Raj Biosis Private Limited

ICMR Approved	Yes
Sample Type	Blood
Brand	S D BioSensor
Usage/Application	Laboratory
Number of Reactions(Preps)/Kit	25 test kit
Packaging Type	Box

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.

ICMR Approved	Yes
Type	Rapid test kits
Brand	J mitra
Number of Reactions(Preps)/Kit	10 test
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

Minimum order quantity: 1 Piece

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.

Number of Reactions(Preps)/Kit	25
ICMR Approved	Yes
Brand	J mitra
Test Method	Antigen Test
Result Time (Rapid Kits)	20 test
Sample Type	Nasal Swab
ICMR(Govt) Approved	Yes
Shelf Life	36 Months

Minimum order quantity: 1 Piece

Intended Use

Covid 19 Ag Card Test is designed for in vitro qualitative detection of Covid 19 antigen in human nasopharyngeal, nasal swab specimens. The kit is intended for professional use and as a screening test and is an aid in early diagnosis of SARS COV-2 infection in patients with clinical symptoms.

Rapid Visual Test for the Qualitative Detection of Covid-19 (SARS-COV-2) antigen in Human nasopharyngeal and nasal swab specimens.

 

• Based on Sandwich Immunoassay principle.
• Results within 20 minutes.
• Single step test procedure.
• Evaluated & Validated by ICMR Centre ; Sensitivity -91.5% (<30 CT) & Specificity -100% against RT-PCR.
• Long Shelf life:30 months at 2-30° C.
• No Instruments required.
• Convenient pack sizes . 10T,25T,50T,100T & 200T.

ICMR Approved	Yes
Brand	wondfo
Number of Reactions(Preps)/Kit	25
Result Time (Rapid Kits)	15min
Sample Type	Blood
Packaging Type	box

Minimum order quantity: 5 Piece

The Finecare fT3 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of free triiodothyronine (fT3) in human whole blood serum or plasma. The test is used as an aid to the assessment of thyroid function

STORAGE AND STABILITY1. Store the test kit at 4℃~30℃ up to the expiration date printed on package.
2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing.
3.Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened

 

 

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Type	Rapid test kits
ICMR Approved	Yes
Brand	J Mitra
Number of Reactions(Preps)/Kit	50 Test kit
Result Time (Rapid Kits)	20 min
Sample Type	Blood

Minimum order quantity: 1 Piece

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

ICMR Approved	Yes
Brand	athenese-Dx
Number of Reactions(Preps)/Kit	30
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

The TRUSTline Scrub typhus IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM antibodies for Orientia tsutsugamushi (Scrub typhus) in Human Serum/ Plasma/ Whole blood specimen.

• 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.

ICMR Approved	Yes
Brand	Athenese-Dx
Number of Reactions(Preps)/Kit	10 test
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

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.

ICMR Approved	Yes
Brand	Athenese-dx
Number of Reactions(Preps)/Kit	10 test
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

The OnSite HAV IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Hepatitis A virus (HAV) in human serum, plasma or whole blood.

• 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, 2-30 °C.

ICMR Approved	Yes
Brand	Athenese-Dx
Number of Reactions(Preps)/Kit	30 test
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

The OnSite Typhoid IgG/IgM2.0 Rapid Test is a lateral flow immunoassay for the qualitative detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum or plasma.

• 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

• Plastic droppers

• Sample Diluent (1 bottle, 5 mL)

• One package insert (instruction for use)

ICMR Approved	Yes
Brand	Athenese-Dx
Number of Reactions(Preps)/Kit	25 test
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

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)

ICMR Approved	Yes
Sample Type	Blood
Brand	Athenese-Dx
Number of Reactions(Preps)/Kit	30 test
Usage/Application	Clinic
Result Time (Rapid Kits)	20 min
Country of Origin	Made in India

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

ICMR Approved	Yes
Brand	Athenese-dx
Number of Reactions(Preps)/Kit	30
Result Time (Rapid Kits)	20min
Sample Type	Blood
Country of Origin	Made in India

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

Number of Reactions(Preps)/Kit	10 Kits
ICMR Approved	Yes
Brand	Athenese-Dx
Result Time (Rapid Kits)	10
Sample Type	Blood
Country of Origin	Made in India

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

ICMR Approved	Yes
Number of Reactions(Preps)/Kit	10 Test
Form	Card
Brand	Athenese-Dx
Result Time (Rapid Kits)	20 min
Sample Type	Blood
One Box	10 test
Country of Origin	Made in India

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

ICMR Approved	Yes
Brand	Athenese-Dx
Number of Reactions(Preps)/Kit	30
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

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)

ICMR Approved	Yes
Brand	Athenese-Dx
Number of Reactions(Preps)/Kit	30 test
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Country of Origin	Made in India

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

Type	Rapid test kits
ICMR Approved	Yes
Brand	J mitra
Number of Reactions(Preps)/Kit	25 test
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Packaging Type	Box

Minimum order quantity: 1 Piece

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%

ICMR Approved	Yes
Sample Type	Blood
Brand	J Mitra
Brand Name	J Mitra
Usage/Application	Clinic
Number of Reactions(Preps)/Kit	25 Test Kit
Result Time (Rapid Kits)	20 Min
Packaging Type	Box

Minimum order quantity: 1 Piece

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.

Sample Type	Blood
ICMR Approved	Yes
Brand	J Mitra
Brand Name	J Mitra
Number of Reactions(Preps)/Kit	25 Test Kit
Usage/Application	Clinic, Hospital, Laboratory
Result Time (Rapid Kits)	20 min
Packaging Type	Box

Minimum order quantity: 1 Kit

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

Sample Type	Blood
ICMR Approved	Yes
Brand	J Mitra
Number of Reactions(Preps)/Kit	50 Test
Usage/Application	Hospital, Laboratory, Clinic
Result Time (Rapid Kits)	20 Min
Packaging Type	Box

Minimum order quantity: 1 Piece

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

Type	Rapid test kits
ICMR Approved	Yes
Brand	J Mitra
Number of Reactions(Preps)/Kit	20 Test
Result Time (Rapid Kits)	20 min
Sample Type	Blood

Minimum order quantity: 1 Piece

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)

ICMR Approved	Yes
Brand	Avantor
Number of Reactions(Preps)/Kit	50 T
Result Time (Rapid Kits)	20 min
Sample Type	Blood
Packaging Type	Box

Minimum order quantity: 1 Piece

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.

ICMR Approved	Yes
Brand	S D Biosensor
Test Method	(SARS-CoV-2) IgM/IgG Rapid Antibody
Result Time (Rapid Kits)	15 min
Sample Type	Blood
Number of Reactions(Preps)/Kit	20test kit

Minimum order quantity: 1 Kit

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.

ICMR Approved	Yes
Brand	S D Biosensor
Test Method	Antigen Test
Result Time (Rapid Kits)	15 min
Sample Type	Blood
Number of Reactions(Preps)/Kit	25 test kit
Sample Type	Blood

Minimum order quantity: 1 Kit

STANDARD F COVID-19 Ag FIA is the fl uorescent immunoassay for the qualitative detection of specific nucleoprotein antigens to SARS-CoV-2 present in human nasopharynx. STANDARD F COVID-19 Ag 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 early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection.

ICMR Approved	Yes
Sample Type	Blood
Brand	S D biosensor
Usage/Application	Laboratory
Number of Reactions(Preps)/Kit	25 kit
Result Time (Rapid Kits)	15 min

Minimum order quantity: 1 Kit

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

ICMR Approved	Yes
Sample Type	Blood
Brand	S D Biosensor
Usage/Application	Laboratory
Number of Reactions(Preps)/Kit	20 Test kit
Result Time (Rapid Kits)	15 minutes

Minimum order quantity: 1 Kit

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.

ICMR Approved	Yes
Sample Type	Blood
Brand	S D biosensor
Usage/Application	Laboratory
Number of Reactions(Preps)/Kit	20 kits
Result Time (Rapid Kits)	15 minutes
Packaging Type	box

Minimum order quantity: 1 Kit

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

ICMR Approved	Yes
Sample Type	Blood
Brand	S D Biosensor
Usage/Application	Laboratory
Number of Reactions(Preps)/Kit	20 test kit
Result Time (Rapid Kits)	15 minutes

Minimum order quantity: 2 Kit

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.

ICMR Approved	Yes
Brand	SD bioline
Shelf Life	18 Months
Usage/Application	Hospital
Packaging Type	Box
Test Result	Up to 20 min
Country of Origin	Made in India

Minimum order quantity: 25 Piece

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

ICMR Approved	Yes
Brand	S D biosensor
Test Method	(SARS-CoV-2) IgM/IgG Rapid Antibody
Result Time (Rapid Kits)	15 min
Sample Type	Blood
ICMR(Govt) Approved	Yes

Minimum order quantity: 1 Piece

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.

ICMR Approved	Yes
Sample Type	Blood
Brand	S D Biosensor
Usage/Application	Laboratory
Number of Reactions(Preps)/Kit	20 test kit

Minimum order quantity: 1 Kit

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

ICMR Approved	Yes
Sample Type	Blood
Brand	S D biosensor
Usage/Application	Laboratory
Number of Reactions(Preps)/Kit	20 test
Packaging Type	box

Minimum order quantity: 1 Kit

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

Test Method	(SARS-CoV-2) IgM/IgG Rapid Antibody
Sample Type	Blood
Packaging Size	50 tests per kit
Sensitivity	Greater than 99%
Shelf Life	24 Months
Result Time	20 minutes
Sample Volume	5ul Whole Blood
Usage/Application	Hospital, Clinic, Path Lab
Packaging Type	Box

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

Brand	Ozone
Sample Type	Blood
Packaging Size	50 Tests
Method	Rapid Test
Usage/Application	Hospital, Clinic, Path Lab
Packaging Type	Box
Results	20 minutes
Country of Origin	Made in India

HIV Rapid Test for detection and differentiation of HIV 1 and HIV 2 antibodies in Human Serum/Plasma/Whole Blood

Temperature	2 to 40 Degree C
Manufactured By	Ozone
Packaging Type	Box
Test Drive	50 Nos
Assay Buffer	2 Vials
Droper	1x50 Nos.
Package Insert	1 No.
Country of Origin	Made in India

Other Details:

• Lateral flow immunoassay for the simultaneous detection and differentiation of anti-Salmonella typhi (S. typhi) IgG and IgM in human serum or plasma.
• Relative Sensitivity: 97% , Relative Specificity: 99.3%, Overall Agreement: 99.1%

Brand	Ozone
Sample Volume	100 ul
Sensitivity	0.5 ng/ml
Specificity	100%
Packaging Type	Box
Packaging Size	10 Test per box
Country of Origin	Made in India

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

Brand	Ozone
Sensitivity	8 Iu/ml
Method	Rapid Test
Packaging Type	Box
Usage/Application	Hospital, Home, Path Lab
Country of Origin	Made in India

So as to accomplish high level of customer trust, we are keenly involved in offering CCP Rapid Test Kit. We offer them at reasonable rates.

Brand	Ozone
Test Results	20 minutes
Sensitivity	0.5 ng/ml
Packaging Type	Box
Usage/Application	Hospital, Clinic, Path Lab
Packaging Size	10 tests
Country of Origin	Made in India

Is It PCT SQ

Rapid Immunochromatographic Assay for the Semi Quantitative Determination of Procalcitonin in Human Serum/Plasma

• Semi quantitative PCT estimation in human specimens
• No reader or instrument required to perform test or for semi quantification
• Allows differentiation between 0.5, 2 and 10 ug/L
• Simple

Number of Reactions(Preps)/Kit	50 Kits
ICMR Approved	Yes
Brand	Avantor
Result Time (Rapid Kits)	50T
Sample Type	Blood
Packaging Type	box

Minimum order quantity: 1 Piece

BeneSphera™ Pro HIV 1/2 3.1 rapid card test is designed for the detection of antibodies against HIV 1 and HIV 2 from human whole blood, serum, and plasma.

• Detects and differentiats HIV 1 and 2
• Qualitative detection of antibody against HIV 1 (Including Group O)
• Better background clearance and line intensity
• Sensitive to detect low antibody titre
• Sensitivity: 100%
• Specificity: 99,92%

BeneSphera™ Pro HIV 1/2 Antibody 3,1 rapid card test is a rapid and visual immunochromatographic assay, intended for the qualitative detection of antibodies against HIV 1 (including group O) and/or HIV 2 from human whole blood, serum, or plasma. It is a screening test and reactive samples should be confirmed using supplemental test (ELISA/ Western blot etc) as per validated HIV test guidelines. For professional in vitro diagnostic use only.

Sample Type	Blood
ICMR Approved	Yes
Brand	Avantor
Brand Name	Avantor
Usage/Application	Hospital, Laboratory, Clinic
Result Time (Rapid Kits)	20 T
Packaging Type	Box

Minimum order quantity: 1 Kit

BeneSphera™ Malaria Pan/Pf Rapid Card Test for the detection of Malaria Ag (pLDH/HRP-II) Pan/P.f.

• Detects and differentiates P. falciparum and other malaria infections
• Low requirement of sample volume (4 μl)
• Detection up to 50 p/μl (WHO requirement is 200 p/μl)
• Better background clearance and line intensity
• Sensitivity: 100%
• Specificity: 99%

BeneSphera™ Malaria Pan/Pf Rapid Card Test is a rapid, self- performing, qualitative, two site sandwich immunoassay utilising whole blood for the detection of P. falciparum specific histidine rich protein-2 (P.f HRP-2) and Pan Malaria specific (PLDH). The test can also be used for specific detection of P. falciparum.