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Medical RTD

Leading Distributor / Channel Partner of standard q hiv 1/2 ab test, standard q dengue ns1 ag, standard q dengue ag+ab duo, standard q dengue igm/igg, standard q malaria p.f/ p.v ag and standard q malaria p.f/pan ag from Chennai.
STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test
  • STANDARD Q HIV 1/2 Ab Test

STANDARD Q HIV 1/2 Ab Test

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Product Details:
Number of Reactions(Preps)/Kit30T
BrandSD Biosensor
ICMR ApprovedYes
Result Time (Rapid Kits)10 min
CAT No :RK019-30

STANDARD Q HIV 1/2 Ab 3-Line performs qualitative analysis by detecting antibodies specific to HIV-1 (including Group O) and HIV-2 in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 10 minutes.

  • Easy to use, Easy to read and interpret
  • Discrimination between HIV-1 and HIV-2 antibodies
  • Room temperature storage
  • Performance 
  • Sensitivity : 100% (74/74)/ Specificity : 100% (232/232)
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STANDARD Q Dengue NS1 Ag
  • STANDARD Q Dengue NS1 Ag
  • STANDARD Q Dengue NS1 Ag
  • STANDARD Q Dengue NS1 Ag
  • STANDARD Q Dengue NS1 Ag
  • STANDARD Q Dengue NS1 Ag
  • STANDARD Q Dengue NS1 Ag

STANDARD Q Dengue NS1 Ag

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Product Details:
Number of Reactions(Preps)/Kit20T
BrandSD Biosensor
ICMR ApprovedYes
Result Time (Rapid Kits)15 min
CAT No :RK014-20

STANDARD Q Dengue NS 1 Ag qualitatively analyzes NS1 antigens specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting Dengue NS1 antigens, the initial infection status of Dengue virus can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.

  • Easy to use, Easy to read and interpret
  • Room temperature storage
  • Performance :
  • Sensitivity : 92.9% (184/198) / Specificity : 98.7% (222/225)
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STANDARD Q Dengue Ag+Ab Duo
  • STANDARD Q Dengue Ag+Ab Duo
  • STANDARD Q Dengue Ag+Ab Duo
  • STANDARD Q Dengue Ag+Ab Duo
  • STANDARD Q Dengue Ag+Ab Duo
  • STANDARD Q Dengue Ag+Ab Duo
  • STANDARD Q Dengue Ag+Ab Duo

STANDARD Q Dengue Ag+Ab Duo

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Product Details:
Number of Reactions(Preps)/Kit10T
BrandSD Biosensor
ICMR ApprovedYes
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.

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STANDARD Q Dengue IgM/IgG
  • STANDARD Q Dengue IgM/IgG
  • STANDARD Q Dengue IgM/IgG
  • STANDARD Q Dengue IgM/IgG
  • STANDARD Q Dengue IgM/IgG
  • STANDARD Q Dengue IgM/IgG

STANDARD Q Dengue IgM/IgG

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Product Details:
Number of Reactions(Preps)/Kit20T
BrandSD Biosensor
ICMR ApprovedYes
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)
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STANDARD Q Malaria P.F/ P.V Ag
  • STANDARD Q Malaria P.F/ P.V Ag
  • STANDARD Q Malaria P.F/ P.V Ag
  • STANDARD Q Malaria P.F/ P.V Ag
  • STANDARD Q Malaria P.F/ P.V Ag
  • STANDARD Q Malaria P.F/ P.V Ag
  • STANDARD Q Malaria P.F/ P.V Ag

STANDARD Q Malaria P.F/ P.V Ag

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Product Details:
Number of Reactions(Preps)/Kit40T
BrandSD Biosensor
ICMR ApprovedYes
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 (5µl)
  • Room temperature storage.
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STANDARD Q Malaria P.f/Pan Ag
  • STANDARD Q Malaria P.f/Pan Ag
  • STANDARD Q Malaria P.f/Pan Ag
  • STANDARD Q Malaria P.f/Pan Ag
  • STANDARD Q Malaria P.f/Pan Ag
  • STANDARD Q Malaria P.f/Pan Ag
  • STANDARD Q Malaria P.f/Pan Ag

STANDARD Q Malaria P.f/Pan Ag

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Product Details:
Number of Reactions(Preps)/Kit40T
BrandSD Biosensor
ICMR ApprovedYes
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 (5µl)
  • Room temperature storage
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STANDARD Q Hbsag
  • STANDARD Q Hbsag
  • STANDARD Q Hbsag
  • STANDARD Q Hbsag
  • STANDARD Q Hbsag
  • STANDARD Q Hbsag

STANDARD Q Hbsag

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Product Details:
Number of Reactions(Preps)/Kit30T
BrandSD Biosensor
ICMR ApprovedYes
Result Time (Rapid Kits)10 min
CAT No :RK026-30
Country of OriginMade in India

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)
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Standard Q Filariasis Ag
  • Standard Q Filariasis Ag
  • Standard Q Filariasis Ag
  • Standard Q Filariasis Ag
  • Standard Q Filariasis Ag
  • Standard Q Filariasis Ag
  • Standard Q Filariasis Ag

Standard Q Filariasis Ag

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Product Details:
Number of Reactions(Preps)/Kit25T
BrandSD Biosensor
ICMR ApprovedYes
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
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STANDARD Q Ultra Dot HIV
  • STANDARD Q Ultra Dot HIV
  • STANDARD Q Ultra Dot HIV
  • STANDARD Q Ultra Dot HIV
  • STANDARD Q Ultra Dot HIV
  • STANDARD Q Ultra Dot HIV
  • STANDARD Q Ultra Dot HIV

STANDARD Q Ultra Dot HIV

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Product Details:
Number of Reactions(Preps)/Kit50T
BrandSD Biosensor
ICMR ApprovedYes
Result Time (Rapid Kits)10 min
CAT No :RK022-50
"STANDARD Q Ultra-Dot 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."
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OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test
  • OnSite Typhoid IgG IgM Rapid Test

OnSite Typhoid IgG IgM Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit30T
BrandCTK Biotech
Result Time (Rapid Kits)15 mins
Sample TypeBlood
Test TypeRapid Test
CAT No :R0160C
The OnSite Typhoid IgG/IgM  Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.

Product Description
  • Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
  • Differentiates Between Igg And Igm To Determine Stage Of Infection
  • One Step Procedure Minimizes Operator Error Due To Sample Preparation
  • High Level Of Reproducibility
  • Test Kits Can Be Used And Stored In A Wide Range Of Temperatures

Product Specification:-

  • Brand Name : CTK Biotech
  • Pkg Qty : 1
  • Number Of Items : 30
  • Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action
  • Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)
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OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test
  • OnSite Troponin I Combo Rapid Test

OnSite Troponin I Combo Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit10T
FormCassette
BrandCTK Biotech
Result Time (Rapid Kits)15 min
CAT No :R3002C
The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Troponin I (cTnI) in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL. It can be performed within 15 minutes by minimally skilled personnel, and without the use of laboratory equipment.
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OnSite Chikungunya IgM Combo Rapid Test Kit
  • OnSite Chikungunya IgM Combo Rapid Test Kit
  • OnSite Chikungunya IgM Combo Rapid Test Kit
  • OnSite Chikungunya IgM Combo Rapid Test Kit
  • OnSite Chikungunya IgM Combo Rapid Test Kit
  • OnSite Chikungunya IgM Combo Rapid Test Kit

OnSite Chikungunya IgM Combo Rapid Test Kit

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Product Details:
Number of Reactions(Preps)/Kit30T
BrandCTK Biotech
Result Time (Rapid Kits)20mins
Sample TypeBlood
Test TypeRapid Test
CAT No :R0066C
The OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood.
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OnSite H.Pylori Ab combo Rapid Test
  • OnSite H.Pylori Ab combo Rapid Test
  • OnSite H.Pylori Ab combo Rapid Test
  • OnSite H.Pylori Ab combo Rapid Test
  • OnSite H.Pylori Ab combo Rapid Test
  • OnSite H.Pylori Ab combo Rapid Test
  • OnSite H.Pylori Ab combo Rapid Test

OnSite H.Pylori Ab combo Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit30
BrandCTK Biotech
Result Time (Rapid Kits)20 mins
Sample TypeBlood
Test TypeRapid Test
CAT No :R0191C
The OnSite H. pylori Ab Combo Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies  (IgG, IgM and IgA) against Helicobacter pylori (H. pylori) in human serum, plasma or whole blood.
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OnSite Duo Dengue Ag IgG/IgM Rapid Test
  • OnSite Duo Dengue Ag IgG/IgM Rapid Test
  • OnSite Duo Dengue Ag IgG/IgM Rapid Test
  • OnSite Duo Dengue Ag IgG/IgM Rapid Test
  • OnSite Duo Dengue Ag IgG/IgM Rapid Test
  • OnSite Duo Dengue Ag IgG/IgM Rapid Test

OnSite Duo Dengue Ag IgG/IgM Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit10T
BrandCTK BioTech
Result Time (Rapid Kits)10 min
Sample TypeBlood
Test TypeRapid 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 µL 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)
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TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test
  • TRUST line Filariasis IgG/IgM Combo Rapid Test

TRUST line Filariasis IgG/IgM Combo Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit10T
BrandCTK BioTech
Result Time (Rapid Kits)15 min
Sample TypeBlood
Test TypeRapid 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)


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OnSite FOB-Hi Rapid Test
  • OnSite FOB-Hi Rapid Test
  • OnSite FOB-Hi Rapid Test
  • OnSite FOB-Hi Rapid Test
  • OnSite FOB-Hi Rapid Test
  • OnSite FOB-Hi Rapid Test
  • OnSite FOB-Hi Rapid Test

OnSite FOB-Hi Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit25T
BrandCTK BioTech
Result Time (Rapid Kits)10 min
Sample TypeBlood
Test TypeRapid 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)
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OnSite H.Pylori Ag Rapid Test
  • OnSite H.Pylori Ag Rapid Test
  • OnSite H.Pylori Ag Rapid Test
  • OnSite H.Pylori Ag Rapid Test
  • OnSite H.Pylori Ag Rapid Test
  • OnSite H.Pylori Ag Rapid Test
  • OnSite H.Pylori Ag Rapid Test

OnSite H.Pylori Ag Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit25T
BrandCTK BioTech
Result Time (Rapid Kits)10 min
Sample TypeBlood
Test TypeRapid 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 ≥ 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, α-haemolytics streptococcus, Salmonella Paratyphi B, β-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

  • ndividually 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)
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OnSite HAV IgG/IgM Rapid Test - R0092C
  • OnSite HAV IgG/IgM Rapid Test - R0092C
  • OnSite HAV IgG/IgM Rapid Test - R0092C
  • OnSite HAV IgG/IgM Rapid Test - R0092C
  • OnSite HAV IgG/IgM Rapid Test - R0092C
  • OnSite HAV IgG/IgM Rapid Test - R0092C
  • OnSite HAV IgG/IgM Rapid Test - R0092C

OnSite HAV IgG/IgM Rapid Test - R0092C

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Product Details:
Number of Reactions(Preps)/Kit10
BrandCTK BioTech
Result Time (Rapid Kits)15 min
Sample TypeBlood
Test TypeRapid Test
CAT No :R0092C
  • 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 ≥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 patient’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 µL capillary tubes
  • Sample diluent (REF SB-R0092, 5 mL/bottle)
  • Package insert (instruction for use)
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OnSite HAV IgM Rapid Test
  • OnSite HAV IgM Rapid Test
  • OnSite HAV IgM Rapid Test
  • OnSite HAV IgM Rapid Test
  • OnSite HAV IgM Rapid Test
  • OnSite HAV IgM Rapid Test
  • OnSite HAV IgM Rapid Test

OnSite HAV IgM Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit10
BrandCTK BioTech
Result Time (Rapid Kits)15 min
Sample TypeBlood
Test TypeRapid 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 ≥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 patient’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 µL capillary tubes
  • Sample diluent (REF SB-R0092, 5 mL/bottle)
  • Package insert (instruction for use)
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OnSite HEV IgM Rapid Test
  • OnSite HEV IgM Rapid Test
  • OnSite HEV IgM Rapid Test
  • OnSite HEV IgM Rapid Test
  • OnSite HEV IgM Rapid Test
  • OnSite HEV IgM Rapid Test

OnSite HEV IgM Rapid Test

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Product Brochure

Product Details:
Number of Reactions(Preps)/Kit10T
BrandCTK BioTech
Result Time (Rapid Kits)15 min
Sample TypeBlood
Test TypeRapid Test
CAT No :R0095C
  • 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 ≥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 patient’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 µL capillary tubes
  • Sample diluent (REF SB-R0092, 5 mL/bottle)
  • Package insert (instruction for use).
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OnSite S.Typhi/Paratyphi Ag Rapid Test
  • OnSite S.Typhi/Paratyphi Ag Rapid Test
  • OnSite S.Typhi/Paratyphi Ag Rapid Test
  • OnSite S.Typhi/Paratyphi Ag Rapid Test
  • OnSite S.Typhi/Paratyphi Ag Rapid Test
  • OnSite S.Typhi/Paratyphi Ag Rapid Test

OnSite S.Typhi/Paratyphi Ag Rapid Test

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Product Brochure

Product Details:
Number of Reactions(Preps)/Kit25
BrandCTK BioTech
Result Time (Rapid Kits)15 min
Sample TypeBlood
Test TypeRapid 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).
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OnSite Toxo IgG/IgM Combo Rapid Test
  • OnSite Toxo IgG/IgM Combo Rapid Test
  • OnSite Toxo IgG/IgM Combo Rapid Test
  • OnSite Toxo IgG/IgM Combo Rapid Test
  • OnSite Toxo IgG/IgM Combo Rapid Test
  • OnSite Toxo IgG/IgM Combo Rapid Test

OnSite Toxo IgG/IgM Combo Rapid Test

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Product Brochure

Product Details:
Number of Reactions(Preps)/Kit30T
BrandCTK Biotech
Result Time (Rapid Kits)20mins
Test TypeRapid Test
CAT No :R0234C
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
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STANDARD Q Tsutsugmushi IgM/IgG
  • STANDARD Q Tsutsugmushi IgM/IgG
  • STANDARD Q Tsutsugmushi IgM/IgG
  • STANDARD Q Tsutsugmushi IgM/IgG
  • STANDARD Q Tsutsugmushi IgM/IgG
  • STANDARD Q Tsutsugmushi IgM/IgG
  • STANDARD Q Tsutsugmushi IgM/IgG

STANDARD Q Tsutsugmushi IgM/IgG

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Product Details:
Number of Reactions(Preps)/Kit20T
BrandSD Biosensor
ICMR ApprovedYes
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 (10µl)
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STANDARD Q Chikungunya IgM/IgG
  • STANDARD Q Chikungunya IgM/IgG
  • STANDARD Q Chikungunya IgM/IgG
  • STANDARD Q Chikungunya IgM/IgG
  • STANDARD Q Chikungunya IgM/IgG
  • STANDARD Q Chikungunya IgM/IgG
  • STANDARD Q Chikungunya IgM/IgG

STANDARD Q Chikungunya IgM/IgG

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Product Details:
Number of Reactions(Preps)/Kit20T
BrandSD Biosensor
ICMR ApprovedYes
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 µl)
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STANDARD Q HCV Ab
  • STANDARD Q HCV Ab
  • STANDARD Q HCV Ab
  • STANDARD Q HCV Ab
  • STANDARD Q HCV Ab
  • STANDARD Q HCV Ab
  • STANDARD Q HCV Ab

STANDARD Q HCV Ab

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Product Details:
Number of Reactions(Preps)/Kit30T
BrandSD Biosensor
ICMR ApprovedYes
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)
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STANDARD Q Ultra-Dot HCV
  • STANDARD Q Ultra-Dot HCV
  • STANDARD Q Ultra-Dot HCV
  • STANDARD Q Ultra-Dot HCV
  • STANDARD Q Ultra-Dot HCV
  • STANDARD Q Ultra-Dot HCV
  • STANDARD Q Ultra-Dot HCV

STANDARD Q Ultra-Dot HCV

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Product Details:
Number of Reactions(Preps)/Kit50
BrandSD Biosensor
ICMR ApprovedYes
Result Time (Rapid Kits)10 min
CAT No :RK023-50
STANDARD Q Ultra-Dot 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.
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OnSite Leptospira IgG/IgM Combo Rapid Test
  • OnSite Leptospira IgG/IgM Combo Rapid Test
  • OnSite Leptospira IgG/IgM Combo Rapid Test
  • OnSite Leptospira IgG/IgM Combo Rapid Test
  • OnSite Leptospira IgG/IgM Combo Rapid Test
  • OnSite Leptospira IgG/IgM Combo Rapid Test

OnSite Leptospira IgG/IgM Combo Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit30T
BrandCTK BioTech
Result Time (Rapid Kits)15 min
Sample TypeBlood
Test TypeRapid 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 μmol/L; Bilirubin:  20 mg/dL; EDTA: 3.4 μmol/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
  • 5 μL capillary tubes
  • Sample diluent (REF SB-R0101, 5 mL/bottle)
  • One package insert (instruction for use)
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OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test
  • OnSite Dengue Ag Rapid Test

OnSite Dengue Ag Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit10
BrandCTK BioTech
Result Time (Rapid Kits)20Min
Sample MaterialSerum / Plasma / Whole Blood
Cat. NoR0063c

The OnSite Dengue Ag rapid Test CE is a lateral flow chromatographic immunoassay for the qualitative detection of dengue NS1 antigen (DEN1, 2, 3, 4) in human serum, plasma or whole blood.

The test is designed to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with dengue virus.

Any use or interpretation of this preliminary test result must also rely on other clinical findings and 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 within 9 days consistent with acute dengue infection or dengue fever including: high fever, severe headaches, severe pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash.

Dengue NS1 antigen is detectable in human blood from the first day after the onset of fever up to 9 days, which allows early detection and prompt treatment of infection with dengue virus.

As mild dengue fever symptoms can overlap with acute clinical manifestations of other arbovirus infections, such as Zika virus and chikungunya virus infections, correct diagnosis of dengue infection during early disease onset is critical for guiding clinical patient management.

Product Specification:

  • Individually sealed foil pouches containing:
    • One cassette device
    • One desiccant
  • Plastic droppers
  • Sample diluent (REF SB-R0063, 5 mL/bottle)
  • One package insert (instruction for use)
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OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test
  • OnSite Dengue IgG IgM Combo Rapid Test

OnSite Dengue IgG IgM Combo Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit30
BrandCTK BioTech
Result Time (Rapid Kits)20-25 Min
Sample MaterialSerum / Plasma / Whole Blood
Cat. NoR0061c
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 anti–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 µL Capillary tubes
  • Sample diluent (REF SB-R0061, 5 mL/bottle)
  • One package insert (instruction for use)

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FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test
  • FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test

FIRST RESPONSE Malaria Ag. pLDH HRP2 Combo Card Test

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Product Details:
Number of Reactions(Preps)/Kit25 T
BrandPremier
Result Time (Rapid Kits)20 - 30 Min
CertifiedWHO Aproved
CAT No;PI16FRC25
First Response Malaria Ag. pLDH/HRP2 Combo Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening test for detection of P.falciparum, P. vivax, P. ovale and P. malariae.
  • 100% - Specificity
  • 100% - Sensitivity
  • Rapid Result time within 20 - 30 Minutes.
  • Storage at 1 – 40°C.
  • Detects P.falciparum, P. vivax, P. ovale and P. malariae.
  • Specimen -  Whole Blood
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FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test
  • FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test

FIRST RESPONSE Malaria Antigen P. faciparum(HRP2) Card Test

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Product Details:
Number of Reactions(Preps)/Kit25 T
BrandPremier
Result Time (Rapid Kits)20 -30 MIN
CertifiedWHO Aproved
CAT No;PI13FRC25

First Response Malaria Antigen P.falciparum (HRP2) Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum specific HRP2 antigen.

  • Sensitivity - 100%
  • Specificity - 100%
  • Rapid Result time within 20 - 30 Minutes.
  • Detects Histidine Rich protein(HRP2) of Plasmodium P.falciparum
  • Storage at 1 – 40°C.
  • Specimen Type-  Whole Blood
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FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test
  • FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test

FIRST RESPONSE HIV 1+2 SYPHILIS Combo Card Test

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Product Details:
Number of Reactions(Preps)/Kit25T
BrandPremier
Result Time (Rapid Kits)15 - 20
CertifiedWHO Aproved
CAT No :I20FRC25

First Response HIV 1+2 / Syphilis Combo Card Test is intended for use by healthcare professionals and trained user. It is a rapid, qualitative screening, in vitro diagnostic test for the detection of antibodies (IgG & IgM) specific to HIV (type 1 & 2) and Treponema pallidum in human serum, plasma or venous and capillary whole blood.

  • Sensitivity: 100%
  • Specificity: 100%
  • Storage at 4-30°C
  • Rapid Result time - 15 to 25 Minutes.
  • Detects antibodies specific to HIV and Syphilis.
  • Specimen Type – Whole blood, Serum, Plasma
  • Shelf Life: 24 Months
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First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test
  • First Response SyphiliS Anti-TP Card Test

First Response SyphiliS Anti-TP Card Test

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Product Details:
Number of Reactions(Preps)/Kit25 T
BrandPremier
Result Time (Rapid Kits)20 - 25 Min
CertifiedWHO Approved
CAT No;PI08FRC25
First Response Syphilis Anti-TP Card Test is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative, screening, in vitro diagnostic test for the detection of antibodies of all classes specific to Treponema pallidum in human serum, plasma or Venous or capillary whole blood.
Product specifications :
  • 100% - Specificity
  • 100% - Sensitivity
  • Detects antibodies specific to Treponema pallidum
  • Rapid Result time within 20-25 Minutes
  • Storage at 4-30°C
  • Specimen Type – Whole blood, serum, plasma
  • Shelf Life: 24 Months
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FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test
  • FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test
  • FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test
  • FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test
  • FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test
  • FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test
  • FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test
  • FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test

FIRST RESPONSE HIV 1 - 2.0 CARD TEST (Version 2.0) Rapid HIV card Test

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Product Details:
Number of Reactions(Preps)/Kit30 T
BrandPremier
Result Time (Rapid Kits)15 min
CAT No;PI05FRC30
CertifiedWHO Aproved

First Response® HIV 1-2.O Card Test (Ver. 2.0) is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative screening, in vitro diagnostic test for detection of antibodies specific to HIV-1 (including Group O) and HIV-2 in human serum, plasma or venous and capillary whole blood.

 

Product specifications :

 

  • Sensitivity: 100%
  • Specificity: 100%
  • Detects antibodies specific to HIV-1 (including Group O) and HIV-2.
  • Rapid Result time - 15 to 25 Minutes.
  • Storage at 4-30°C
  • Specimen Type – Whole blood, serum, plasma
  • Shelf Life: 24 Months
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First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test
  • First Response Malaria Ag. P.f.  P.v. Card Test

First Response Malaria Ag. P.f. P.v. Card Test

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Product Brochure

Product Details:
Number of Reactions(Preps)/Kit25 T
BrandPremier
Result Time (Rapid Kits)20 - 30 Min
CAT No;PI19FRC25
CertifiedWHO Approved
First Response® Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
  • Sensitivity - 100%
  • Specificity -100%
  • Rapid Result time within 20 - 30 Minutes.
  • Detects P. falciparum and P. vivax.
  • Storage at 1 – 40°C.
  • Specimen Type-  Whole Blood
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Bioline HIV/Syphilis Duo
  • Bioline HIV/Syphilis Duo
  • Bioline HIV/Syphilis Duo
  • Bioline HIV/Syphilis Duo
  • Bioline HIV/Syphilis Duo
  • Bioline HIV/Syphilis Duo

Bioline HIV/Syphilis Duo

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Product Brochure

Product Details:
BrandAbbott
Result Time (Rapid Kits)15 Mins
SamplesBlood, Serum & Plasma
Box Size25 T
Cat No06FK35CE
BIOLINE HIV/Syphilis Duo test is a solid phase immunochromatographic assay for the qualitative detection of antibodies to all isotypes(IgG, IgM, and IgA) specific to HIV-1/2 and/or Treponema pallidum (TP) simultaneously in human serum, plasma, or whole blood.
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Bioline Malaria Ag P.f / Pan
  • Bioline Malaria Ag P.f / Pan
  • Bioline Malaria Ag P.f / Pan
  • Bioline Malaria Ag P.f / Pan
  • Bioline Malaria Ag P.f / Pan
  • Bioline Malaria Ag P.f / Pan

Bioline Malaria Ag P.f / Pan

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Product Brochure

Product Details:
BrandAbbott
Usage/ApplicationHospital
Results30 min
Test TypeRapid Test
shelf life24 months
Cat. No05FK63I01
Bioline MALARIA Ag P.f/PanTEST FOR P.FALCIPARUM AND OTHER PLASMODIUM SPECIES

The Bioline Malaria Ag P.f/Pan test is a rapid, qualitative and differential test for the detection of histidine-rich protein 2 HRP2 antigen of Plasmodium falciparum and common Plasmodium lactate dehydrogenase (pLDH) of Plasmodium species in human whole blood.

Benefits: 

  • Distinguish P.f infection from other species (P.v, P.m or P.o)
  • Useful in regions where all malaria species are circulating
  • WHO prequalified
  • Specimen : Whole blood (5 μl)
  • Time to result : 15 minutes (up to 30 minutes)
  • 1-40°C for 24 months
  • Performance:
    - P.f (HRP2) : Sensitivity 99.7 %, Specificity 99.5 %
    - Pan (pLDH) : Sensitivity 95.5 %, Specificity 99.5 %
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Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv
  • Bioline Malaria Ag P.f/Pv

Bioline Malaria Ag P.f/Pv

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Product Details:
Number of Reactions(Preps)/Kit25T
BrandAbbott
Time To Result15 Min
Result Time (Rapid Kits)15 min
Sample TypeBlood
Cat. No05FK80
Bioline™ MALARIA Ag P.f/P.vTEST FOR PLASMODIUM FALCIPARUM AND PLASMODIUM VIVAX

The Bioline™ Malaria Ag P.f/P.v test is a rapid, qualitative and differential test for the detection of histidine-rich protein 2 (HRP-2) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood.

BENEFITS

  • Differential diagnosis between Plasmodium falciparum and
    Plasmodium vivax
  • Useful for the region where P.v and P.f are both dominant
  • Differentiate P.f mono infection from P.f/P.v co-infection
  • WHO prequalified
  • Specimen : Whole blood (5 μl)
  • Time to result : 15 minutes (up to 30 minutes)
  • 1-40°C for 24 months
Performance:
  • P.f (HRP2) : Sensitivity 99.7 %, Specificity 99.5%
  • P.v (pLDH) : Sensitivity 95.5 %, Specificity 99.5%



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Bioline HIV 1/2 3.0
  • Bioline HIV 1/2 3.0
  • Bioline HIV 1/2 3.0
  • Bioline HIV 1/2 3.0
  • Bioline HIV 1/2 3.0
  • Bioline HIV 1/2 3.0

Bioline HIV 1/2 3.0

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Product Brochure

Product Details:
Number of Reactions(Preps)/Kit30T
BrandAbbott
ICMR ApprovedYes
Result Time (Rapid Kits)20Min
Self Time24 months
Cat. No03FK10CE
Bioline HIV 1/2 3.0HIV 1/2 ANTIBODY TEST

Bioline HIV 1/2 3.0 test is an immunochromatographic assay for the differential and qualitative detection of all isotypes (IgG, IgM, IgA) antibodies specific to HIV-1 including subtype O and HIV-2 simultaneously, in human serum, plasma or whole blood.

Benefits:

  • Highly sensitive even to IgM during early infection stage
  • Differentiated test result between HIV type I and II by clear band formation (3-lines)
  • Specimen : Serum, Plasma (10 μl), or Whole blood (20 μl)
  • 24 months at 1-30℃
Specification:
  • Sensitivity : 100%
  • Specificity : 99.8%
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Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo
  • Bioline Dengue Duo

Bioline Dengue Duo

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Product Brochure

Product Details:
Number of Reactions(Preps)/Kit10
BrandAbbott
Result Time (Rapid Kits)15 mins
Results15 - 20 min
Cat. No11FK45
Bioline DENGUE DUO (DENGUE NS1 Ag + IgG/IgM)TEST FOR DENGUE INFECTION

The Bioline Dengue Duo kit is a rapid, in-vitro immunochromatographic assay designed to detect both dengue virus NS1 antigen and IgG/IgM antibodies against dengue virus in human serum, plasma or whole blood. Bioline™ Dengue Duo rapid test contains two test devices (left side; Dengue NS1 Ag test, right side; Dengue IgG/IgM test).

Benefits:

  • Simultaneous detection of Dengue Ag & Ab
  • Cover all clinical stages from acute phase to convalescence phase of infection
  • Fast test result : 15~20 min
  • Convenient storage condition : 1~30°C
Specification:
  • Performance
    - Sensitivity : 92.4% (Dengue NS1 Ag), 94.2% (Dengue IgG/IgM)
    - Specificity : 98.4%(Dengue NS1 Ag), 96.4% (Dengue IgG/IgM)

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