Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human serum/plasma/control Specimen volume : 50 Microliter stored at 4 - 30 DegreeC Cat No : CFPC-89 INTENDED USE : ichroma AMH is a fluorescence Immunoassay (FIA) for the quantitative determination of AMH (Anti-m�¼llerian hormone) in human serum/plasma. It is useful as an aid in management and monitoring of premature ovarian insufficiency, menopause and ovarian reserve.For in vitro diagnostic use only. COMPONENTS : ichroma AMH consists of cartridges, detectors and diluent The cartridge contains the membrane called a test strip which has streptavidin at the test line and chicken IgY at the control line. All cartridges are individually sealed in an aluminum foil pouch containing a desiccant in a box The detector has 2 granules containing anti human AMH-fluorescence conjugate, anti-chicken IgY-fluorescence conjugate, anti-human AMH-biotin conjugate, bovine serum albumin (BSA) and sucrose as a stabilizer, MAB33 as a blocker in Tris-HCl buffer. All detectors are packed in a box The diluent contains bovine serum albumin and NaCl as a stabilizer, tween 20 and CA-630 as a surfactant and sodium azide as a preservative in phosphate buffered saline (PBS), and it is pre-dispensed in a vial. The diluent is packed in a box. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip.More antigens in sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show human AMH concentration in the sample. INTERPRETATION OF TEST RESULT : The instrument for ichroma tests calculates the test result automatically and displays AMH concentration of the test sample in terms of ng/mL The working range: 0.02- 15 ng/mL
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 30 Microliter Sample : human serum / plasma / control Reaction Time ; 10 mins Cat No : CFPC-32 Ferritin Monitoring deficiency/excess of iron & inflammation Ferritin is a universal intracellular protein that stores iron and releases it in a controlled fashion. Too little ferritin can lead to anemia, while too much to liver disease, rheumatoid arthritis, other inflammatory conditions, or hyperthyroidism. The ferritin test measures the level of ferritin in the blood. INTENDED USE : ichromaâ?¢ Ferritin is a fluorescence Immunoassay (FIA) for the quantitative determination of Ferritin in human serum/plasma. It is useful as an aid for quantifying human ferritin. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigen in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by Instrument for ichrom tests to show ferritin concentration in sample. MATERIALS SUPPLIED : REF CFPC-32 Components of ichroma Ferritin Cartridge Box: - Cartridge 25 - Detector 25 - Detector Diluent 1 - ID Chip 1 - Instruction for Use 1
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample : whole blood (AFIAS), plasma, serum Reaction Time : 15mins Detection Range : ichroma(TM) (1 - 100 mIU/ml) Cat No : CEPC-35 Follicle-stimulating Hormone (FSH) Diagnosis of early menopause & ovarian degeneration and infertility This test can help figure out the cause of infertility, problems with ovarian functions, menstrual abnormalities and congenital or acquired gonadotropin development disorder or infertility.
Product Details: Brand: Boditech Med Incorporated Size : 25 T Samples : human whole blood/serum/plasma Specimen volume ; 150 microliter stored at 4-30 DegreeC Cat No : CFPC-23-1 PCT Assessing initial risk of bacterial infection and fatal sepsis Diagnosis of sepsis is routinely performed in intensive care units (ICU) of all hospitals. Early detection of sepsis is very important in determining appropriate treatment as it is known to improve patient survival through a various therapeutic strategy for sepsis. The ichroma & AFIAS PCT test helps detect bacterial sepsis and assess the risk of developing septic shock. INTENDED USE : ichroma PCT is a fluorescence Immunoassay (FIA) for the quantitative determination of Procalcitonin (PCT) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of bacterial infection and sepsis. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PCT concentration in sample. STORAGE AND STABILITY: The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately. MATERIALS SUPPLIED : REF CFPC-23 Components of ichromaâ?¢ PCT Cartridge Box: - Cartridges 10 - ID Chip 1 - Instruction For Use 1 Box containing Detection Buffer tubes - Detection Buffer Tubes 10
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 75 Microliter Sample : human serum/plasma Reaction Time : 15mins Cat No : 13010 Luteinizing Hormone (LH) Assessing and monitoring function of pituitary gland This test helps evaluate pituitary function by quantifying luteinizing hormone in the blood, to diagnose pituitary gland disease, and to determine congenitally or acquired gonadotropin dysfunction. INTENDED USE : ichroma LH is a fluorescence Immunoassay (FIA) for the quantitative determination of Luteinizing hormone (LH) in human serum/plasma. It is useful as an aid in management and monitoring of determination of evaluating fertility issues, function of reproductive organs (ovaries or testicles), or detection of the ovulation. For in vitro diagnostic use only. PRINCIPLE: The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show LH concentration in sample. MATERIALS SUPPLIED: REF 13010 Components of ichroma LH Cartridge Box: - Cartridges 25 - ID Chip 1 - Instruction For Use 1 Box containing Detection Buffer Tubes - Detection Buffer Tubes 25.
Product Details: Number of Reactions(Preps)/Kit 30 Brand : CTK BioTech Result Time (Rapid Kits) :20-25 Min Sample Material :Serum / Plasma / Whole Blood Cat. No : R0061c The OnSite Dengue IgG/IgM 3.0 Combo Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM antiâ??dengue virus (DEN1, 2, 3 and 4) in human serum, plasma or whole blood. Product Features: Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes IgM detection indicates recent infection IgG detection indicates recent or previous infections Each kit contains: Individually sealed foil pouches containing: One cassette device One desiccant 5 AUL Capillary tubes Sample diluent (REF SB-R0061, 5 mL/bottle) One package insert (instruction for use)
Product Details: Brand : Boditech Med Incorporated Size : 25 T Specimen : human serum/plasma Specimen volume : 50 Microliter Cat. No. : CFPC-47 INTENDED USE : ichromaâ?¢ Vitamin D is a fluorescence Immunoassay (FIA) for the quantitative determination of total 25(OH)D2/D3 level in human serum/plasma. It is useful as an aid in management and monitoring of regulating the concentration of calcium and phosphate in the bloodstream and promoting the healthy growth and remodeling of bone.For in vitro diagnostic use only. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of 25(OH)D3 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal. STORAGE AND STABILITY : The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. The releasing buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. Opened detection buffer and releasing buffer are stable for 12 months at 2-8 C if kept capped in original container and free from contaminations. After the cartridge pouch is opened, the test should be performed immediately. MATERIALS SUPPLIED : REF CFPC-47Components of ichroma Vitamin D Cartridge Box:- Cartridges 25- Sample Mixing Tubes 25- ID Chip 1- Instruction For Use 1 Detection Buffer Vial (3 mL) 1 Releasing Buffer Vial (2 mL) 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human whole blood/serum/ plasma Sample volume : 50 Microliter stored at 4 - 30 DegreeC Cat No : CFPC-65 Troponin I (Tn-I) Plus Early diagnosis of myocardial infarction with high sensitivity Troponin I (Tn-I) Plus can diagnose myocardial infarction and myocardial necrosis at an early stage with high sensitivity by accessing Tn-I level in the blood, thus can help prevent progression to more severe cases. INTENDED USE: ichroma Tn-I Plus is a Fluorescence Immunoassay (FIA) for the quantitative determination of cardiac troponin-I (Tn-I) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of acute myocardial infarction (AMI). For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show Tn-I concentration in the sample. MATERIALS SUPPLIED : REF CFPC-65 Components of ichroma Tn-I Plus Cartridge Box: - Cartridge 25 - 50L Capillary tube 25 - ID chip 1 - Instruction for Use 1 Buffer Box For ichorma II - Detector (Capped with plastic lid) 25 - Diluent 1 For ichroma 50 - Detector (Sealed with aluminum foil) 25 - Diluent 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human whole blood/ serum/ plasma/control Specimen volume : 10 Microliter stored at 4 - 30 DegreeC Cat No : CFPC-77 NT-proBNP Helping to diagnose heart diseases and evaluate the severity level BNP and NTproBNP are peptides that are continuously produced in the heart. When the muscles in the left ventricle over-stretch as in heart failure, the secretion of these peptides into blood increases. One may utilize the level of NTproBNP in blood to assess the cardiac event and its severity. Both of BNP and NTproBNP can be used to show different aspects of the heart failure. INTENDED USE: ichroma NT-proBNP is a fluorescence Immunoassay (FIA) for the quantitative determination of NT-proBNP in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of persons suspected of having congestive heart failure. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto the nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show NT-proBNP concentration in the sample. MATERIALS SUPPLIED : REF CFPC-77 Components of ichroma NT-proBNP Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 Buffer Box For ichroma - Detector tube 25 - Detector diluent 1 For ichromaâ?¢-50 - Detector tube 25 - Detector diluent 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : human whole blood/serum/plasma Specimen volume : 5 Microliter stored at 4-30 C Cat No : CFPC-51 Anti-CCP Plus Supporting to distinguish and diagnose rheumatoid arthritis This test helps to diagnose and provide appropriate treatment for chronic systemic autoimmune diseases and rheumatism by quantifying Anti-CCP in the blood. INTENDED USE : ichroma Anti-CCP is a fluorescence Immunoassay (FIA) for the qualitative or semi-quantitative determination of human IgG autoantibodies to cyclic citrullinated peptides (CCP) in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of rheumatoid arthritis (RA) in combination with other clinical and laboratory findings. For in vitro diagnostic use only. STORAGE AND STABILITY : The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately. PRINCIPLE : A synthetic cyclic citrullinated peptide (CCP) is immobilized on a porous membrane. After a sample is added to the sample port, detection buffer, consisting of fluorescent conjugated polyclonal antibody to human IgG, is loaded to the buffer port. The more anti-CCP antibodies in sample forms the more the peptide antigen/anti-CCP antibodies complex and leads to stronger intensity of fluorescence signal on detector anti-human IgG, which is processed by instrument for ichroma tests to show anti-CCP level in sample. MATERIALS SUPPLIED : REF CFPC-51 Components of ichroma Anti-CCP Cartridge Box: - Cartridges 25 - Sample collectors 25 - ID Chip 1 - Instruction For Use 1 Box containing Detection Buffer Tubes - Detection Buffer Tubes 25
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples: human whole blood/serum/ plasma Specimen volume : 50 microliter stored at 4 - 30 C Cat No : CFPC-91 Total IgE Assessing to diagnose acute allergic diseases This test assesses IgE in blood to support diagnosing of acute allergic diseases. INTENDED USE : ichroma Total IgE is a fluorescence immunoassay (FIA) for the quantitative determination of total IgE in human whole blood/serum/ plasma. It is useful as an aid in diagnosis and management of allergic disease. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show total IgE concentration in the sample. MATERIALS SUPPLIED : REF CFPC-91 Components of ichroma Total IgE Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 Detection Buffer Box - Detection Buffer 25
Product Details: Brand : Boditech Med Incorporated Size ; : 25 T Samples : Human whole blood/plasma/control Specimen volume : 10 Microliter Storage : 4- 30 DegreeC Cat No : CFPC-25 D-Dimer Measuring D-dimer level in 12 mins The presence of D-dimer in blood indicates that thrombin has been formed and fibrin generated from fibrinogen in vivo as a result of activation of the coagulation system. This test measures the level in the blood to help assess the thrombotic state. INTENDED USE : ichroma D-Dimer is a fluorescence Immunoassay (FIA) for the quantitative determination of D-Dimer in human whole blood/plasma. It is useful as an aid in management and monitoring of post therapeutic evaluation of thromboembolic disease patients. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show D-Dimer concentration in the sample. MATERIALS SUPPLIED : REF CFPC-25 Components of ichroma D-Dimer Cartridge Box: - Cartridge 25 - ID chip 1 - Instruction for use 1 Box containing Detection Buffer tubes - Detection buffer 25
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 75 Microliter Sample : serum/plasma/control Storage Temperature : 4-30 DegreeC. Cat No : CFPC-27 Prolactin (PRL) Assessing to diagnose hypothalamic impairments & pituitary disorders This test helps select and diagnose mammary gland development, infertility treatment and pituitary diseases by quantifying blood PRL. INTENDED USE : ichroma PRL is a fluorescence Immunoassay (FIA) for the quantitative determination of Prolactin (PRL) in human serum/plasma. It is useful as an aid in management and monitoring of hypothalamic-pituitary disorders. For in vitro diagnostic use only. PRINCIPLE: The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigenantibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PRL concentration in sample. MATERIALS SUPPLIEED : REF CFPC-27 Components of ichroma PRL Cartridge Box: - Cartridges 25 - ID Chip 1 - Instruction for Use 1 Detection Buffer Box: - Detection Buffer tubes 25
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 10 Microliter Sample : Human whole blood/serum/ plasma/control Reaction Time : 3 mins Cat No : ichroma CRP-25 CRP Assessing to diagnose infection and inflammation This test can help with proper prescription and treatment by quickly and accurately measuring CRP with a finger-tip blood. INTENDED USE : ichroma CRP is a fluorescence Immunoassay (FIA) for the quantitative determination of CRP in human whole blood/serum/ plasma. It is useful as an aid in management and monitoring of autoimmune diseases and infectious processes, such as rheumatoid arthritis. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show CRP concentration in the sample. MATERIALS SUPPLIED : REF i-CHROMA CRP-25 Components of ichrom CRP Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 - Sample Collector 25 Box containing Detection Buffer - Detection buffer 25
Product Details: Number of Reactions(Preps)/Kit 30 T Brand SD Biosensor ICMR Approved Yes Result Time (Rapid Kits) 10 Min Cat. No RK033-30 General Description: STANDARD Q HIV/Syphilis Combo Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies specific to HIV-1 including subtype O, HIV 2 and Syphilis (Treponema pallidum) in human serum, plasma or whole blood. The test is for in vitro diagnostic use and intended as an aid to early diagnosis of HIV and Syphilis infection for HIV or Syphilis infected patients, patients with signs and symptoms (HIV and Syphilis) and persons at risk. The test is able to quick screen the HIV/syphilis infection and gives the advantage of managing these two diseases at the same time. Technical specifications: Technology: Rapid chromatographic immunoassay. Format: Test cassette, 25 tests. Sample type: serum/plasma/venous whole blood specimen Sample volume: Serum Plasma 10�µl/whole Blood 20 µl. Sensitivity: HIV 100% & Syphilis 98.8% Specificity: HIV 99.9%/syphilis 100%/ Time to result: Minimum of 15 minutes.
Product Details: Number of Reactions(Preps)/Kit 25 Test Brand SD Biosensor Result Time (Rapid Kits) 15 Min Cat. No 09LEP10D STANDARD Q Leptospira IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Leptospira interrogans in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity. Advantage Differential detection of IgG and IgM antibodies Easy to use, Easy to read and interpret Room temperature storage of 2-40 / 36-104 Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl).
Product Details: Brand J.Mithra Test Kit Type: Dengue Test Kit (Rapid) Sensitivity & Specificity High Shelf Life: 30 months at 2-30 DegreeC Pack Size: 10, 30 & 50 Tests Cat. No IR028010 Intended Use : Dengue Day 1 Test is a rapid solid phase immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen and differential detection of IgM and IgG antibodies to Dengue virus in Human serum/plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue infection & presumptive diagnosis between primary and secondary Dengue infection. Salient Features: First line testing kit for detecting dengue infection from day 1 using NS1 Antigen & differential detection of IgM & IgG Antibodies. Diagnosis of both Primary & Secondary Infection. Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4). Highly Sensitive & Highly Specific Long shelf life: 30 months at 2-30 C. Convenient pack sizes: 10 Tests, 30 Tests & 50 Tests. Principle:Dengue Day 1 test kit consists of two devices: one device for detection of Dengue NS1 antigen and second device for the differential detection of Dengue IgM/IgG antibodies in Human serum/plasma. Dengue NS1 Antigen device contains two lines; (Control line) & T (Dengue NS1 Antigen test line). Test line is coated with anti-dengue NS1 Ag. When a sample is added to the device, Dengue NS1 antigen if present in the sample will bind to the anti-dengue NS1 gold colloidal conjugate making antigen antibodies complex. This complex migrates along the membrane to the test region and forms the visible pink line at as antibody-antigen-antibody gold colloid forms. Dengue IgM/IgG test device contains three lines; C (Control line), M (IgM test line) & G (IgG test line).IgM test line is coated with anti-human IgM and IgG test line is coated with anti-human IgG.When a sample is added to the device, IgG and IgM antibodies in the sample react with anti-human IgM or IgG antibodies coated on the membrane respectively. Colloidal gold complexes containing dengue 1-4 antigens is captured by the bound anti-dengue IgM or IgG on respective test bands located in the test window causing a pale to dark red band to form at the IgG or IgM region of the test device window. The intensity of the test bands in the respective device will vary depending upon the amount of antigen /antibody present in the sample. The appearance of any pink/ red colour in a specific test region should be considered as positive for that particular antigen and/or antibody type (IgG or IgM). A red procedural control line should always develop in the test device window to indicate that the test has been performed properly Dengue NS1 Ag : Sensitivity 96% and Specificity 98%. Dengue IgM/IgG Antibody test : Sensitivity 95% and Specificity 97%.
Product Details: Brand J.Mithra Result Time (Rapid Kits) Within 20 Minutes Test Kit Type Malaria Test Kit (Rapid) Sensitivity & Specificity Excellent as per WHO Malaria RDTs Evaluation Cat. No IR221050 Intended Use:Advantage MAL Card is a visual, rapid and sensitive immunoassay for the qualitative diagnosis of P.falciparum and other Plasmodium Species (P.vivax/ P.malariae/ P.ovale/ P.falciparum) based on pLDH antigen in human whole blood. Salient Features: Infection free- See through Device based on pLDH antigen Malaria parasite in whole blood Excellent Sensitivity & Specificity as per WHO Malaria RDTs Evaluation. Longer shelf life of 30 months at 4-30 C. Easy to interpret Colour Bands Results within 20 minutes.
Product Details: Brand J.Mithra Result Time (Rapid Kits) Within 3 Minutes Test Kit Type HCV Test Kit (Rapid) Sensitivity 100% WHO Evaluation Specificity 98.9% WHO Evaluation Cat. No HC020100 Intended Use: The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C virus in human serum or plasma. It has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigen Salient Features: Based on Flow Through Technology, which is similar to Elisa technology because of involvement of washing steps at various levels to enhance the specificity. Use of highly purified HCV antigens for Core, NS3, NS4, NS5 immobilized on the device. Detection of all the subtypes of HCV. Results within 3 minutes. In built quality control dot which validates the test. 100% Sensitivity & 98.9% Specificity as per WHO evaluation. Shelf life : 24 months at 2-8C
Product Details: Brand Abbott Afinion Result Time (Rapid Kits) 15 min Sample Type Blood Country of Origin Made in India Requires only 20 ml of specimen Capillary tubes 20 ml Immediate point of care HbA1c results for efficient monitoring of glycemic control. The Afinion HbA1c assay is a test for quantitative determination of glycated hemoglobin (HbA1c) in human whole blood, used to monitor metabolic control in patients with diabetes. It provides the immediate test results you need for improved diabetic control, better patient outcomes, and enhanced clinic efficiencies. SHORT ASSAY TIME IN 3 MINUTES The CLIA-Waived Afinion HbA1c test gives you reliable, high quality results conveniently available when and where you need them. TIMELY TREATMENT CHANGES Diabetes can be treated and managed by healthful eating, regular physical activity, and medications to lower blood glucose levels. Lowering the HbA1c has been shown to reduce microvascular complications of diabetes and is also associated with long-term reduction in macrovascular disease. LONG SHELF LIFE OF REAGENTS Patient consultations can be carried out with confidence. The HbA1c Test Cartridge contains all reagents necessary for the measurement of glycated hemoglobin. The test has 3 months room temperature storage.
