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DBU - Medical RDT

Leading Manufacturer 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

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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
Country of OriginMade 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)
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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  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 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 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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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 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

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Product Details:
Number of Reactions(Preps)/Kit10T
BrandCTK Biotech
FormCassette
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

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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

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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

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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

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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
  • OnSite HAV IgG / IgM Rapid Test
  • OnSite HAV IgG / IgM Rapid Test
  • OnSite HAV IgG / IgM Rapid Test
  • OnSite HAV IgG / IgM Rapid Test
  • OnSite HAV IgG / IgM Rapid Test

OnSite HAV IgG / 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 :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

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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 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 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 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 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 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

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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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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 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 - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo
  • STANDARD Q - HIV/Syphilis Combo

STANDARD Q - HIV/Syphilis Combo

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Product Details:
Number of Reactions(Preps)/Kit30 T
BrandSD Biosensor
ICMR ApprovedYes
Result Time (Rapid Kits)10 Min
Cat. NoRK033-30
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 10µl/whole Blood 20 µl.
Sensitivity: HIV 100% & Syphilis 98.8%
Specificity: HIV 99.9%/syphilis 100%/
Time to result: Minimum of 15 minutes.
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Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm
  • Standard Q Lepospira Igg/Igm

Standard Q Lepospira Igg/Igm

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Product Details:
Number of Reactions(Preps)/Kit25 Test
BrandSD Biosensor
Result Time (Rapid Kits)15 Min
Cat. No09LEP10D
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).
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N\'SURE One step Pragnancy Detention Test
  • N\'SURE One step Pragnancy Detention Test
  • N\'SURE One step Pragnancy Detention Test
  • N\'SURE One step Pragnancy Detention Test
  • N\'SURE One step Pragnancy Detention Test

N'SURE One step Pragnancy Detention Test

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Product Details:
BrandRAPHA
CAT No :N116A
Size50 T
Result Time5 Min
UNIQUE FEATURES:
  • EASY TO PERFORM: Rapid, One Step procedure. Test Procedure & interpretation of results printed on individual Pouch
  • HIGHER SENSITIVITY: Sensitivity of 20 mIU/mL of hCG hormone in Urine ensure the early detection of Pregnancy
  • FAST & ACCURATE RESULTS: Results within 5 minutes, Positive results just in 30 seconds
  • BIGGEST TEST WINDOW WIDTH: Test window width of 4mm ensure the clear background and better readability of the test results
  • USER FRIENDLY: Requires no external measurement system. Can be stored at Room Temperature (2 - 30°C).
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OnSite TORCH Panel Rapid Test

OnSite TORCH Panel Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit10 T
BrandCTK BioTech
Test TypeRapid test
Samplehuman serum, plasma, or whole blood
Test time10 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 (≥ 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 Features : 

  • Distinguishes between IgG and IgM in all five TORCH infections
  • Compatible with serum, plasma, and whole blood
  • Results available in 15 minutes
  • Provides semi-quantitative results for Rubella IgG antibodies
  • Distinguishes between HSV-1 and HSV-2
  • Shelf life: 18 months
  • Analytical Sensitivity of IgG Detection: Twenty negative specimens were spiked with appropriate reference standards at various concentrations. Specimens were run on the OnSite TORCH Panel Rapid Test panel member. Defined as the 95% detection level, the limits of detection, or sensitivity, were determined to be as follows:
  1. Toxo: 5 IU/mL LOD; WHO International Standard Anti-Toxoplasma Serum Ig (TOXM)
  2. Rubella: 15 IU/mL (G1); 250 IU/mL (G2); WHO 1st International Standard (RUBI-1-94)
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)
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OnSite RF Rapid Test

OnSite RF Rapid Test

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Product Brochure

Product Details:
Number of Reactions(Preps)/Kit30 T
BrandCTK BioTech
Result Time (Rapid Kits)10 Min
Sample MaterialPlasma/Serum
Test TypeRapid test
Cat. NoR0310C
The OnSite RF Rapid Test is a lateral flow immunoassay for the qualitative detection of all subtypes of rheumatoid factor (RF) in human serum, plasma or whole blood at a sensitivity of 8 IU/ml.

Product Features : 

  • Rapid test to make RF detection simpler and quicker than Latex
  • Detects RF levels as low as 8 IU/mL
  • Detects all RF isotypes including IgM, IgG, and IgA
  • Simple procedure minimizes risk of operator error – no sample preparation required.
  • The results are ready in 10 minutes, which increases diagnostic efficiency.
  • The least complicated RF test- can be performed in any setting by any health care provider with simple training
  • Rapid test format allows room temperature shipping and storage.

Each kit contains:
  • Individually sealed foil pouches containing:
    • One cassette device
    • One desiccant
  • Capillary tubes (5 µL)
  • Sample Diluent ( REF SB-R0310, 5 mL/bottle )
  • One package insert (instruction for use)
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CTK TRUSTline Scrub typhus IgG/IgM Rapid Test

CTK TRUSTline Scrub typhus IgG/IgM Rapid Test

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Product Details:
Number of Reactions(Preps)/Kit30T
BrandCTK BioTech
ICMR ApprovedYes
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


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Dengue Day 1 Test

Dengue Day 1 Test

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Product Details:
BrandJ.Mithra
Test Kit Type:Dengue Test Kit (Rapid)
Sensitivity & SpecificityHigh
Shelf Life:30 months at 2-30 DegreeC
Pack Size:10, 30 & 50 Tests
Cat. NoIR028010
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; ‘C’ (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 “T” 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 :
Sensitivity96% and Specificity– 98%.

Dengue IgM/IgG Antibody test :
Sensitivity95% and Specificity– 97%.




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Advantage MAL Card

Advantage MAL Card

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Product Details:
BrandJ.Mithra
Result Time (Rapid Kits)Within 20 Minutes
Test Kit TypeMalaria Test Kit (Rapid)
Sensitivity & SpecificityExcellent as per WHO Malaria RDTs Evaluation
Cat. NoIR221050
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.




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J.Mitra Hiv Tridot Rapid Test Card

J.Mitra Hiv Tridot Rapid Test Card

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Product Details:
BrandJ.Mithra
Kit TypeHIV Test Kit (Rapid) (Tri Dot)
Sensitivity100% WHO Evaluation
Specificity100% WHO Evaluation
Result TimeWithin 3 Minutes
Cat. NoIR130100
Intended Use:The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG,IgM & IgA) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only.

Salient Features:
  • Rapid visual test ,based on Flow Through Technology.
  • Differential detection of HIV-1 & HIV-2.
  • Detection of group ‘O’ & subtype ‘C’.
  • Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2.
  • 100% sensitivity & 100% specificity as per WHO Evaluation.
  • Shelf life 24 months at 2-8°C
  • Available in convenient pack sizes- 50 Tests and 100 Tests.
  • Results within 3 minutes.
  • No instrument required.
  • In built quality control dot.
Evaluations:

  • WHO Evaluation: Evaluation report from UNAIDS (WHO), CH-1211Geneva,Switzerland Aug 1999 the Sensitivity and Specificity of HIV TRI-DOT is 100 % .The panel used for evaluation of HIV TRI-DOT by Institute of Tropical Medicine, WHO Collaborating Centre in AIDS, Belgium also included HIV-O virus, which was found reactive with HIV TRI-DOT.
  • NIMHANS BANGALORE: Evaluation report from National HIV Reference Laboratories of Government of India , claiming Sensitivity and Specificity of HIV TRI-DOT to be 100 %.
  • CMC VELLORE: Evaluated by Department of Clinical Virology, Christian Medical College & Hospital, Vellore and published in JCM, vol. 38, Issue 2000,claiming 99.5% sensitivity and 99.9% specificity.
  • NARI PUNE: Evaluation Report from National AIDS Research Institute(NARI-Pune) claiming sensitivity & Specificity to be 100 %.
  • Approved by Drug Controller General of India( DCGI) for the usage in Blood Banks.
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HCV TRI-DOT

HCV TRI-DOT

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Product Details:
BrandJ.Mithra
Result Time (Rapid Kits)Within 3 Minutes
Test Kit TypeHCV Test Kit (Rapid)
Sensitivity100% WHO Evaluation
Specificity98.9% WHO Evaluation
Cat. NoHC020100
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 2-8°C


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Hepacard

Hepacard

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Product Details:
BrandJ.Mithra
Test Kit TypeHBsAg Test Kit (Rapid)
DetectsAll the 11 subtype of HBsAg
Sensitivity100% by WHO Evaluation
Specificity100% by PATH USA Evaluation
Cat. NoHB010100
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 2-30°C.
  • 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.


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