Other products from "HELENA LABORATORIES CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M52592330 9233 CFF IMMUNOELECTROPHORETIC, IMMUNOGLOBULINS, (G, A, M) 2 Antiserum to Human Serum
2 M52590150 9015 JZR SUPPORT GELS 1 IEP Sponge Wicks (2/pkg)
3 M52558520 5852 JOZ SYSTEM, AUTOMATED PLATELET AGGREGATION 2 Plateletworks Combo-25 Kit
4 M5255526140 552614 JHO ELECTROPHORETIC SEPARATION, LIPOPROTEINS 1 SPIFE Vis Cholesterol Kit
5 M5255527030 552703 CFF Immunoelectrophoretic, Immunoglobulins, (G, A, M) 2 SPIFE Nexus IFE-6 Antisera Kit
6 M525AQCHP0 AQC-HP JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 Actalyke QC Kit - AQC-HP
7 M52552920 5292 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 Protein S ELISA Kit
8 M52551280 5128 GKA ABNORMAL HEMOGLOBIN QUANTITATION 2 Hemolysate Reagent
9 M52590140 9014 JJN APPARATUS, ELECTROPHORESIS, FOR CLINICAL USE 1 Zip Zone Sponge Wicks
10 M5258JF520010 8JF52001 JPA SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES 2 AggRAM Module (Domestic)
11 M52563000000 6300000 LXG EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE 1 Pipette, Variable Volume, 10-100 microliter
12 M52557700040 5770004 JBP ACTIVATED WHOLE BLOOD CLOTTING TIME 2 Actalyke XL, (CSA/CE), W/ Flash Memory
13 M52556510 5651 KHE REAGENT, OCCULT BLOOD 2 ColoCARE Office Pack
14 M52518200 1820 CFF Immunoelectrophoretic, Immunoglobulins, (G, A, M) 2 V8 WASTE DRAWER PACK
15 M52592500 9250 CFF IMMUNOELECTROPHORETIC, IMMUNOGLOBULINS, (G, A, M) 2 Antiserum to Human IgE
16 M5255526040 552604 CIN ELECTROPHORETIC SEPARATION, ALKALINE PHOSPHATASE ISOENZYMES 2 SPIFE Alkaline Phosphatase Gel Kit
17 M5255525970 552597 CFF IMMUNOELECTROPHORETIC, IMMUNOGLOBULINS, (G, A, M) 2 Blade Applicator Kit, 12 Sample
18 M5255524710 552471 CEF ELECTROPHORETIC, PROTEIN FRACTIONATION 1 SPIFE SPE HI RES 20 KIT
19 M5255524570 552457 CFF IMMUNOELECTROPHORETIC, IMMUNOGLOBULINS, (G, A, M) 2 SPIFE IgG IEF-10 Kit
20 M5255523040 552304 CEF ELECTROPHORETIC, PROTEIN FRACTIONATION 1 QUICKGEL SPE Gel Kit
21 M5255522890 552289 CFF IMMUNOELECTROPHORETIC, IMMUNOGLOBULINS, (G, A, M) 2 SPIFE ULTRA IFE-6 ANTISERA KIT
22 M5255521640 552164 CFF IMMUNOELECTROPHORETIC, IMMUNOGLOBULINS, (G, A, M) 2 SPIFE Ultra ImmunoFix-9 Antisera Kit
23 M5255521360 552136 CEF ELECTROPHORETIC, PROTEIN FRACTIONATION 1 QUICKGEL MODIFIED APPLICATOR BLADES AND DEEP WELL CUPS
24 M5255521250 552125 CFF IMMUNOELECTROPHORETIC, IMMUNOGLOBULINS, (G, A, M) 2 SPIFE Ultra ImmunoFix-15 Antisera Kit
25 M5255519410 551941 JHO ELECTROPHORETIC SEPARATION, LIPOPROTEINS 1 SPIFE Vis Cholesterol Reagent Kit
26 M52553680 5368 GHR REAGENT, PLATELET AGGREGATION 2 Collagen Reagent
27 M52553600 5360 GGP TEST, QUALITATIVE AND QUANTITATIVE FACTOR DEFICIENCY 2 Rocket Stain
28 M52553410 5341 JPD HEMOGLOBIN A2 QUANTITATION 2 Beta-Thal HbA2 Quik Column Kit
29 M52553390 5339 JCM CONTROL, HEMOGLOBIN, ABNORMAL 2 Normal HbA2 Quik Column Control
30 M52551340 5134 JJT ENZYME CONTROLS (ASSAYED AND UNASSAYED) 1 CK/LD Isoenzyme Control (5 x 2 mL)
31 M52551270 5127 GKA ABNORMAL HEMOGLOBIN QUANTITATION 2 Hemolysate Reagent
32 M52551250 5125 GKA ABNORMAL HEMOGLOBIN QUANTITATION 2 Hemolysate Reagent
33 M52551020 5102 CIN ELECTROPHORETIC SEPARATION, ALKALINE PHOSPHATASE ISOENZYMES 2 Alkaline Phosphatase Indolyl Blue Reagent Kit
34 M52550930 5093 LXG EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE 1 Bufferizer
35 M52550900 5090 LXG EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE 1 Zip Zone Prep (1 x 60 mL)
36 M52550850 5085 KHE REAGENT, OCCULT BLOOD 2 ColoScreen-ES Take Home Pack
37 M52550830 5083 KHE REAGENT, OCCULT BLOOD 2 ColoScreen III 1000 Slide Pack
38 M52550820 5082 KHE REAGENT, OCCULT BLOOD 2 ColoScreen III Lab Pack
39 M52550050 5005 KEM AGENT, CLEARING 1 Clear Aid
40 M5255000910 500091 KHE REAGENT, OCCULT BLOOD ColoScreen Developer
41 M52540840 4084 JQW STATION, PIPETTING AND DILUTING, FOR CLINICAL USE 1 Super Z Applicator (8-sample)
42 M52536150 3615 GJG Pipette, Quantitative, Hematology 1 H-Pette II (No Blade, Metal Canula) (1000 pieces)
43 M52536120 3612 GJG Pipette, Quantitative, Hematology 1 H-Pette with Blade (1000 pieces)
44 M52534270 3427 LXG EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE 1 SPIFE Urine/CSF Protein Accessories (50 templates plus blotters)
45 M52534260 3426 JBD SYSTEM, ANALYSIS, ELECTROPHORETIC HEMOGLOBIN 2 QuickGel Accessory Kit
46 M52534250 3425 JJY Multi-analyte controls, all kinds (assayed) 1 SPE Abnormal Control (10 x 2 mL)
47 M52530580 3058 CIN ELECTROPHORETIC SEPARATION, ALKALINE PHOSPHATASE ISOENZYMES 2 TITAN GEL Alkaline Phosphatase Kit
48 M52530410 3041 CEF ELECTROPHORETIC, PROTEIN FRACTIONATION 1 TITAN GEL Serum Protein Kit
49 M52530240 3024 CEF ELECTROPHORETIC, PROTEIN FRACTIONATION 1 Titan III Cellulose Acetate (94 x 76 mm)
50 M52523190 2319 LXG EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE 1 SPIFE 4000 Applicator Blades
Other products with the same Product Code "JPA"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 03607450590272 59027 STA R Max® (with cap piercing option) DIAGNOSTICA STAGO
2 03607450590265 59026 STA R Max® DIAGNOSTICA STAGO
3 03607450590135 59013 STA R Max® DIAGNOSTICA STAGO
4 03607450590104 59010 STA R Max® (with cap piercing option) DIAGNOSTICA STAGO
5 03607450589900 58990 STA Compact Max® DIAGNOSTICA STAGO
6 03607450589894 58989 STA Compact Max® (with cap piercing option) DIAGNOSTICA STAGO
7 03607450589795 58979 STA-R Evolution® Expert Series (with cap piercing option) DIAGNOSTICA STAGO
8 03607450589788 58978 STA-R Evolution® Expert Series DIAGNOSTICA STAGO
9 03607450581041 58104 STA Satellite® DIAGNOSTICA STAGO
10 00842768026812 10487098 ORKL19 Standard Human Plasma for the calibration of coagulation and fibrinolysis tests Standard Human Plasma SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
11 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
12 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
13 00842768014222 10446232 ORHO37 Supplementary Reagent for coagulation tests Calcium Chloride Solution SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
14 00842768012358 10446541 OVMN11 The cuvettes serve coagulation tests as a reaction vessel. Cuvettes for BFT // Analyzer SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
15 00842768012259 10446530 OVKG03 The cuvettes serve coagulation tests as a reaction vessel. BFT II Analyzer Dispo System SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
16 00842768006869 10445989 OPCC03 For calibration of the Berichrom Heparin assay for measurement of unfractionated heparin Berichrom® Heparin UF Calibrator SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
17 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
18 00817869020311 SC-125, SC-126, H2O Hemotec Whole Blood Control Kit Large ANALYTICAL CONTROL SYSTEMS INC
19 00817869020274 SC-127 SC-127 Whole Blood Control Level III ANALYTICAL CONTROL SYSTEMS INC
20 00817869020267 SC-126 SC-126 Whole Blood Control Level II ANALYTICAL CONTROL SYSTEMS INC
21 00817869020250 SC-125 SC-125 Whole Blood Control Level I ANALYTICAL CONTROL SYSTEMS INC
22 00817869020007 CR-109 CR-109 .02M Calcium Chloride ANALYTICAL CONTROL SYSTEMS INC
23 00673978519173 550-90 CONTROL TEST 550-90 PROFICIENCY 5L NA MEDTRONIC, INC.
24 00613994615633 313-51 DEVICE 313-51 HEPTRAC ELEC QLT CNTRL CEM HEPtrac® MEDTRONIC, INC.
25 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.
26 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.
27 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.
28 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.
29 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.
30 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.
31 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.
32 B55880004001 800-0400 800-0400 The kACT Kit is an in vitro diagnostic test for use with the Sonoclot Coagulatio The kACT Kit is an in vitro diagnostic test for use with the Sonoclot Coagulation & Platelet Function Analyzer System. The kACT test is a kaolin activated whole blood clotting time test. It may also be used with citrated whole blood and plasma.The kACT kit is intended for high dose heparin management with or without aprotinin. The kACT test provides quantitative Onset/ACT and Clot Rate results with the Sonoclot Analyzer. The kACT test is not intended for platelet function monitoring.Each kACT Kit contains 100 lidded blue plastic activation cuvettes, 100 probes, and instructions for use. The activation cuvettes contain a controlled amount of kaolin and a magnetic stir bar. Sonoclot® kACT Kit SIENCO, INC.
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