Raj Biosis Private Limited

Bioline Rapid Test kit:-
Syphilis Rapid test kit
Vitamin D rapid test kit
Typhoid IgM/IgG rapid test kit
Maleria PV/PF Rapid test Kit
LH Rapid test kit
HCV Rapid test kit
HBsAg Rapid test kit


#DiagnosticTesting #RapidResults #TestingTechnology #MedicalDevices #HealthcareInnovation #LabTesting #ViralTesting #DiseaseDetection #PublicHealth #InfectiousDiseases #PathogenDetection #HealthScreening #TestingSolutions #PointOfCareDiagnosis #AntigenTest #AntibodyTest #ViralLoadTesting

Bioline product description:-
Dengue IgG/IgM
ALT+AST combo
Chikungunya Ab
Ferritin
FSH
H. pylori-Ab
HCG
HIV Ag/Ab Combo
IGE
Leptospira Ab
Troponin-I



#RapidTestKit #RapidTesting #PointOfCareTesting #COVIDTestKit #RapidDiagnosis #MedicalTesting #InfectiousDiseaseTesting #HealthScreening

Getein rapit test kits  Anti-cpp , Influenza A/B, Testosterone, Dengue Ns1, ASO, D-dimer, SARF-COV-2,Cardic Tropnin, HbA1c, NT-pro BPn

meril rapid test kit-
HCV test kit, Merilscreen covid -19 Antigen detection test, meril Syphils , Maleriya pf/pan Ag, Maleriya pan Ag, Meril Hbs Ag, Meril meriscreen Maleriya PlDH Ag, Degue Ns1 Ag, Tredro HIV 1-2Ab, HIV 1-2Ab

FEATURES

• First line testing kit for detecting dengue infection from day 1 using NS1 Antigen & differential detection of IgM & IgG Antibodies.
• Detects all 4 serotypes of Dengue virus
• 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: 24 months at 2-30°C.

USES:

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.

Malaria P.f/P.v Test is a rapid, qualitative and differential test for the detection of antibodies to Plasmodium falciparum / Plasmodium vivax in human serum, plasma, whole blood.

Description:

• Differential detection of IgG and IgM antibodies
• Dengue IgG/IgM:Serum, Plasma
• Dengue IgG/IgM WB:Serum, Plasma, Whole Blood
• Presumptive differentiation between primary & secondary dengue infections

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%

Advantage Dengue NS1 Ag card is a rapid solid phase Immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen 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.

Salient Features

• Rapid test based on lateral flow technique.
• Detection of Dengue in the seronegative stage i.e. from Day 1 of fever.
• Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4).
• Results with in 20 minutes
• Longer shelf life : 30 months at 2-30°C.
• Convenient pack size : 25 tests
• Sensitivity-96% and Specificity- 98%

Principle

Advantage Dengue NS1 Ag card test is based on immunochromatographic test principle for the detection of Dengue NS1 antigen. 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.

A lateral flow chromatographic immunoassay for the qualitative detection of IgM antibodies to hepatitis E virus (HEV) in human serum or plasma.

• Instant screening test

• Detects IgM anti-HEV in serum or plasma

• Evaluated with BBI HEV serum conversion and HEV mixed titer performance panels

• Useful for identifying acute HEV infections

Each Kit Contains:

• Individually sealed foil pouches containing:

  • One cassette device

  • One desiccant

• 10 µL Capillary tubes

• Sample Diluent (REF SB-R0095,5mL/bottle)

• One package insert (instruction for use)

The OnSite S. Typhi/Paratyphi Ag Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Salmonella typhi (S. typhi) and Salmonella paratyphi (S. paratyphi) antigens in human fecal specimen, serum, plasma, whole blood or blood culture specimen.

• 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

• Test result within 15 minutes allows medical professionals to take immediate action

• High level of reproducibility

• Test kits can be used and stored in a wide range of temperatures

Each Kit Contains:

• Individually sealed foil pouches containing:

  • One cassette device.

  • One desiccant

• Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer

• Plastic droppers

• Patient ID stickers

• Sample Diluent (1 bottle, 5 mL)

• One package insert (instruction for 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.
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: 24 months at 2-30°C.
• Convenient pack sizes: 10 Tests, 30 Tests & 50 Tests.

Principle

I chroma test kit TSH, Hba 1c, T3 , Vitamin D, Troponin T, CRP, D-dimer, CEA, Tn-1 pluse , Covid- 19, PSA
#Hematology:
#BloodDisorders:
#BloodCancer:
#Thrombosis:
#Transfusion
#BoneMarrow:
#Hemoglobinopathies:
#Coagulation:
#FlowCytometry:
#Hematopathology

STANDARD F TnI/CK-MB Combo FIA detects early signs of Acute myocardial infarction with dual testing.
Advantage :-
Diagnosis of Acute myocardial infarction.
Automatic strip recognition by reading the information stored in 2D barcode.
Serum and Whole blood samples available.

STANDARD F T3 is a fluorescent immunoassay for the quantitative measurement of Thyroid Stimulating Hormone level in human serum. This test is to help diagnose thyroid disorder; to monitor the treatment of hypothyroidism and hyperthyroidism.

STANDARD F fT4 is an immunoassay for the quantitative measurement of free thyroxin(fT4) level in human serum. This test is to help diagnose thyroid disorder; to monitor treatment of hypothyroidism and hyperthyroidism.

STANDARD F Influenza A/B FIA (Analyzer+Test device) is a commercially available rapid diagnostics test system. It can perform the test accurately and rapidly within 1.5-10 minutes with the STANDARD F analyzer. STANDARD F Influenza A/B FIA performs qualitative analysis by detecting Influenza virus A type and B type antigens in the nasopharyngeal samples using fluorescence immunochromatography. This product’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. Advantage  Able to perform qualitative analysis with high sensitivity and specificity by using fluorescent substance Objective result - Eliminates the subjectivity of a visual result Automatic strip recognition by reading the information stored in 2D barcode Time saving by early detection - in case of high titer samples, the analyzer automatically show the test results in 1.5 minutes.

STANDARD F TSH-II FIA is a quantitative test for the determination of the thyroid stimulating hormone (TSH) level in human serum and whole blood(EDTA).
Advantage :-Diagnosis of thyroid disorders Monitoring treatment of hypothyroidism and hyperthyroidism

STANDARD F T4 is a quantitative test for the determination of the thyroxin (T4) in human serum. Advantage Diagnosis of thyroid disorders Monitoring treatment of hypothyroidism and hyperthyroid

STANDARD F COVID-19 IgM/IgG Combo FIA is the fl uorescent immunoassay for the qualitative detection of specific antibodies to SARS-CoV-2 present in human serum and whole blood. STANDARD F COVID-19 IgM/IgG Combo FIA should be used with the STANDARD F Analyzers manufactured by SD BIOSENSOR. This test is for in vitro professional diagnostic use and intended as an aid to diagnosis of SARS-CoV-2 infection in convalescent phase of patient with clinical symptoms with SARS-CoV-2 infection.

STANDARD F SARS-CoV-2 Variant nAb FIA is the fluorescent immunoassay for qualitative measurement of circulating neutralizing antibodies against SARS-CoV-2 in human serum and plasma.

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.

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.

Intended Use

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

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 Typhi IgM & IgG Card is a rapid solid phase immuno-chromatographic test for the qualitative differential and simultaneous detection of salmonella typhi (S. typhi) IgM and IgG antibodies in human serum / plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of typhoid infection and in the determination of recent and past infection.

Salient Features

• Rapid qualitative test for differential detection of Salmonella typhi (S.typhi) IgM and IgG Antibodies in Human Serum / Plasma
• Determination of both recent and past infection
• Results within 20 minutes
• Bio-hazard free, fully covered, see-through Device
• Simple & Easy to use Test Procedure
• No Instruments required
• Long Shelf Life: 30 months at 2-30ºC
• Convenient Pack size: 50 Tests

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.

The TRUSTline Malaria Pf/Pv Ag Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Plasmodium falciparum (Pf) and vivax (Pv) antigen in human blood specimen.

• Meets WHO acceptance criteria

• Ease of use, requires minimal training of personnel

• Expanded testing facility options including areas where quality microscopy is not available

• Quick turnaround time to results

• Increased cost effectiveness, no high cost equipment monitoring

• Availability of Positivia external controls

The TRUSTline Syphilis Ab Rapid Test is an effective tool for blood bank screening and early detection of syphilis to facilitate treatment.

A lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM, and IgA) to Treponema pallidum (Tp) in human serum or plasma.

• Detects IgG, IgM, and IgA antibodies facilitating accurate screening during all stages of disease

• Simple test procedure

• Efficient, easy-to-interpret result

• No additional equipment required

• Room temperature storage

The TRUSTline HIV-Ab/Ag 4th Gen Rapid Test detects HIV p24 in addition to IgG and IgM enabling HIV infection to be caught as early as 16 days post-infection.

A lateral flow immunoassay for the qualitative detection of antibodies (IgG, IgM, IgA) to anti-HIV-1 & 2 virus and HIV-1 p24 antigen in human serum, plasma, or whole blood.

• 4th Generation HIV test to detect p24 in addition to IgG and IgM for early detection

• Evaluated by NIB

• Requires only 5 µL of specimen

• Use serum, plasma, or whole blood

• Results available within 15 min to allow prompt action to be taken at the point of care

• Performance validated with BBI low titre panel and Chinese FDA HIV Ab Panel

The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Tropnin I (cTnI) and its complex in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL.

• Point of Care test, suitable for emergency care

• Limit of Detection (LOD) to cTnI complex of 0.3/0.5 ng/ml (S,P & WB)

• LOD is calibrated by NIST standard

• Can be used with serum, plasma, and whole blood.

• Utilizes polyclonal and monoclonal antibody pair to reduce interference

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.

• Uses serum, plasma or whole blood specimen

• No need to avoid certain medications

• Non-invasive, easy to perform procedure

• Time to result is 15 minutes

Each Kit Contains:

• Individually sealed foil pouches containing:

  • One cassette device

  • One desiccant

• Plastic droppers

• Sample Diluent (REF SB-R0191, 5 mL/bottle)

• One package insert (instruction for use)

• Uses serum, plasma or whole blood specimen

• No need to avoid certain medications

• Non-invasive, easy to perform procedure

• Time to result is 15 minutes

Each Kit Contains:

• Individually sealed foil pouches containing:

  • One cassette device

  • One desiccant

• Plastic droppers

• Sample Diluent (REF SB-R0191, 5 mL/bottle)

• One package insert (instruction for use)

• Uses serum, plasma or whole blood specimen

• No need to avoid certain medications

• Non-invasive, easy to perform procedure

• Time to result is 15 minutes

Each Kit Contains:

• Individually sealed foil pouches containing:

  • One cassette device

  • One desiccant

• Plastic droppers

• Sample Diluent (REF SB-R0191, 5 mL/bottle)

• One package insert (instruction for use)

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.

• Uses serum, plasma or whole blood specimen

• Utilizes recombinant antigen derived from the CHIK structure protein

• IgM immunoassay is the most practical lab method

• Distinguish from dengue infection which presents with similar symptoms

Advantage Malaria Card is a visual, rapid and sensitive immunoassay for the qualitative differential detection of P.falciparum (HRP-2) and P.vivax (pLDH) malaria antigen in human blood only.

Salient Features

• Rapid, visual antigen based test for detecting infection with P.falciparum (HRP-2) & P.vivax (pLDH) malaria parasite in whole blood.
• Excellent Sensitivity & Specificity.
• See through Device for easy result interpretation.
• Longer shelf life of 30 months at 4-30° C.
• Easy to interpret colour bands
• Results within 20 minutes.

Advantage P.f. Malaria Card is a rapid, visual and sensitive immunoassay for the qualitative diagnosis of P.falciparum(P.f) specific Histidine-rich protein-(P.f. HRP-2) in human whole blood only.

Salient Features

• Rapid visual antigen based test for detecting infection with P.falciparum (HRP-2) malaria parasite in whole blood.
• Excellent Sensitivity & Specificity as per WHO Malaria RDTs Evaluation.
• Sensitivity of 50 -100 parasites per µl of blood.
• See through Device for easy result interpretation.
• Longer shelf life -30 months, storage at 4-30° C.
• Results within 20 minutes

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

Scrub Typhus (Tsutsugamushi) IgM & IgG Card is a rapid solid phase immuno-chromatographic assay for the qualitative and differential detection of IgM and IgG antibodies to Scrub Typhus antibodies in human serum / plasma. 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

• Rapid ,visual and qualitative Immunoassay.
• Differential detection of IgM & IgG antiobodies to Scrub Typhus (Tsutsugamushi) in Human Serum / Plasma.
• Based on Immunochromatography Technique.
• See through device for easy interpretation of results.
• Results with in 20 minutes
• Shelf life 30 months at 2-30°C
• Convenient pack size: 20T & 50T.
• Sensitivity & Specificity: 100% (In house Evaluation)

BeneSphera™ Hepatitis B rapid card test is designed for the detection Hepatitis B surface antigen from human serum and plasma.

• Detects all major 10 serotypes of HBsAg
• Detection limit: 0,40 IU/ml HBsAg
• Better background clearance and line intensity
• No cross reactivity with Hepatitis A and Hepatitis C 0,5 ng/ml
• Sensitivity: ≥99%
• Specificity: ≥98%

BeneSphera™ Hepatitis-B rapid card test is an in vitro, qualitative, one-step immunochromatographic test for the detection of Hepatitis B surface antigen in human serum or plasma.

Backed by a rich industrial experience, we are engaged in offering a commendable array of Malaria Antigen Rapid Kit.

Is It Troponin I allows for rapid, high quality and sensitive detection of AMI in whole blood in 20 minutes.