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Oscar Troponin-I is an in vitro diagnostic test based on immunochromatographic assay. It is designed for qualitative determination of Cardiac Troponin-I (cTnI) in human serum / plasma as an aid in the diagnosis
of acute myocardial infarction (AMI).

OSCAR HIV-1 and HIV-2 Test is a rapid, qualitative, sandwich immunoassay for simultaneous and differential detection of total antibodies (IgM / IgG / IgA) to HIV-1 and HIV-2 in human serum / plasma / whole blood .

OSCAR Syphilis / TP Test Device is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for qualitative determi- nation of antibodies (IgG/ IgM/ IgA) to Treponema pallidum (TP) a marker for diagnosis of Syphilis.

Pack Size: 50 Test

Syphilis Rapid TestOSCAR Syphilis / TP Test Device is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for qualitative determi- nation of antibodies (IgG/ IgM/ IgA) to Treponema pallidum (TP) a marker for diagnosis of Syphilis.

Pack Size: 50 Tests

The Oscar Kala azar Dipstick Test is a rapid, qualitative, two site sandwich immunoassay for the determination of antibodies to Visceral Leishmaniasis (VL), members of L. donovani, in human whole blood / serum / plasma. Test is based upon detection of anti rK-39 in the specimen.

HCG MidStream Test is a device for the rapid, qualitative and visual detection of hCG in the human urine. This test can be used by self at home or at clinic. Presence of hCG in urine indicates early stage of pregnancy and allows to consult with the doctor / gynecologist for the management of pregnancy and precautions to be taken during the stage of pregnancy.

The Oscar Kala azar Test Device is a rapid, qualitative, two site sandwich immunoassay for the determination of antibodies to Visceral Leishmaniasis (VL), members of L. donovani, in human serum / plasma specimens.

Oscar Typhoid IgM / IgG TEST DEVICE is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane for differential detection of IgM and IgG antibodies to Salmonella typhi (S. typhi) in human serum, plasma or whole blood. For professional use only.

OvaStream is a midstream rapid test based upon sandwich immunoassay for qualitative detection of luteinizing hormone (LH) in human urine as an aid for the detection of ovulation / LH surge.

The Malaria Antigen test - Pf is an in-vitro diagnostic ready to use test based on the principle of lateral flow chromatographic immunoassay for qualitative detection of histidine rich protein (HRP-II) of Plasmodium falciparum (P.f.) in human whole blood.

The Plasmogen is a ready to use lateral flow chromatographic immunoassay for the simultaneous and differentiation detection of antigen of Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) in human whole blood. It is qualitative test is for in vitro diagnostic use only.

Malaria Pan/ Pf Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of Pan LDH antigens of Plasmodium vivax, Plasmodium falciparum, Plasmodium ovale and Plasmodium malariae and Plasmodium falciparum HRP-II, in human whole blood.

H.Pylori TestOscar H.pylori test is a rapid, qualitative, sandwich immunoassay for simultaneous detection of total antibodies (IgM / IgG / IgA) to H. pylori in human serum / plasma. For professional use only.

OSCAR HCV Test is a rapid immunochromatographic assay intended to be used for qualitative detection of antibodies to Hepatitis C virus (HCV) in human serum / plasma.

Malaria Antigen Test (PAN)OSCAR Malaria Pan Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane the detection of Pan LDH antigens of Plasmodium vivax, Plasmodium falciparum, Plasmodium ovale and Plasmodium malariae and Plasmodium falciparumin human whole blood.

Malaria Antigen 
Plasmogen TestThe Plasmogen is a ready to use lateral flow chromatographic immunoassay for the simultaneous and differentiation detection of antigen of Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) in human whole blood. It is qualitative test is for in vitro diagnostic use only.

Malaria Antigen PF TestThe Malaria Antigen test - Pf is an in-vitro diagnostic ready to use test based on the principle of lateral flow chromatographic immunoassay for qualitative detection of histidine rich protein (HRP-II) of Plasmodium falciparum (P.f.) in human whole blood.

OSCAR Corona Antigen test is a one-step rapid, qualitative, sandwich immunoassay. It is used for the detection of N antigen of corona virus in
human nasal swab specimen.

Pack Size: 25 Tests

Diagnos Celiac Card is a visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of anti tTG IgA, IgG & IgM antibodies in Human Serum or Plasma. The assay is intended to be used as an aid in the recognition and diagnosis of Celiac disease.

Salient Features

• Rapid, Visual and Qualitative Antibody Test.
• Excellent Sensitivity: 99.26% & Specificity: 99.50%.
• Results within 20 minutes.
• Long Shelf life 24 months at 2-8°C.
• Bio-hazard free, fully covered, see-through Device.
• No instrument required.

Advantage Malaria PAN+Pf Card is a rapid, visual and sensitive immunoassay for the qualitative diagnosis of infection with P.falciparum and other Plasmodium species (P.falciparum/P.vivax/P.malariae/P.ovale) in human whole blood only.

Salient Features

• Detects P.f. (HRP-2) and PAN(pLDH)
• Individually pouched Single tests- Practical & Safe
• Infection free- See through Device
• Easy to perform test
• Easy to interpret Colour bands
• Results within 20 minutes
• Sensitivity of 100% & Specificity of 99.80%
• Longer shelf life -30 months, storage at 4-30° C

The 4th Generation HIV TRI-DOT + Ag test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 p24 antigen and HIV-1 & HIV-2 antibodies (IgM,IgG & IgA) in Human Serum or Plasma. The test is a screening test for p24 antigen (HIV-1), anti-HIV-1 & anti-HIV-2 and is for in vitro diagnostic use only. It is intended for screening of blood donors or other individuals at risk for HIV-1 & HIV-2 infection and for clinical diagnostic testing.

Salient Features

• Rapid visual test ,based on enzyme immuno assay & Flow Through Technology.
• Rapid test for simultaneous and differential detection of p24 Antigen & antibodies for HIV on the same device.
• Ideal for Blood screening: detects sero-negative HIV Cases.
• Use of gp-41, C terminus of gp120 for HIV-1 antibodies & gp-36 for HIV -2 antibodies.
• Detection of Group ‘0’ & subtype ‘C’ of HIV-1, which is most prevalent in India.
• Unique washing steps for clear Interpretation of Results.
• Evaluated by National Institute of Biologicals- 100 % Sensitivity & 100 % Specificity.
• Long Shelf life: 15 months at 2-8° C.

The 4th Generation DIAGNOS HCV BI-DOT is a visual, rapid, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C Virus in human serum or plasma. The 4th Generation DIAGNOS HCV BI-DOT has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigens.

Salient Features

• Rapid ,visual 4th generation test.
• Based on Flow Through Technology.
• Use of unique combination of Core, NS3, NS4, NS5 antigen.
• Detects all the subtypes of HCV.
• Result with in 3 min.
• Shelf life : 24 months at 2-8°C.
• Sensitivity- 100 %.
• Specificity- 99.8 %

The Diagnos HIV BI-DOT Test is a visual, rapid, sensitive and accurate immunoassay for the detection of HIV-1 & HIV-2 antibodies (IgM,IgG & 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.
• Detection of group ‘O’ & subtype ‘C’ strain of HIV-1 prevalent in Asian subcontinent.
• Use of Envelope antigen; gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2.
• Shelf life 24 Months at 2-8°C.
• Results within 3 minutes.
• No instrument required.
• In built quality control dot.

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

Scrub Typhus IgM/IgG/IgA Card is a rapid solid phase immuno-chromatographic assay for the qualitative detection of IgM, IgG& IgA antibodies to Scrub Typhus in human serum / plasma / whole blood. This test is for in vitro diagnostic use only and is intended as an aid to early diagnosis of Scrub Typhus infection in patient with clinical symptoms.

Salient Features

• Finger prick, rapid, visual and qualitative Immunoassay.
• Detection of all antibodies (IgM, IgG, IgA) to Scrub Typhus (Tsutsugamushi) in Whole blood/serum / plasma.
• Based on Immunochromatography Technique.
• See through device for easy interpretation of results.
• Results within 20 minutes
• Shelf life 30 months at 2-30°C
• Convenient pack size: 25 T.
• Sensitivity & Specificity: 100%

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.

Advantage PAN Malaria Card is a rapid, visual and sensitive immunoassay for the qualitative diagnosis of all four Plasmodium Species (P.falciparum/P.vivax/P.malariae/P.ovale) based on pLDH antigen in human whole blood only.

Salient Features

• Detects infection with Plasmodium species(P.falciparum/P.vivax/P.malariae/P.ovale)
• Excellent Sensitivity & Specificity as per WHO Malaria RDTs Evaluation.
• See through Device for easy result interpretation.
• Longer shelf life -30 months, storage at 4-30° C.
• Results within 20 minutes.

Advantage Leptospira IgM & IgG card is visual, rapid, sensitive and qualitative immunoassay for the detection of Leptospira specific IgM & IgG antibodies in human serum or plasma.

Salient Features

• Rapid qualitative test for differential detection of Leptospira specific IgM and IgG Antibodies in
• Human serum/plasma.
• One step test procedure, add sample & read results
• Infection free see through device.
• Results with in 20 minutes.
• Shelf life of 30 months at 2-30°C.
• Excellent Sensitivity- 99 % and Excellent Specificity- 99.5%

Advantage Chikungunya IgM Card is a visual, rapid, sensitive, qualitative immunoassay for the detection of Chikungunya specific IgM antibodies in human serum or plasma.

Salient Features

• Based on Sandwich Immunoassay principle.
• One step test procedure.
• Results within 15 minutes.
• Bio hazard free, fully covered, see through device.
• No Instruments required.
• Excellent Sensitivity & Specificity.
• Long Shelf life: 30 months at 2-30° C.
• Convenient pack size:10 Tests

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.

Diagnos Dengue card is a rapid solid phase Immuno-chromatographic test for the qualitative 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 for presumptive diagnosis between primary and secondary dengue infection.

Salient Features

• Rapid, visual and qualitative Immunoassay.
• Differential detection of IgM & IgG Antibodies.
• Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4).
• See through device for easy interpretation of results.
• Unique sample processing method ensures highest accuracy in results.
• Results with in 20 minutes.
• Longer shelf life : 30 months at 2-30°C.
• Convenient pack size : 10 tests
• Sensitivity-95% and Specificity- 97%.

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.

Scrub Typhus IgM Quanti Card is a sensitive immuno chromatographic test for the qualitative detection of Scrub Typhus IgM antibodies in human Serum/ Plasma with iQuant Analyzer.This test is for in vitro diagnostic use only and is intended as an aid in the diagnosis of Scrub Typhus infection.

Salient Features

• Principle : Based on most advanced fluorescence immunoassay
• Individually pouched test cartridge, each cartridge is precision engineered with embedded lot data.
• Results within 20 Minutes .
• Results are directly displayed in Scrub Typhus units .
• Sensitivity & Specificity: 100% (In house Evaluation)
• Longer shelf life: 15 Months at 2-8°C.
• Convenient pack size: 25 Tests.
• Prompt service back-up

STANDARD F Norovirus Ag Plus FIA is a rapid, qualitative fluorescent immunoassay to detect norovirus GI and GII genotype in the human fecal specimen. The test is for in vitro diagnostic use and is intended as an aid to early diagnosis of norovirus infection. This is intended for professional use, only for an initial screening test.

STANDARD F Strep A Ag FIA performs qualitative analysis by detecting Group A streptococcal antigens in samples using fluorescence immunochromatography. This product&rsquo;s performance is much higher than that of other products that use the existing Gold conjugate; through STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained.<br />

STANDARD F C. difficile Toxin A/B FIA qualitatively analyzes Clostridium difficile Toxin A/B in human stool specimen using Fluorescent Immunoassay (FIA). With a simple test method, the test result can be obtained within 15 minutes with its high sensitivity and specificity.

<p>STANDARD F Adeno Respi FIA is the fluorescence immunoassay to detect adenovirus infection in human nasal swab and nasopharyngeal swab, identifying existence of adenovirus.</p> <br />

STANDARD F Rota/Adeno Ag FIA is a fluorescent immunoassay for the qualitative detection of the presence of Rotavirus and/or Adenovirus antigens in fecal specimens.

STANDARD F C. difficile GDH FIA qualitatively analyzes Clostridium difficile Glutamate Dehydrogenase (GDH) antigen in human stool specimen using Fluorescent Immunoassay (FIA). With a simple test method, the test result can be obtained within 15 minutes with its high sensitivity and specificity.