Number of Reactions(Preps)/Kit : 10T
Brand : CTK BioTech
Result Time (Rapid Kits) : 10 min
Sample Type : Blood
Test Type : Rapid test
CAT No : R0063C
Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 auL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit : 10T
Brand : CTK BioTech
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : AR0151C
Use of conserved antigens allows pan-filaria tests to be applicable
Simple procedure provides alternative to diagnosis by blood smear
Use serum, plasma or whole blood
No restrictions on time of day for sample collection
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Plastic droppers
Sample diluent (1 bottle, 5 mL)
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit : 25T
Brand : CTK BioTech
Result Time (Rapid Kits) : 10 min
Sample Type : Blood
Test Type :Rapid Test
CAT No : R2011C
Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL
Higher accuracy, sensitivity and specificity than the Guaiac Test
No dietary restrictions
Clear, easy-to-interpret result
Individually sealed foil pouches containing:
One cassette test device
One desiccant
Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011)
Patient ID stickers
One package insert (instruction for use)
Product Details:
Number of Reactions(Preps)/Kit ; 25T
Brand : CTK BioTech
Result Time (Rapid Kits) : 10 min
Sample Type : Blood
Test Type : Rapid Test
CAT No : R0192C
Clinical accuracy: 96.7% sensitivity, 93.8% specificity
Analytical sensitivity: 100% positive detection rate at 1 ng/mL of pylori lysate antigen in fecal specimens
Cross reactivity: no cross reactivity with the following organisms at â?¥ 1 x 108 org/mL: Acinetobacter calcoaceticus, Neisseria gonorrheae, Adenovirus, Neisseria meningitides, Enterococcus faecalis, Proteus mirabilis, Escherichia coli, Proteus vulgaris Hauser, Gardnerella vaginalis, Pseudomonas aeruginosa, Geotrichum candidum, Rotavirus, Haemophilus influenza, Salmonella Paratyphi A, �±-haemolytics streptococcus, Salmonella Paratyphi B, �²-haemolytic streptococcus, Salmonella Paratyphi C, Klebsiella pneumonia, Salmonella typhi, Moraxella catarrhalis
Interference: No interference was seen with 5 mg/mL Tums�® Antacid, 1:20 Pepto-Bismol�® Antacid, 5 mg/mL Tagamet�® Antacid, 5% Barium sulfate, 5 mg/mL Prilosec Antacid, 12.5% Hemoglobin (tarry stool), or 1:20 Mylanta�® Antacid
Shelf life: 24 month
Individually sealed foil pouches containing:
One cassette device
One desiccant
Stool collection devices, each containing 2 mL extraction buffer
Plastic droppers for transferring watery stool
Package insert (instruction for use)
Number of Reactions(Preps)/Kit : 10
Brand : CTK BioTech
Result Time (Rapid Kits): 15 min
Sample Type : Blood
Test Type Rapid Test
CAT No : R0090C
Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 aUL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use)
1186 Rapid Test Kits Suppliers
Short on time? Let Rapid Test Kits sellers contact you.
Product Details:
Number of Reactions(Preps)/Kit : 25
Brand : CTK BioTech
Result Time (Rapid Kits) ; 15 min
Sample Type : Blood
Test Type Rapid Test
CAT No : R0162C
Detects the specific antigens from either S. typhi or S. paratyphi
Earlier detection results in faster treatment for disease eradication
Works with a variety of specimen types including: fecal, blood culture
Simple procedure minimizes operator error due to sample preparation
Test result within 15 minutes allows medical professionals to take immediate action
High level of reproducibility
Test kits can be used and stored at room temperature
Individually sealed foil pouches containing:
One cassette device
One desiccant
Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer (REF SB-R0162)
Sample diluent (REF SB-R0162-2, 5 mL/bottle)
Plastic droppers
Patient ID stickers
One package insert (instruction for use).
Product Details:
Number of Reactions(Preps)/Kit 10 T
Brand CTK BioTech
Test Type Rapid test
Sample human serum, plasma, or whole blood
Test time 10 Min
Cat No : R0253C
The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood.
This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.
Recommended for use:
Any person presenting with clinical signs or symptoms consistent with TORCH infection.
Women who are pregnant or who are planning to become pregnant
Individuals with a compromised immune system
The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection.
The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection.
The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2.
Product Specification :
Individually sealed foil pouches containing:
One cassette device
Two desiccants
Plastic droppers
Sample diluent (REF SB-R0253, 5 mL/bottle)
One package insert (instruction for use)
Number of Reactions(Preps)/Kit 30T
Brand CTK BioTech
ICMR Approved Yes
Result Time (Rapid Kits) 20min
CAT No : AR5001C
Details :
Utilizes Recombinant Orientia tsutsugamushi antigens.
Qualitative detection and differentiation of antibodies(IgG and IgM) against Orientia tsutsugamushi (Scrub typhus)
Compatible with Whole blood, Serum and Plasma.
Sensitivity: For IgG 95.4% and IgM 96.1%, Specificity: For IgG 96.8% and IgM 97.6%.
Results in 20 minutes.
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Detection buffer (tris-based buffered solution with preservatives)
Instructions for Use
Brand J.Mithra
Test Kit Type HBsAg Test Kit (Rapid)
Detects All the 11 subtype of HBsAg
Sensitivity 100% by WHO Evaluation
Specificity 100% by PATH USA Evaluation
Cat. No HB010100
Intended Use : Hepacard is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV).
Salient Features:
Detects all the 11 subtype of HBsAg.
Antigen Sensitivity- 0.5 ng/ml.
No sample preparation required.
See through Device for easy result interpretation.
Shelf life-30 months at 2-30C.
WHO Evaluated with 100% Sensitivity.
Evaluations:
PATH USA: Sensitivity 100% and Specificity 100% .
DEPT. OF CLINICAL VIROLOGY, CMC VELLORE: Sensitivity 100% and Specificity 100%
Approved By Drug Controller General Of India( DCGI) For use In Blood Banks.
Product Details:
Usage/Application Hospital
Test for quantitative determination of albumin, creatinine and albumin/creatinine ratio (ACR) in human urine, used for early identification of renal disease in patients with diabetes and/or hypertension.
BENEFITSTIMELY TREATMENT CHANGES
The Afinion ACR (albumin, creatinine and albumin/creatinine ratio) detects microalbuminuria in human urine. Microalbuminuria is the first clinical sign of diabetic renal disease and cardiovascular disease. Simple testing for microalbuminuria is extremely efficient as an early indicator of renal failure.
SHORT ASSAY TIME IN 5 MINUTES
The Afinion ACR test gives you reliable results conveniently available when and where you need them.
Patient consultations can be carried out with confidence. The Afinion ACR Test Cartridge contains all reagents necessary for the measurement of albumin, creatinine and albumin/creatinine ratio.
Number of Reactions(Preps)/Kit : 96 wells
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 1hr 40 mins
STANDARD E Dengue IgM ELISA analyzes IgM antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay.
Simple and easy to use - All necessary reagents included in the kit
Highest accuracy with all dengue serotypes(DEN1,2,3, and 4)
Performance
Sensitivity : 97.4% (77/79) / Specificity : 96.6% (346/358)
Product Details:
Number of Reactions(Preps)/Kit ; 2
Brand ; iHEALTH
Test Method : Antigen Test
Result Time (Rapid Kits) : 15mins
Sample Type : Nasal Swab
Cat. No : ICO-3000
iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
Product Details:
Brand : Abbott
ICMR Approved ; Yes
Sample Type : Nasal Swab
Packaging Size : 25 Test Kits/Box
Cat. No: 195000
The BinaxNOWTM COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset
Product Details:
Number of Reactions(Preps)/Kit : 25
Brand : Roche
ICMR Approved : Yes
Test Method : Antigen Test
Result Time (Rapid Kits) : 10-15 mins
Cat. No : 9901-NCOV-01G
Reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2
The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatopgraphic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx.
This test is an aid in detecting antigen from the SARS-CoV-2 virus in individuals suspected of COVID-19. This product is strictly intended for professional use in laboratory and Point of Care environment
Cat No : COVAG025. GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in nasopharyngeal and oropharyngeal swab from human.
Cat. No : ICO-3000. iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
Corona viruses are enveloped RNA viruses that are distributed broadly among humans, birds and other mammals, that cause respiratory, enteric, hepatic, and neurologic disease.
SPECIFICATIONS:
Whole blood/serum/plasma may be used for testing.
Results available in only 15 minutes.
Easy to use.
Result can be read visually.
No need for an analyser.
Cost effective method for assisting in screening COVID-19 disease.
Cat No : A28523. TaqPath 1-Step Multiplex Master Mix (No ROX) is a fast, single-tube, 4X RT-qPCR mix that provides for sensitive, reproducible detection of up to four different RNA/DNA targets in a single multiplex reaction. Particularly useful for diagnostics, virus detection, and high throughput gene expression workflows, the mix includes thermostable MMLV reverse transcriptase, dNTPs, UNG, and thermostable Fast DNA polymerase all in a single tube. TaqPath is manufactured under a strong ISO13485 quality management system and is designed to produce consistent product performance lot after lot.
This single-tube, 4X format facilitates easy reaction set upâ??just add user-supplied assay and sample (Figure 1). With reproducible performance even in the presence of inhibitors, coupled with stringent quality control to minimize lot-to-lot variation, TaqPath 1-Step Multiplex Master Mix (No ROX) is a superior choice for your multiplex diagnostic testing or development needs.
High sensitivity
To enable reproducible detection of low-titer pathogen and transcripts, TaqPath 1-Step Multiplex Master Mix (No ROX) has been optimized as a higher-concentration 4X master mix that allows you to input more sample into each reaction, increasing sensitivity even in low-volume reactions. Figure 1 shows the consistency of results obtained when detecting 10 copy inputs of RNA target.
Cat. No : 9901-NCOV-01G. Reliable, rapid chromatographic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2
The SARS-CoV-2 Rapid Antigen Test is a reliable, rapid chromatopgraphic immunoassay for the qualitative detection of specific antigens of SARS-CoV-2 present in the human nasopharynx.
This test is an aid in detecting antigen from the SARS-CoV-2 virus in individuals suspected of COVID-19. This product is strictly intended for professional use in laboratory and Point of Care environment.
1186 Rapid Test Kits Suppliers
Short on time? Let Rapid Test Kits sellers contact you.
