Product Details: Number of Reactions(Preps)/Kit : 10T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15 min CAT No : RK013-10 One step, rapid, immunochromatographic test for the detection of IgM/IgG antibodies to four serotypes of dengue virus (DEN-1, DEN-2, DEN-3 and DEN-4) & Dengue virus NS1 antigen in human serum, plasma or whole blood. Kit Contents: Standard Q Dengue Ag Ab Duo cassette x 10 Specimen transfer device 10ml x 10 Butter bottle 4ml x 01 Instructions for use x 1 STANDARD Q Dengue Duo test is an immunochromatographic assay for the detection of NS1 antigen and Dengue virus-specific IgM and IgG antibodies in human serum, plasma and whole blood. By detecting the NS1 antigen, not only the initial infection can be detected, but also Dengue virus-specific IgM and IgG can be detected at the same time. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.
Product Details: Number of Reactions(Preps)/Kit :20T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15min CAT No : RK012-20 One step, rapid, immunochromatographic test for the detection of Dengue IgMlIgG antibodies to four senatypes of dengue virus (DEN-I, DEN-2. DEN-3 and DEN-4) in human serum, plasma or whole blood. Kit Contents: Standard Q Dengue IgM IgG cassette x 20 Specimen transfer device 10ml x 20 Butter bottle 4ml x 01 Instructions for use x 1 STANDARD Q Dengue IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting IgM and IgG specific to Dengue virus, the primary and secondary Dengue virus infections can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity. Advantage: Differential detection of IgG and IgM antibodies Easy to use, Easy to read and interpret Room temperature storage Able to read positive/negative infections fast and accurately with a little amount of sample (10 �µl)
Product Details: Number of Reactions(Preps)/Kit 40T Brand ; SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15min CAT No : RK025-40 One step, rapid immunothematographic test for the differential detection between Plasmodium falciparum Histidine- Rich Protein II (HRP II) and Plasmodium species (P. falciparum , P vivax P. ovale, P. malariae) lactate dehydrogenase (pLDH) in human whole blood Kit Contents: Standard Q Malaria Pf/PV Ag cassette x 40 Specimen transfer device 3 microlitre x 40 Butter bottle 3m1 x 02 Instructions for use x 01 STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity Advantage: Distinguish the infection between P.falciparum and P.vivax Optimized on-site diagnosis with the small diagnostic kit Able to read positive/negative infections fast and accurately with a little blood (5aul) Room temperature storage.
Product Details: Number of Reactions(Preps)/Kit : 40T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15 min CAT No : RK027-40 STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and Plasmodium species antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium species, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity. Distinguish the infection between P.falciparum and others Optimized on-site diagnosis with the small diagnostic kit Able to read positive/negative infections fast and accurately with a little blood (5aul) Room temperature storage
Product Details: Number of Reactions(Preps)/Kit: 30T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits): 10 min Country of Origin : Made in India CAT No : RK026-30 STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes. Easy to use, Easy to read and interpret Room temperature storage Performance Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
Product Details: Number of Reactions(Preps)/Kit : 20T Brand ; SD Biosensor ICMR Approved ; Yes Result Time (Rapid Kits) : 15 min CAT No : RK029-20 STANDARD Q TSUTSUGAMUSHI IgM/IgG is a rapid,sensitive,qualitative Immunochromatographic assay for the detection of IgM/IgG antibodies against Orientia Tsutsugamushi in human serum,Plasma or whole blood specimen.it is an initial screening test and this test kit is for in vitro use only by professionals. Differential detection of IgM & IgG Antibodies Easy to use,Easy to interpret Long term storage Faster results with lesser specimen volume (10aul)
Product Details: Number of Reactions(Preps)/Kit : 20T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15 min CAT No : RK024-20 STANDARD Q Chikungunya IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Chikungunya virus in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity. Differential detection of IgG and IgM antibodies Easy to use, Easy to read and interpret Room temperature storage Able to read positive/negative infections fast and accurately with a little amount of sample (10 aul)
Product Details: Number of Reactions(Preps)/Kit : 25T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15 min CAT No : 09FIL10D Filariasis Ag Test Kit Contents: Test Device in a foil pouch with desiccant Disposable dropper Instruction for use
Product Details: Number of Reactions(Preps)/Kit : 30T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15 min CAT No : RK018-30 STANDARD Q HCV Ab qualitatively analyzes antibodies specific to hepatitis C virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis C infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 5 minutes. Easy to use, Easy to read and interpret Room temperature storage Performance Sensitivity : 98.9% (92/93) / Specificity : 100% (168/168)
Product Details: Number of Reactions(Preps)/Kit : 50T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 10 min CAT No : RK022-50 "STANDARD QA Ultra-DotA HIV Test is a rapid, sensitive andqualitative immunochromatographic assay to detect circulatingantibodies against HIV in human serum or plasma. The test is for invitro diagnostic use and is intended as an aid to early diagnosis ofHIV infection. This test is intended for professional use only as aninitial screening test."
Product Details: Number of Reactions(Preps)/Kit : 50 Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 10 min CAT No : RK023-50 STANDARD QA Ultra-DotA HCV Test is a rapid, sensitive andqualitative immunochromatographic assay to detect antibodiesagainst HCV in human serum or plasma. This test is for in vitrodiagnostic use and intended as an aid to early diagnosis of HCVinfection in patient with clinical symptoms with HCV infection.The test provides an initial screening result only. More specificalternative diagnosis methods should be performed in order toobtain the confirmation of HCV infection.
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human serum/plasma/ control Specimen volume : 75 Microliter stored at ; 4 - 30 DegreeC Cat No ; CFPC-44 T3 Assessing to diagnosis & to monitor thyroid diseases(T3) This test assesses the level of T3 in the blood to diagnose thyroid dysfunction, help to receive appropriate treatment, and help to confirm the treatment effect through periodic measurement. INTENDED USE : ichroma T3 is a fluorescence Immunoassay (FIA) for the quantitative determination of triiodothyronine (total T3) in human serum/plasma. It is useful as an aid in management and monitoring of determination of thyroid disorders. For in vitro diagnostic use only. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) 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 T3 and bovine serum albumin (BSA) is immobilized and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal. MATERIALS SUPPLIED : REF CFPC-44 Components of ichroma T3 Cartridge Box: - Cartridge 25 - Detector tube 25 - Detector diluent 2 - ID chip 1 - Instruction for Use 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Specimen : Human serum/plasma/ control Specimen volume : 75 microliter stored at 4 - 30 DegreeC. Cat No : CFPC-26 T4 Assessing to diagnosis & to monitor thyroid diseases(T4) Thyroxine (T4) is a type of thyroid hormone. An abnormal amount of T4 may indicate thyroid disease. The T4 test measures total T4, including T4 bonded to protein and free T4. A T4 test will help determine what type of problem is affecting the thyroid. INTENDED USE : ichroma T4 is a fluorescence Immunoassay (FIA) for the quantitative determination of thyroxine (T4) in human serum/plasma. It is useful as an aid in management and monitoring of thyroid disorder. 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 detector, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T4 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. MATERIALS SUPPLIED : REF CFPC-26 Components of ichroma T4 Cartridge Box: - Cartridges 25 - ID Chip 1 - Insert 1 - Detector tube (Granule) 25 - Detector diluent (5.5 mL) 1
Product Details: Brand ; Boditech Med Incorporated Size : 25 T Samples: human whole blood/serum /plasma Specimen volume human whole blood/serum/ plasma stored at 4-30 C Cat. No. : CFPC-66 Human Chorionic Gonadotropin (�²-hCG) Distinguish pregnancy and abnormal pregnancy The IhCG test can be used to confirm pregnancy, the age of the fetus, abnormal pregnancy (ectopic pregnancy), potential miscarriage, and down syndrome. INTENDED USE : ichroma -HCG Plus is a fluorescence Immunoassay (FIA) for the quantitative determination of -HCG in human whole blood/serum /plasma. It is useful as an aid in management and monitoring of beta human chorionic gonadotropin (hCG) level in human For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; Dried antibodies in the detector tube, once diluted with the diluent, bind with antigens in the sample to form antigen-antibody complexes. These complexes then migrate through the nitrocellulose matrix and are captured by another sets of immobilized antibodies on the test line. The more antigens in the sample, the more antigen-antibody complexes, which leads to a stronger fluorescence signal. This signal then is interpreted by the reader to display the �²-HCG concentration in the sample. STORAGE AND STABILITY : The cartridge is stable for 20 months (while sealed in the original aluminum foil pouch) if stored at 4-30 C. The detector, diluent and sample diluent are 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-66 Components of ichroma-HCG Plus Cartridge Box: - Cartridges 25 - ID Chip 1 - Instruction For Use 1 Buffer Box For ichorma II - Detectors (Capped with plastic lid) 25 - Diluent 1 For AFIAS-50 - Detectors (Sealed with aluminum foil) 25 - Diluent 1 Sample Diluent Box: - Sample Diluent Tubes 25
Product Details: Brand: Boditech Med Incorporated Size : 25 T Samples : human serum/plasma Specimen volume : 150 Microliter stored at 4 - 30 DegreeC. Cat. No : CFPC-22 Thyroid Stimulating Hormone (TSH) Diagnosing thyroid dysfunction One needs an adequate level of thyroid hormone. The excessive or insufficient level would cause various abnormalities in human physiology. The TSH test can deliver the required answer about the hormone level in 12 minutes with fingertip blood (US FDA 510k; AFIAS TSH). 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 II - Detector tube 25 - Detector diluent 1 For ichroma-50 - Detector tube 25 - Detector diluent 1
Product Details: Brand : Boditech Med Incorporated Size : 25 Test Samples : Whole blood Sample volume : 75 Microliter Cat No : CFPC-38 Storage Temperature ; 4 - 30 DegreeC HbA1c Assessing the level of glycated hemoglobin in the blood This test is certified by NGSP (National Glycohemoglobin Standardization Program). It helps diabetic diagnosis, treatment, and prognosis by measuring the glycated hemoglobin concentration (%) in a small amount of blood over the past 3 months. INTENDED USE ichroma HbA1c is a fluorescence Immunoassay (FIA) for the quantitative determination of HbA1c(Hemoglobin A1c) in human whole blood. It is useful as an aid in management and monitoring of the longterm glycemic status in patients with diabetes mellitus. 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. Instrument for ichromaâ?¢ tests displays the content of glycated hemoglobin in terms of percent of the total hemoglobin in blood.
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : whole blood/serum/plasma Sample volume : 75 Microliter stored at 4 - 30 DegreeC Cat No i CHROMA PSA-25 Prostate Specific Antigen (PSA) Screening for the prostate cancer & monitoring the effects of the treatment This test helps in the early detection of prostate diseases such as enlarged prostate and prostatitis and prostate cancer by quantifying PSA in male blood, as well as observation of treatment effects and monitoring of recurrence.
Product Details: Brand ; Boditech Med Incorporated Size : 25 Test Samples : Serum/Plasma Recommended anticoagulant K2 EDTA, K3 EDTA, sodium heparin Storage Temperature : 4 - 30 DegreeC Cat No : CFPC-21 Progesterone Monitoring ovulation abnormalities and predicting miscarriage & ectopic pregnancy The progesterone test kit measures the level of progesterone in the blood. The progesterone test alone is not enough to diagnose a particular problem. But the result may help provide answers to causes of infertility, risk of miscarriage, ovulation, and ectopic pregnancy. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) 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 progesterone and bovine serum albumin (BSA) is immobilized, and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal.
Product Details: Number of Reactions(Preps)/Kit : 30T Brand : CTK BioTech Result Time (Rapid Kits) : 15 min Sample Type : Blood Test Type : Rapid Test CAT No : R0101C Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 �¼mol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 �¼mol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant 5L capillary tubes Sample diluent (REF SB-R0101, 5 mL/bottle) One package insert (instruction for use)
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
