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 30812747018412 07-066 TEG ANALYZER 5000, 230V, 60HZ, FG JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 TEG5000 HEMOSTASIS ANALYZER
5 30812747018184 07-022 TEG ANALYZER, 5000, 120V, 60HZ, FG JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 TEG5000 HEMOSTASIS ANALYZER
6 00812747010101 3.x.x SafeTrace Tx version 3.x.x MMH Blood Establishment Computer Software and Accessories 2 SafeTrace Tx
7 00812747010033 4.x.x SafeTrace Tx version 4.x.x MMH Blood Establishment Computer Software and Accessories 2 SafeTrace Tx
8 30812747013851 08150-220-E MCS+ (RBC), LIST NO 08150-220-E GKT Separator, automated, blood cell, diagnostic 2 MCS+
9 30812747011673 0694S-00 Plasma Bottles with Saline Adapter KSR CONTAINER, EMPTY, FOR COLLECTION & PROCESSING OF BLOOD & BLOOD COMPONENTS Haemonetics® PCS®2 & NexSys PCS™ Systems
10 20887691002872 732-37M Transfer Bag 1000 ml w/Y Set KSR CONTAINER, EMPTY, FOR COLLECTION & PROCESSING OF BLOOD & BLOOD COMPONENTS 2 Haemonetics Corporation
11 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
12 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
13 10812747016278 0265F-00 CS5/5+ FASTPACK, 125ML 20µ RES CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5/5+ SYSTEM
14 10812747016261 0260F-00 CS5/5+ FASTPACK,225ML, 20µ RES CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5/5+ SYSTEM
15 10812747015172 0291A-00 CELL SAVER 5/5+ BOWL SET (70ML) CAC Apparatus, Autotransfusion HAEMONETICS CELL SAVER 5/5+ SYSTEM
16 10812747015165 0263A-00 HIGH SPEED CELL SAVER5/5+BOWL SET CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5/5+ SYSTEM
17 10812747012492 09082-00 TPE PROTOCOL/MANUAL,LN09082-00 GKT Separator, automated, blood cell, diagnostic 2 MCS+
18 10812747012485 09081-00 SDP/PLP PROT MANUL,LN 09081-00 GKT Separator, automated, blood cell, diagnostic 2 MCS+
19 10812747011761 00620-CP PLS Harness Set GKT Separator, automated, blood cell, diagnostic 2 Haemonetics® PCS®2 & NexSys PCS™ Systems
20 10812747011754 00620-00 PLS Harness Set GKT Separator, automated, blood cell, diagnostic 2 Haemonetics® PCS®2 & NexSys PCS™ Systems
21 10812747011730 00695-00 PLS Saline Adaptor GKT Separator, automated, blood cell, diagnostic 2 Haemonetics® PCS®2 & NexSys PCS™ Systems
22 30812747019228 0697S-00 Persona™ Plasma Pooling Bottles KSR CONTAINER, EMPTY, FOR COLLECTION & PROCESSING OF BLOOD & BLOOD COMPONENTS 2 Haemonetics® NexSys PCS® System
23 30812747016616 CSE-E-US CELL SAVER ELITE CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
24 00812747010187 4.x.x NexLynk DMS version 4.x.x MMH Blood Establishment Computer Software and Accessories 2 NexLynk DMS
25 00812747010149 3.x.x ElDorado Donor version 3.x.x MMH SOFTWARE, BLOOD BANK, STAND ALONE PRODUCTS 2 ElDorado Donor
26 00812747010132 2.x.x ElDorado Donor 2.x.x MMH SOFTWARE, BLOOD BANK, STAND ALONE PRODUCTS 2 ElDorado Donor
27 20812747016220 00401-00 EXTENSION LINES FRN Pump, Infusion HAEMONETICS R.I.S. SYSTEM
28 10812747016636 CSE-FP-225F CS ELITE FASTPACK, 225ML, 20µ CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
29 10812747016582 CSE-FP-225V CS ELITE FASTPACK,225ML,150µ CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
30 10812747016575 CSE-FP-125V CS ELITE FASTPACK,125ML,150µ CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
31 10812747016568 CSE-B-1000 WASTE BAG, 10L CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
32 10812747016551 CSE-SQ-1000 SEQUESTRATION KIT CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
33 10812747016544 CSE-P-225 CS ELITE PROCESSING KIT (225ML) CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
34 10812747016537 CSE-P-125 CS ELITE PROCESSING KIT (125ML) CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
35 10812747016520 CSE-P-70 CS ELITE PROCESSING KIT (70ML) CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER ELITE SYSTEM
36 30812747017910 OPA-E-US ORTHOPAT ADVANCE, LN OPA-E-US CAC Apparatus, Autotransfusion 2 HAEMONETICS ORTHOPAT ADVANCE SYSTEM
37 30812747016814 02005-110-EP CS5+,110V ENG, LN02005-110-EP CAC Apparatus, Autotransfusion 2 HAEMONETICS CELL SAVER 5+ SYSTEM
38 00812747010200 3.x.x Donor Doc version 3.x.x MMH Blood Establishment Computer Software and Accessories 2 Donor Doc
39 00812747010194 3.x.x Symphony version 3.x.x MMH Blood Establishment Computer Software and Accessories 2 Symphony
40 00812747010064 1.x.x CDCS version 1.x.x MMH Blood Establishment Computer Software and Accessories 2 CDCS (Cross Donation Check System)
41 30812747012878 09000-220-EW MCS+, 220V, LN09000-220-EW-RU GKT Separator, automated, blood cell, diagnostic 2 HAEMONETICS MCS+ (LN9000) APHERESIS SYSTEM
42 30812747012854 09000-220-E MCS+, 220V ENGL, LN 09000-220-E GKT Separator, automated, blood cell, diagnostic 2 HAEMONETICS MCS+ (LN9000) APHERESIS SYSTEM
43 30812747012816 09000-110-E MCS+ ,110V ENGL, LN 09000-110-E GKT Separator, automated, blood cell, diagnostic 2 HAEMONETICS MCS+ (LN9000) APHERESIS SYSTEM
44 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
45 10887691001243 SB1E LipiGuard SB Reinfusion Filter for Salvaged Blood CAK Microfilter, blood transfusion 2 LipiGuard SB
46 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
47 10887691000536 PXL8C PXL 8 High Efficiency Leukocyte Reduction Filter for Platelets with Attached Extension Set CAK Microfilter, blood transfusion 2 PXL 8
48 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
49 10812747018074 07-016 PLATELETMAPPING ASSAY AA JOZ SYSTEM, AUTOMATED PLATELET AGGREGATION 2 TEG HEMOSTASIS SYSTEM
50 10812747018067 07-015 PLATELETMAPPING ASSAY ADP 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 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
11 20812747018132 6211 DISPOSABLE CUPS & PINS, CLEAR TEG5000 HEMOSTASIS SYSTEM HAEMONETICS CORPORATION
12 20812747018033 07-008 LEVEL II CONTROL TEG5000 HEMOSTASIS SYSTEM HAEMONETICS CORPORATION
13 20812747018026 07-007 LEVEL I CONTROL TEG5000 HEMOSTASIS SYSTEM HAEMONETICS CORPORATION
14 20812747018019 07-006 DISPOSABLE CUPS & PINS HEPARINASE TEG5000 HEMOSTASIS SYSTEM HAEMONETICS CORPORATION
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.
20 20613994417286 402-02 CARTRIDGE 402-02 ACT RACT 13 LAN RACT MEDTRONIC, INC.
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
27 10812747018210 07-045 VALIDATION KIT, TEG5000 TEG5000 HAEMONETICS CORPORATION
28 10812747018203 07-044 STARTER KIT, TEG5000 TEG5000 HAEMONETICS CORPORATION
29 10812747018159 01-097 PIPETTE KIT, 1000UL TEG5000 HAEMONETICS CORPORATION
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.
43 10711234520055 HRS.110-L HRS.110-L Hemochron Whole Blood Coagulation System - Hemochron Response Instrument (Loaner) Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
44 10711234520048 HRS.RF HRS.RF Hemochron Whole Blood Coagulation System - Hemochron Response Instrument Refurbished Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
45 10711234520017 HRS.110 HRS.110 Hemochron Whole Blood Coagulation System - Hemochron Response Instrument Hemochron Whole Blood Coagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
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.
48 10711234510070 ELITEL ELITEL Hemochron Whole Blood Microcoagulation System - Hemochron Signature Elite Instru Hemochron Whole Blood Microcoagulation System - Hemochron Signature Elite Instrument (Loaner) Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
49 10711234510056 ELITEDEMO ELITEDEMO Hemochron Whole Blood Microcoagulation System - Hemochron Signature Elite Instru Hemochron Whole Blood Microcoagulation System - Hemochron Signature Elite Instrument (Demonstration) Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.
50 10711234510025 ELITERF ELITERF Hemochron Whole Blood Microcoagulation System - Hemochron Signature Elite Instru Hemochron Whole Blood Microcoagulation System - Hemochron Signature Elite Instrument Refurbished Hemochron Whole Blood Microcoagulation System ACCRIVA DIAGNOSTICS HOLDINGS, INC.