747016575 CSE-FP-125V CS ELITE FASTPACK,125ML,150µ CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
30 10812747016568 CSE-B-1000 WASTE BAG, 10L CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
31 10812747016551 CSE-SQ-1000 SEQUESTRATION KIT CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
32 10812747016544 CSE-P-225 CS ELITE PROCESSING KIT (225ML) CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
33 10812747016537 CSE-P-125 CS ELITE PROCESSING KIT (125ML) CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
34 10812747016520 CSE-P-70 CS ELITE PROCESSING KIT (70ML) CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
35 30812747017910 OPA-E-US ORTHOPAT ADVANCE, LN OPA-E-US CAC Apparatus, Autotransfusion 2 HAEMONETICS ORTHOPAT ADVANCE SYSTEM
36 30812747016814 02005-110-EP CS5+,110V ENG, LN02005-110-EP CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5+ SYSTEM
37 00812747010200 3.x.x Donor Doc version 3.x.x MMH Blood Establishment Computer Software and Accessories 2 Donor Doc
38 00812747010194 3.x.x Symphony version 3.x.x MMH Blood Establishment Computer Software and Accessories 2 Symphony
39 00812747010064 1.x.x CDCS version 1.x.x MMH Blood Establishment Computer Software and Accessories 2 CDCS (Cross Donation Check System)
40 30812747012878 09000-220-EW MCS+, 220V, LN09000-220-EW-RU GKT Separator, automated, blood cell, diagnostic 2 HAEMONETICS MCS+ (LN9000) APHERESIS SYSTEM
41 30812747012854 09000-220-E MCS+, 220V ENGL, LN 09000-220-E GKT Separator, automated, blood cell, diagnostic 2 HAEMONETICS MCS+ (LN9000) APHERESIS SYSTEM
42 30812747012816 09000-110-E MCS+ ,110V ENGL, LN 09000-110-E GKT Separator, automated, blood cell, diagnostic 2 HAEMONETICS MCS+ (LN9000) APHERESIS SYSTEM
43 20887691308745 430-40 Leukocyte Reduction Filter System for Red Blood Cells with BPF4 High Efficiency Leukocyte Reduction Filter System for Red Blood Cells with BPF4 High Efficiency Filter, 16-Segment Tubing, Storage Bag and Sample Pouch CAK Microfilter, blood transfusion 2 Leukocyte SC RC
44 10887691001243 SB1E LipiGuard SB Reinfusion Filter for Salvaged Blood CAK Microfilter, blood transfusion 2 LipiGuard SB
45 10887691000550 PXL8Y PXL 8 High Efficiency Leukocyte Reduction Filter for Platelets with Attached Y-T PXL 8 High Efficiency Leukocyte Reduction Filter for Platelets with Attached Y-Type Administration Set CAK Microfilter, blood transfusion 2 PXL 8
46 10887691000536 PXL8C PXL 8 High Efficiency Leukocyte Reduction Filter for Platelets with Attached Extension Set CAK Microfilter, blood transfusion 2 PXL 8
47 10887691000505 PXL12K PXL 12 High Efficiency Leukocyte Reduction Filter with Attached Straight Adminis PXL 12 High Efficiency Leukocyte Reduction Filter with Attached Straight Administration Set CAK Microfilter, blood transfusion 2 PXL 12 High Efficiency Leukocyte Reduction Filter
48 10812747018074 07-016 PLATELETMAPPING ASSAY AA JOZ SYSTEM, AUTOMATED PLATELET AGGREGATION 2 TEG HEMOSTASIS SYSTEM
49 10812747018067 07-015 PLATELETMAPPING ASSAY ADP JOZ SYSTEM, AUTOMATED PLATELET AGGREGATION 2 TEG HEMOSTASIS SYSTEM
50 10812747018050 07-014 PLATELETMAPPING ASSAY ADP & AA JOZ SYSTEM, AUTOMATED PLATELET AGGREGATION 2 TEG HEMOSTASIS SYSTEM
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
45 00817869020007 CR-109 CR-109 .02M Calcium Chloride ANALYTICAL CONTROL SYSTEMS INC
46 00673978519173 550-90 CONTROL TEST 550-90 PROFICIENCY 5L NA MEDTRONIC, INC.
47 00613994615633 313-51 DEVICE 313-51 HEPTRAC ELEC QLT CNTRL CEM HEPtrac® MEDTRONIC, INC.
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.