Rapid Card
1. Infectious Disease Rapid Test Kits:
* Applications: Used for diagnosing infectious diseases quickly.
* Details: These kits detect specific antigens or antibodies related to diseases like #COVID19, #HIV, #Malaria, and more, aiding in timely treatment.
* Hashtags: #InfectiousDiseaseTesting #RapidDiagnosis #Healthcare
2. Pregnancy Test Kits:
* Applications: Helps individuals determine pregnancy status in the comfort of their homes.
* Details: These kits detect the presence of human chorionic gonadotropin (#hCG) hormone in urine.
* Hashtags: #PregnancyTest #FamilyPlanning #WomensHealth
3. Drug Test Kits:
* Applications: Commonly used for workplace drug testing and substance abuse monitoring.
* Details: These kits detect the presence of drugs, such as marijuana, cocaine, amphetamines, and opioids, in urine or saliva.
* Hashtags: #DrugTesting #WorkplaceSafety #SubstanceAbuse
4. Fertility Test Kits:
* Applications: Helps couples track ovulation and increase their chances of conceiving.
* Details: These kits measure hormone levels, like luteinizing hormone (#LH), in urine to identify fertile days.
* Hashtags: #FertilityTesting #FamilyPlanning #WomensHealth
5. Allergy Test Kits:
* Applications: Identifies allergies to specific substances, aiding in allergy management.
* Details: These kits detect allergen-specific antibodies, such as IgE, in blood or serum.
* Hashtags: #AllergyTesting #AllergyManagement #Health
6. Food Allergen Test Kits:
* Applications: Ensures food safety by detecting allergenic ingredients in food products.
* Details: These kits test for common food allergens like peanuts, tree nuts, gluten, milk, and soy.
* Hashtags: #FoodSafety #AllergenTesting #FoodQuality
7. Environmental Test Kits:
* Applications: Used in environmental monitoring to assess water, air, or soil quality.
* Details: These kits detect pollutants, heavy metals, microbes, or chemical contaminants.
* Hashtags: #EnvironmentalTesting #PollutionControl #Conservation
8. Veterinary Rapid Test Kits:
* Applications: Diagnoses diseases in animals, including livestock and pets.
* Details: These kits help veterinarians identify diseases like brucellosis, foot-and-mouth disease, and parvovirus.
* Hashtags: #AnimalHealth #VeterinaryCare #PetHealth
9. Cardiac Biomarker Test Kits:
* Applications: Used in emergency medicine and cardiology for diagnosing heart conditions.
* Details: These kits detect cardiac biomarkers like troponin and creatine kinase in blood.
* Hashtags: #CardiacHealth #HeartDisease #EmergencyCare
10. Cancer Biomarker Test Kits:
* Applications: Aids in cancer diagnosis and monitoring.
* Details: These kits detect specific tumor markers, such as PSA for prostate cancer or CA-125 for ovarian cancer.
* Hashtags: #CancerDetection #EarlyDiagnosis #Oncology
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
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.
Additional Information:
- Delivery Time: 5-7 days
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
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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
Additional Information:
- Delivery Time: 5-7 days
Backed by a rich industrial experience, we are engaged in offering a commendable array of Malaria Antigen Rapid Kit.
High sensitivity and specificity rapid test kit for HBsAg detection for diagnosis of Hepatitis B Virus in serum/plasma/whole blood.
HIV Rapid Test for detection and differentiation of HIV 1 and HIV 2 antibodies in Human Serum/Plasma/Whole Blood
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%
Is It Troponin I allows for rapid, high quality and sensitive detection of AMI in whole blood in 20 minutes.
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.
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
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.
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody
Additional Information:
- Delivery Time: 10 days
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.
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.
Additional Information:
- Delivery Time: 5-7 days
J mitra rapid test kit:-
Covid 19 Ag Card
Advantage Malaria Card
Advantage Typhi IgM &IgG
Scrub Typhus (IgM+Igg) Card
HIV TRI- DOT
Diagnos Celia card
Hepacard
Advantage MAL card
Dengue Day 1 tast
Advantage Leptospira IgM & IgG card
Advantage chikungunya IgM card
Additional Information:
- Delivery Time: 2-7 days
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
Additional Information:
- Delivery Time: 5-7 days
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)
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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
Additional Information:
- Delivery Time: 5-7 days
Product DescriptionIntended 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.
- Delivery Time: 5-7 days
Additional Information:
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
- Delivery Time: 5-7 days
Additional Information:
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
- Delivery Time: 5-7 days
Additional Information:
Intended Use
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 %.
- Delivery Time: 5-7 days
Additional Information:
Dengue NS1 Antigen FP is a rapid solid phase immuno- chromatographic test for the qualitative detection of Dengue NS1 Antigen in human Whole Blood/ 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 ,visual test for the qualitative detection of Dengue NS1 Antigen in whole blood/serum/Plasma.
- Sample can be taken from Finger prick and sample required is 4µl.
- Based on Sandwich principle.
- Detection of Dengue in Seronegative stage i.e From Day 1 of fever.
- Detection of all 4 serotypes of dengue virus.
- Reliable diagnosis of both primary and secondary infection.
- 100% Sensitivity & 99.96 % Specificity.
- Shelf life: 24 month at 2-30 °C
- Convenient pack Size: 10 Test.
- Evaluated By Referral Medical college / Hospitals /Research institutes / Labs.
- Delivery Time: 5-7 days
Additional Information:
Dengue NS1 Antigen FP is a rapid solid phase immuno- chromatographic test for the qualitative detection of Dengue NS1 Antigen in human Whole Blood/ 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:
- 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.
- Delivery Time: 5-7 days
Additional Information:
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.
- Delivery Time: 5-7 days
Additional Information:
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.
- Delivery Time: 5-7 days
Additional Information:
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
- Delivery Time: 5-7 days
Additional Information:
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
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
Dengue NS1 Antigen self-test is a rapid solid phase immune-chromatographic test for the qualitative detection of Dengue NS1 Ag in human whole blood/serum/plasma. This test is intended to be for home use with self-collected whole blood specimens from individuals aged 18 years or above( or collected by adults for individuals below 18 years of age) as well as for professional use with venous Whole blood/Serum/Plasma samples. This test is for in-vitro diagnostic use only & is designed as an aid in the early diagnosis of dengue infection patients with clinical symptoms.
Salient Features:
- Rapid, Visual, Home test for qualitative detection of Dengue NS1 antigen detection in human whole blood/serum/plasma.
- Finger prick sample can be used.
- Single test pack.
- All material to perform the test & its disposal are provided with the kit.
- Based on Sandwich principle.\
- Detection of Dengue in Seronegative stage i.e. from Day 1 of fever.
- Detection of all 4 serotypes of dengue virus.
- Reliable diagnosis of both primary and secondary infection.
- 100% Sensitivity & 100 % Specificity.
- Shelf life: 30 month at 2-30 °C.
Additional Information:
- Delivery Time: 5-7 days
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%
Additional Information:
- Delivery Time: 5-7 days
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%
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
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.
Additional Information:
- Delivery Time: 5-7 days
Hence detection of both IgM & IgG is significant for the diagnosis of Dengue. Result Interpretation. Reactive for IgM &. IgG Antibodies. Reactive for IgG.
Additional Information:
- Delivery Time: 5-7 days
Trust Line Rapid test kit:-
Chikunguniya IgM Combo Rapid Test kit
Covid -19 Ab Rapid Test kit
Covid -19 Ag Rapid Test Kit
Dengue Ag Rapid Test kit
Duo Dengue Ag+IgG/ IgM Rapid Test kit
Filariasis IgG/IgM Rapid Test Kit
FOB-HI Rapid Test
H. pylori Ab Combo Rapid Test Kit
H.Pylori Ag Rapid Test kit
HAV IgG/IgM Rapid Test Kit
HAV IgM Rapid Test Kit
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
he 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 TRUSTline Duo Dengue Ag-IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG anti-dengue virus, IgM anti-dengue virus and dengue NS1 antigen (DEN1, 2, 3, 4) in human serum, plasma or whole blood.
-
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
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 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
Syphilis Ab Rapid Test (Strip) 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 including 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 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 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 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)
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)
The OnSite Leptospira IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay that can be performed within 15-20 minutes by minimally skilled personnel, and without the use of laboratory equipment.
-
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: 2 g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L
-
Shelf life: 24 month
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 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.
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.
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 H. pylori Ag Rapid Test is a lateral flow chromatographic immunoassay for qualitative detection of H. pylori antigen in human fecal specimen. It is a noninvasive diagnostic method and can be performed within 10 minutes by minimally skilled personnel, and without the use of laboratory equipment.
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 H. pylori.
The OnSite H. pylori Ag Rapid Test detects antigen present in the feces by using specific antibodies, which indicates an active H. pylori infection. However, a negative test result does not preclude the possibility of infection with H. pylori. It can also be used to monitor the effectiveness of treatment and the recurrence of an infection, and is not affected by the use of Proton Pump Inhibitors (PPI). It is reported that the seroprevalence of H. pylori in specimens with positive fecal occult blood (FOB) test results is approximately 39.3%. Therefore a specimen that tests positive with an FOB test may also be tested positive with the OnSite H. pylori Ag Rapid Test. 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.
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
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
Oscar Rapid Test Kit:-
Chikungunya Test kit
Dengue Antigen( Ns1)
Dengue Antibody
H Pylori
Hepatities B Antigen Test
HCV test kit
HIV 4th Genration
HIV-1 &HIV-2 test
Typhoid Test
LH/ Ovulation test
#RapidTestKit
#RapidTesting
#RapidDiagnosis
#PointOfCareTesting
#QuickResults
#DiagnosticTesting
#HealthScreening
#InfectiousDiseaseTesting
#TestingTechnology
#PublicHealthTools
#MedicalDevices
#HealthcareInnovation
#TestAndTrace
#HealthMonitoring
#COVID19Testing
Oscar HCG card test is intended used for qualitative detection of (HCG) in human urine as in aid of early pregnancy detection.
Oscar rapid card-
Dengue Antibody+Antigen (combo)
maleria -pan
Maleriya pF
Maleriya Plasmogen
Maleriya (Pan/PF)
Maleriya PPOCT
Maleriya PV/PF
kala azar test kit
Syphilis Rapid Test
Syphilis Antibody Strip Test
Rapid test
Rapid diagnostic test
Point-of-care testing
Rapid antigen test
Rapid antibody test
Rapid molecular test
Rapid screening
Rapid detection
Rapid testing technology
Rapid test kit
Rapid result test
POC test
Lateral flow test
Immunoassay
Qualitative rapid test
Quantitative rapid test
Rapid test accuracy
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
Fostered with enormous business understanding of this realm, we are involved in presenting a broad consignment of Medsource Dengue Rapid Test Kit.
HBsAg
HCG strip
HIV 1/2
Scrub Thphus
Syphilis AB
Syphilis test
Leptospirosis IgG/ IgM
Dengue Combo(Ns1+IgG/IgM)
Rapid test for detection of hcv antibodies in human serum, plasma or whole blood using recombinant hcv antigens. Covid 19 Antigen.
Maleriya Antigen pf/pv
Maleriya PF/PAN
Tyhoid IgG/IgM
Covid 19 IgM/IgG
HAV IgM
HEV IgM
HIV Ag/Ab
Troponin I
Pregnancy Card Single test
PCT SQ
CCP
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
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
Getein rapit test kits Anti-cpp , Influenza A/B, Testosterone, Dengue Ns1, ASO, D-dimer, SARF-COV-2,Cardic Tropnin, HbA1c, NT-pro BPn
Additional Information:
Item Code: 1100
Delivery Time: 10
Packaging Details: The One Step Test for D-Dimer (colloidal gold) is intended for use together with the The product employs colloidal gold immunechromatogrphy to determine D-Dimer in human plasma, or whole blood specimens. Two monoclonal antibodies are employed to identify D-Dimer specifically, resulting in a purplish red streak appears on the test line. The color intensity of the test line increases in proportion to the concentrations of D-Dimer. Then insert test card into the FIA8000 Quantitative Immunoassay Analyzer, the concentration of D-Dimer is measured quantitatively and displayed on the screen. The result can be transmitted to the lab or hospital information system. Products Code: CG 1006 Detection Method: colloidal gold, a quantitative test for use with the FIA8000 Quantitative Immunoassay Analyzer. Detection Range: 0.1-10.0 mg/L Cut-off Value: 0.5 mg/L Sample Type: plasma or whole blood in Sodium Citrate. Reaction Time: yields results in about 7 minutes. Storage Temperature: 4-30¿¿C Storage Life: 24 months. Use the test card within 1 hour once the foil bag is opened. Package A box package contains 25 tests: Foil bag, which contains one test card and one desiccant 25 Disposable pipet 25 Manual 1 SD card 1 Sample diluent 25
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.
Additional Information:
- Delivery Time: 10 Days
Trust Line Rapid Test Kit:-
HBsAg Rapid Test Kit
HCV rapid Test Kit
HEV IgM Rapid Test kit
HIV Ab/Ag rapid Test Kit
HIV Ab/Ag Rapid Test Kit
Leptospira IgG/IgM Combo Rapid Test kit
Maleria Pf/Pan Rapid Test Kit
S.Typhi Ag rapid Test Kit
Scrub Typhs IgG/IgM Rapid test kit
Syphilis Ab Rapid Test kit
Troponin I Rapid Test kit
Typhoid IgG/IgM Rapid Test Kit
BeneSphera™ Syphilis rapid card test for the detection of antibodies to Syphilis from human serum, plasma, and whole blood.
- No assay buffer required
- User friendly
- Can detect antibody from serum/plasma
- Sensitivity: 100%
- Specificity: 99,8%
- Test time: 10 to 15 min
BeneSphera™ Syphilis rapid card test is a solid phase immunochromatographic assay for the rapid, qualitative, and differential detection of antibodies to Treponema pallidum in human serum or plasma. This test is intended for professional use and provides only a preliminary test result.
Additional Information:
- Delivery Time: 5-7 Days
Features:-
Rapid test device for qualitative detection of hepatitis B surface antigen in human serum or plasma.
BloodDiseases#BloodTests#BloodCount#MDS (Myelodysplastic Syndromes)#Hematopoiesis#MPN (Myeloproliferative Neoplasms)#BMT (Bone Marrow Transplant)#Thalassemia#Hemato#Hemostasis#BloodClots#Hemoglobin#FlowCytometry#HematologyLab#TransfusionMedicine#HematologyNursing#Hemoglobinopathies#HematologyCases#BloodDonation#IronDeficiency#BloodSmear#HematologyTechnician#HemoglobinElectrophoresis#HemolyticAnemia#MyeloproliferativeDisorders#HemophiliaAwareness#BloodCancerAwareness#HematologyNews#HematologyGuidelineslogyEducation
Additional Information:
- Delivery Time: 2-7 Days
- Packaging Details: OZOTEX Widal (4x5)ml
Description:
Malaria Pf/Pv is a rapid, qualitative immunoassay for the detection of P. falciparum specific histidine rich protein -2 (Pf HRP-2) and Pv malaria specific Parasite lactate dehydrogenase (pLDH) in human blood as an aid in the diagnosis of Malaria infection This test also used to differentiate the P. falciparum and the other malarial species. This test is very sensitive and rapid. Results are interpreted in less than 20 minutes. Test results are read visually without any instruments.
BloodDiseases#BloodTests#BloodCount#MDS (Myelodysplastic Syndromes)#Hematopoiesis#MPN (Myeloproliferative Neoplasms)#BMT (Bone Marrow Transplant)#Thalassemia#Hemato#Hemostasis#BloodClots#Hemoglobin#FlowCytometry#HematologyLab#TransfusionMedicine#HematologyNursing#Hemoglobinopathies#HematologyCases#BloodDonation#IronDeficiency#BloodSmear#HematologyTechnician#HemoglobinElectrophoresis#HemolyticAnemia#MyeloproliferativeDisorders#HemophiliaAwareness#BloodCancerAwareness#HematologyNews#HematologyGuidelineslogyEducation
Additional Information:
- Delivery Time: 2-7 Days
- Checks pregnancy status by testing your urine.
- Very simple and easy to use one-step pregnancy tester kit.
- Detects the presence of HCG hormone in the strip.
- Contains a testing device and a disposable dropper.
BloodDiseases#BloodTests#BloodCount#MDS (Myelodysplastic Syndromes)#Hematopoiesis#MPN (Myeloproliferative Neoplasms)#BMT (Bone Marrow Transplant)#Thalassemia#Hemato#Hemostasis#BloodClots#Hemoglobin#FlowCytometry#HematologyLab#TransfusionMedicine#HematologyNursing#Hemoglobinopathies#HematologyCases#BloodDonation#IronDeficiency#BloodSmear#HematologyTechnician#HemoglobinElectrophoresis#HemolyticAnemia#MyeloproliferativeDisorders#HemophiliaAwareness#BloodCancerAwareness#HematologyNews#HematologyGuidelineslogyEducation
Additional Information:
- Production Capacity:Test Device 1N, Dessicant pouch 1N, Instruction manual 1N
Product Description:
HIV 1/2/0 Tri-Line Human Immunodeficiency Virus Test Device - Whole Blood/Serum/Plasma Sailent Features
Based on Principle of Chromatographic Immunoassay
Multiple Detection HIV 1, HIV 2 and HIV O
High Sensitivity & Specificity
Reliable & Economical
Result in minutes
Pack Size: 1x30 Test
Recombigen Rapid Test Kit:-
Typhi IgG/IgM
Troponin-I Card
FSH Card
LH card -Clear ovu
Clear & Sure Pregnan
Preg Card- Clear R
Clearsing Pregnancy Test
Midstream Pregnancy Test
Dengue IgG/IgM Card
Dengue Ns1/IgG/IgM combo
Dengue Ns1
Malaria PF/Pan
Malaria PF/PV
Clear Syphi Syphilis
Syphilis Strip 100T
S D Biosensor Rapid and Elisa Test kit:-
HBsAg
HCV Ab
HiIV 1-2 Ab
Maleriya PF Ag
Maleriya PF/PV Ag
Maleriya PF/PAN Ag
Maleriya Pan Ag
RAS FIA
S. pneumoniae Ag
Strap A ag FIA
Tsutsugamushi IgM-IgG
S D Biosensor rapid kit and Elisa kit:-
Covid IgM/IgG combo
Covid Igm/IgG
Chikungunya IgM/IgG
Dengue Ns1 Ag
Dengue Ag/Ab Duo
Dengue IgG Capture Elisa
Dengue IgM
DEngue Ns1 Ag Elisa
Legionella Ag FIA
Influenza A/B Fia
Dengue Ns1 / Ag
nCov (Real Time Detection Kit)
Roche Cardiac Control Troponin-T
5 cards each Box
Product Description
Qualitative detection of troponin in anticoagulated (EDTA or heparin) venous whole blood.
Test can be used immediately after removal from the refrigerator.
Roche Cardiac Control Troponin-T
Product Description
Roche's CARDIAC POC Troponin T Test is a rapid diagnostic tool for suspected acute myocardial infarction and the detection of patients at increased risk of mortality. The test strip provides reliable cardiac TnT (Troponin T) values over a wide quantitative measurement range (40 - 2000 ng/l).
#Hematology:
#BloodDisorders:#BloodCancer:
#Thrombosis:
#Transfusion
#BoneMarrow:
#Hemoglobinopathies:
#Coagulation:
#FlowCytometry:
#Hematopathology
Oscar Syphilis Card test is intended used for qualitative detection of antibodies (IgM/IgG/IgA) of Treponema pallidum (TP) in human serum / plasma as in aid of Syphilis diagnosis. It is for in-vitro diagnostic use only. The test is based upon immuno-chromatographic principle. Recombinant proteins of TP have been used in the test formulation to make it highly sensitive and specific. Serum / plasma can be used for testing. No buffer & no dilution of sample are required for performing the test. Oscar Syphilis Card test has shelf life of 24 months from date of manufacturing if stored at 2-30°C under sealed condition. Each kit of Oscar Syphilis Card test contains 50 pcs of individually sealed pouches containing test cards and disposable sample dropper. Test can be performed using two-three drops of serum / plasma and result can be read within 5-10 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).
Additional Information:
- Delivery Time:5-7 days
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.
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.
Additional Information:
- Delivery Time:5-7 days
- Delivery Time:7-10 days
- 29012 hexagon ige 20 tests allergy
- 27032p hexagon troponin 20 tests cardiac marker
- 25052 humadrug cannabinoids (thc) 30 tests drugs of abuse
- 25022 humadrug cocaines (coc) 30 tests drugs of abuse
- 25042 humadrug methamphetamines (met) 30 tests drugs of abuse
- 25032 humadrug opiates (opi) 30 tests drugs of abuse
- 58002 hexagon chagas 20 tests infectious diseases
- 58012 hexagon chlamydia 30 tests infectious diseases
- 58912 hexagon chlamydia collect 60 tests infectious diseases
- 58082 hexagon dengue 25 tests infectious diseases
- 58022 hexagon h. Pylori 20 tests infectious diseases
- 58003 hexagon hbsag 1-step 3 x 20 tests infectious diseases
- 58072 hexagon hcv 40 tests infectious diseases
- 57004p hexagon hiv 100 tests infectious diseases
- 57002p hexagon hiv 40 tests infectious diseases
- 58054 hexagon malaria combi device 25 tests infectious diseases
- 58092 hexagon rota 20 tests infectious diseases
- 58062 hexagon strep a 20 tests infectious diseases
- 58042 hexagon syphilis 20 tests infectious diseases
- 58032 hexagon tb 20 tests infectious diseases
- 50291 humatex febrile antigens/brucella abortus 8 x 100 tests infectious diseases
- 50200 humatex febrile antigens/control pc/nc 2 x 2 ml infectious diseases
- 50201 humatex febrile antigens/multiscreening kit 6 x 100 tests infectious diseases
- 50211 humatex febrile antigens/s. Paratyphi ah 8 x 100 tests infectious diseases
- 50221 humatex febrile antigens/s. Paratyphi ao 8 x 100 tests infectious diseases
- 50241 humatex febrile antigens/s. Paratyphi b0 8 x 100 tests infectious diseases
- 50231 humatex febrile antigens/s. Paratyphi bh 8 x 100 tests infectious diseases
- 50251 humatex febrile antigens/s. Paratyphi ch 8 x 100 tests infectious diseases
- 50261 humatex febrile antigens/s. Paratyphi co 8 x 100 tests infectious diseases
- 50271 humatex febrile antigens/s. Typhi h 8 x 100 tests infectious diseases
- 50281 humatex febrile antigens/s. Typhi o 8 x 100 tests infectious diseases
- 50301 humatex salmonella kit 8x100 tests infectious diseases
- 50023 humatex toxo 100 tests infectious diseases
- 40039 im quick test 20 tests infectious diseases
- 40038 im quick test 40 tests infectious diseases
- 50001 syphilis rpr test 100 tests infectious diseases
- 50002 syphilis rpr test 500 tests infectious diseases
- 50016 syphilis rpr test economic kit, reduced accessories 500 tests infectious diseases
- 50101 syphilis tpha test 100 tests infectious diseases
- 60022 fertitex mono 100 tests pregnancy
- 68902 hexagon hcg 1-step 3 x 20 tests pregnancy
- 68932 hexagon hcg 1-step 3 x 50 tests pregnancy
- 68004 humapreg 40 tests pregnancy
- 40037 glycin-nacl buffer 100 ml rheumatology
- 40063 humatex aso 100 tests rheumatology
- 40062 humatex aso 40 tests rheumatology
- 40060 humatex aso latex reagent 100 tests rheumatology
- 40043 humatex crp 100 tests rheumatology
- 40042 humatex crp 40 tests rheumatology
- 40040 humatex crp latex reagent 100 tests rheumatology
- 40053 humatex rf 100 tests rheumatology
- 40052 humatex rf 40 tests rheumatology
- 40050 humatex rf latex reagent 100 tests rheumatology
- 40031 sle latex test 20 tests rheumatology
- 40030 sle latex test 50 tests rheumatology
- 28220 hexagon obscreen 30 x 3 tests tumor marker
- 28009 hexagon obti 24 tests tumor marker
- Rapid ,visual test for the qualitative detection of Dengue NS1 Antigen in whole blood/serum/Plasma.
- Sample can be taken from Finger prick and sample required is 4µl.
- Based on Sandwich principle.
- Detection of Dengue in Seronegative stage i.e From Day 1 of fever.
- Detection of all 4 serotypes of dengue virus.
- Reliable diagnosis of both primary and secondary infection.
- Dengue NS1 Antigen FP is an immunoassay based on the "sandwich" principle. Dengue NS1 antigen device contains two lines; "C" (Control Line) & "T" (Dengue NS1 Antigen detection Test Line). Test line is coated with anti-dengue NS1 antibodies. When a sample is added to the device, Dengue NS1 antigen if present in the sample will bind to the anti-dengue NS1 gold colloid conjugate making antigen antibodies complex. On addition of assay buffer, this complex migrates along the membrane to the test region and forms the visible pink line at "T" as antibody-antigen-antibody gold conjugate complex.
- The intensity of the test band in the device will vary depending upon the amount of antigen present in the sample. The appearance of any pink/red colour in test region should be considered as reactive for Dengue NS1 antigen. A red procedural control line should always develop in the test device window to indicate that the test has been performed properly.
- Multiple Channels High throughput with 80 T/H, 7 test channels + 1 emergency test channel Multiple test items can be tested at the same time, saving operation time Consists of Lyophilized Bead which increases precision, stability, and sensitivity Pre-dilution: › Enough time for antibody-antigen reaction › To obtain better linearity for higher value samples.
- Android system, touch screen Immediate edit of patients' information RFID card calibration and touch for recognition Convenient for viewing test results
- Up To 144 Sample Tubes
- Continuous Loading, Stat Available
- Analyzer Auto Numbered
- Lis Connection
- Refrigerated Sample Area With Independent Power Supply
- Integrated Kit, Ready-To-Use, No Pretreatment Required
- Integrated Kit Including Calibrators
- Using Superparamagnetic Microbeads
- Rfid Tag Storing All Info Of Reagent
- Rfid Tag With Built-In Master Curve
- 2-Point Calibration To Adjust Master Curve
- Optimized for field diagnostics with small size (Clinic, Laboratory)
- Recognize information stored in 2D barcode
- Internal quality control
- LIS/HIS connectivity
-
Fully Portable Battery and/or AC power), Lightweight Reader
-
High Throughput Patient Testing: 30 tests/hr
-
Widest Test Menu on a Single Platform: 44 Parameters across 8 Therapeutic Test Profiles
-
Large Memory: 1000 Samples, 1000 QC & 100 IDs
-
Convenient: 7” Colour Touch Screen, User-Friendly Interface
-
Smart Calibration Chip: No Reagent Wastage & Calibration Failure
-
Internal & External Quality Controls available
-
LIS/HIS Compatible
-
Enhanced Data Management & Connectivity: USB port/Ethernet/SD card slot
Angstrom Biotech Angcard all rapid card-
Angcard Malaria, Angcard Thphoid, Angcard Dengue Ns1 Antigen,
Angcard Dengue combipack, Angcard Urostrom, HDL-C- Direct kit, Angcard Hepatitis - b card, Hepatitis -C card, Angcard Chikungunya, Albumin -Slr kit, sypjhilis strip
Additional Information:
Rapid Screening Human Diagnostic Germany Strips rapid screening part no product size product group:
Rapid detection of antibodies towards Salmonella Typhi/paratyphi in Human Serum/Plasma for diagnostics purpose.
The SD Bioline Malaria Ag P.f/Pv test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood.
Intended Use:
Dengue NS1 Antigen FP is a rapid solid phase immuno- chromatographic test for the qualitative detection of Dengue NS1 Antigen in human Whole Blood/ 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:
Principle:
Fine Care Fluorescence Analyzer is a portable instrument for fluorescence detection to quantify concentration of various kind of analytes in blood. It can be used both in a central laboratory and a point-of-care testing facility. Finecare Analyzer uses a laser as the excitation light source.The emitted light from the fluorescence dye is collected and converted into an electrical signal. The signal is closely related to the amount of fluorescing dye molecules present on the spot under examination. Finecare FIA Meter is full quantitative detection, with small size, simple operation and multiple test items in one machine
Finecare™ FIA Meter Plus is a fluorescence immunochromatographic analysing system with internal temperature control, which can help diagnose conditions such as infection, diabetes, cardiovascular diseases, renal injury and cancers, etc.
Getein1100 Immunofluorescence Quantitative Analyzer is an advanced on-site diagnostic analyzer, intended to deliver accurate testing results in minutes just from 3-4 drops of human specimens.
Test Items Cardiac Marker —— cTnI, NT-proBNP, D-Dimer, CK-MB, NT-proBNP/cTnI, CK-MB/cTnI/Myo, H-FABP Renal Function —— CysC, mAlb, NGAL, β2-MG Inflammation Monitoring —— hs-CRP+CRP, PCT Diabetes —— HbA1c Fertility
Product DescriptionWe are successfully meeting the varied requirements of our clients by providing the best quality range of Maglumi 800 Fully Automatic Immunoassay Analyzer.
Product DescriptionWe are successfully meeting the varied requirements of our clients by providing the best quality range of Maglumi 800 Fully Automatic Immunoassay Analyzer.
We are successfully meeting the varied requirements of our clients by providing the best quality range of Maglumi 800 Fully Automatic Immunoassay Analyzer.
The analyzer is intended for use by healthcare professionals to improve the way to diagnosing and monitoring various conditions, including COVID-19, diabetes, renal injury, cardiovascular disease, pregnancy, inflammation, tumor, etc.
Cipla Cip Point Immunofluorescence Quantitative Analyzer:-
Product DescriptionWith an objective to fulfill the ever-evolving demands of our clients, we are engaged in offering a wide assortment of Maglumi 1000 Fully Automated Immunoassay Analyzer.
STANDARD F200 Analyzer is a fluorescence immunoassay device that can perform qualitative and quantitative analyses on infections, respiratory diseases and chronic diseases, and it supports convenient user interface and LIS/HIS connectivity. Advantage
Product DescriptionMAGLUMI X3 is a CLIA analyzer with a compact but comprehensive design that ensures excellent performance, such as the latest intelligent washing technology and bidirectional temperature control measurement. It has a maximum throughput of 200 tests per hour, 20 reagent positions, 72 sample positions and a single reaction cup with integrated packaging that avoids pollution and increases cuvette utilization.
The Finecare™ TSH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of thyroid stimulating hormone (TSH) in human whole blood, serum or plasma. This test is used as an aid to assist in the assessment of pituitary gland and thyroid function
Finecare™ FIA Meter III Plus is a fluorescence immunochromatographic semi-automatic analysing system with internal temperature control. It can test 20 items at the same time and help diagnose conditions such as infection, diabetes, cardiovascular diseases, renal injury and hormone, etc.
Accre 8 is a compact automatic bench-top Chemiluminescence Immunoassay (CLIA) analyzer. With single-dose reagent cartridge, it allows 600 days MTBF, requiring no extra consumables. It enjoys both simple operation and reliable calibration & quality control system.
Accre 8 is a compact automatic bench-top Chemiluminescence Immunoassay (CLIA) analyzer. With single-dose reagent cartridge, it allows 600 days MTBF, requiring no extra consumables. It enjoys both simple operation and reliable calibration & quality control system.
As one of the world’s smallest, fully automated chemiluminescence immunoassay analyzers, the CL-960i integrates a large capacity and fast assay speed into a compact model, achieving a perfect balance between size and immunoassay testing performance.
ichroma IIA compact and easy-to-use, fluorescence based POCT immunoassay analyzer, Point of care Analyzer ichroma II is a compact, easy-to-use diagnostic immuno-analyzer to measure the presence of various biomarkers for cardiac, cancer, hormones, infectious diseases, autoimmune diseases, and metabolic diseases. iChroma II is an advanced immunoassay reader in our SwifTest range of POC devices. It utilizes the latest immuno-fluorescence technology and provides a simple, fast and reliable method to diagnose a patient’s condition or monitor a treatment response. IChroma II provides results correlating with the laboratory along with all the benefits offered by point-of-care like quick test time, portability, low running costs & user friendly operation making it an ideal choice for any laboratory. IChroma II can be useful for diagnosing conditions such as infection, diabetes, hormonal conditions, cardiovascular diseases, renal injury and cancers etc. in blood, serum, plasma, urine or other samples, in quantitative or semi-quantitative ways.
AFIAS-6Automated Immunoassay Analyzer with the all-in-one cartridge system AFIAS-6 is a unique integrated (sample-to-answer) system featuring 6 parallel tests of differing parameters, fast turn-around and high sensitivity, rivaling those
AFIAS-6Automated Immunoassay Analyzer with the all-in-one cartridge system AFIAS-6 is a unique integrated (sample-to-answer) system featuring 6 parallel tests of differing parameters, fast turn-around and high sensitivity, rivaling those
Detecting the norovirus from the stool sample The active norovirus spreads through contaminated drinking water and related food sources and can cause mass food poisoning. ichromaTM & AFIAS ROTA test can deliver rapid diagnostics in an easy-to-use format even in field clinics to help curtail the spread of the infectious disease.
Even though the Toxoplasma parasite can persist for long periods of time in the bodies, possibly even for a lifetime, healthy people have no symptoms as their immune system usually keeps the parasite from causing illness. However, it could be fatal for pregnant women and individuals who have compromised immune systems. It could cause birth defects or serious health problems. ichroma™ Toxo IgG/IgM can diagnose the point of infection and risk of pregnancy by detecting whether the patient’s immunity was formed.
Non-invasive test to diagnose inflammatory bowel disease (IBD) The elevated level of fecal calprotectin may indicate a case of intestinal inflammation including IBD. This test can tell apart the IBD from the non-inflammatory bowel disease: the level stays low with the latter. It measures the level of fecal calprotectin to help differentiate those seemingly similar diseases.
Assessing to diagnose acute allergic diseases This test assesses IgE in blood to support diagnosing of acute allergic diseases.
Assessing to distinguish and diagnose rheumatoid arthritis This test helps to diagnose rheumatoid arthritis, distinguish it from other types of arthritis and other inflammatory diseases, and ensure proper treatment by rapidly and accurately quantifying RF IgM in blood.
The SARS-CoV-2 virus shares common symptoms with other respiratory diseases. It is contagious even in the asymptomatic stage, which makes it imperative to diagnose the virus early to provide timely treatment and to prevent further transmissions. With its fast turnaround time and high sensitivity, COVID-19 Ag tests would help with the screening program against the COVID-19 pandemic.
COVID-19 virus-specific antibodies are produced when infected with the virus. The presence of this antibody may show the infection in progress or the past infection with active immunity. The COVID-19 Ab test detects the specific antibody to provide information on the patients’ immunity against the SARS-CoV-2 virus. the COVID-19 pandemic.
A high level of CEA in adults can be a sign of certain types of cancers in organs like the colon and rectum, prostate, ovary, lung, thyroid, or liver. The CEA test measures the level of CEA in the patient blood including treatment response and recurrence of cancer patients.
The existence of hemoglobin in stools indicates possible polyps, hemorrhoids, ulcers, and others as well as the colorectal cancer. The iFOB Neo test detects the miniscule amount of blood in the stools. Detection of hemoglobin should warrant further examination.
High levels of AFP in adults may indicate the possibility of the liver, the ovaries, or the testicles, as well as noncancerous liver diseases such as cirrhosis and hepatitis. The AFP plus measures the level of AFP to help diagnose or rule out related abnormalities.
This test helps in the early detection of prostate diseases such as enlarged prostate and prostatitis and prostate cancer by quantifying PSA in male blood, as well as observation of treatment effects and monitoring of recurrence.
.webp)
Tn-I, CK-MB, and Myoglobin are secreted in blood after the heart gets injured by cardiac stress for the lack of oxygen. The levels of these biomarkers can reveal the degree of a heart attack or damage. It would test for the level of those biomarkers in the blood to assist clinicians to assess the cardiac health status.
Troponin I (Tn-I) Plus can diagnose myocardial infarction and myocardial necrosis at an early stage with high sensitivity by accessing Tn-I level in the blood, thus can help prevent progression to more severe cases.
Troponin T is a member of the troponin complex, proteins involved in the contraction of skeletal and heart muscles. It is known as an excellent biomarker to estimate myocardial damage. The Troponin-T test can provide the quantitative result in 12 minutes with fingertip blood.
Helping evaluate the severity of heart disease, including congestive heart failure (CHF) The BNP test the level of BNP in the blood to help assess the severity of heart diseases, including congestive heart failure (CHF).
The appearance of elevated CK-MB levels in serum is highly specific and sensitive for myocardial cell wall injury. Since it varies from one to another, other biomarkers such as Troponin I should be considered together with the CK-MB test to assess heart health. It provides solution to measure blood CK-MB level on a POC level.
Measurement of myoglobin provides an early index of damage to the myocardium, such as occurs in myocardial infarction (MI) or reinfarction. Increased levels, which indicate cardiac muscle injury or death, occur in about 3 hours. Two negative results from consecutive Myoglobin tests eliminate the MI from consideration.
hsCRP is a test for testing the low level of CRP. Significantly high CRP levels are most likely a sign of a serious underlying medical condition. The most common cause is a severe infection, but there are other specific causes leading to a high CRP level. This test measures the level of CRP in 3 minutes.
ST2 signals the presence and severity of adverse cardiac remodeling and tissue fibrosis, which occurs in response to myocardial infarction, acute coronary syndrome, or worsening heart failure. This test provides prognostic information, which is independent of other biomarkers used to probe the cardiac event.
BNP and NTproBNP are peptides that are continuously produced in the heart. When the muscles in the left ventricle over-stretch as in heart failure, the secretion of these peptides into blood increases. One may utilize the level of NTproBNP in blood to assess the cardiac event and its severity. Both of BNP and NTproBNP can be used to show different aspects of the heart failure.
• Efficient recovery of nucleic acids
• Simple extracting steps
• Compatible with various sample types
• Flexible extraction schemes
The Finecare™ Estradiol (E2) Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters is for quantitative measurement of Estradiol (E2) in human whole blood, serum or plasma. The test is used as an aid to the evaluation of ovarian diseases.
The Finecare™ Vitamin D Rapid Quantitative Test along with Finecare™ FIA Meter is a fluorescence immunoassay quantitative determination of total 25(OH) D2/D3 level in human serum or plasma. Results are to be used in conjunction with other clinical and laboratory data to assist the clinician in the assessment of vitamin D sufficiency.
One Step D-Dimer Rapid Quantitative TestThe Finecare™ One Step D-Dimer Rapid Quantitative Test is a screening test with fluorescence immunoassay to be used along with Finecare™ FIA System for quantitative analysis of cross-linked fibrin degradation products containing D-Dimer in human whole blood or plasma. The test is used as an aid in detecting the presence and assessing the degree of intravascular coagulation or thromboembolic events including pulmonary embolism.
The Finecare™ Progesterone Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of progesterone in human serum, plasma or whole blood. The test is used as an aid to the track ovulation.
The Finecare™ fT4 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of free thyroxine (fT4) in human whole blood, serum or plasma. The test is used as an aid to the assessment of thyroid function.
The Finecare™ CEA Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of carcino-embryonic antigen in human whole blood, serum or plasma. The test is used as an aid in the evaluation of therapeutic efficiency, prognosis and recurrence monitoring for carcinoma.
Finecare™ IL-6 Rapid Quantitative TestThe Finecare™ IL-6 Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay for quantitative determination of IL-6 concentration in human venous whole blood, serum or plasma specimen. It is mainly used to monitor the immune status and inflammatory response of the body.
Product DescriptionThe Finecare™ HbA1c Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Hemoglobin A1c in human blood. The test is used as an aid to monitor long-term glycemic status in patients with diabetes mellitus.
The Finecare™ Testosterone Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative measurement of Testosterone in human whole blood, serum or plasma. The test is to be used as an aid in the diagnosis of diseases related to abnormal testosterone levels.
Products: T3, T4, TSH, PSA,FSH, HbA1c,CRP, Vitamin-D,Beta-HCG,Trop-I,D-dimer, PCT (New and advanced Wondfo thyroid function test, through innovative immunofluorescence technique, diagnosing diabetes, cancers and other diseases.)
The Finecare™ CK-MB Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Creatine Kinase-MB (CK-MB) in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of acute myocardial infarction (AMI).
The Finecare™ CK-MB Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Creatine Kinase-MB (CK-MB) in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of acute myocardial infarction (AMI).
The Finecare™ CK-MB Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Creatine Kinase-MB (CK-MB) in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of acute myocardial infarction (AMI).
.webp)
AFP (Alpha Fetal Protein) Rapid Quantitative Test:-The Finecare™ AFP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Alpha-Fetoprotein in human whole blood, serum or plasma. The test is used as an aid for early auxiliary diagnosis and the evaluation of therapeutic efficiency for primary hepatic carcinoma.
The Finecare™ PSA Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative detemination of Prostate Specific Antigen (PSA) in human whole blood, serum or plasma. The test is used as an aid in diagnosis of prostatic cancer.
The Finecare™ One Step cTnT Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay for quantitative determination of cTnT concentration in human venous whole blood, serum or plasma specimen. It is mainly used as an aid to the diagnosis of myocardial infarction.
The Finecare™ T4 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Thyroxine (Total T4) in human whole blood, serum or plasma. The test is used as an aid to the assessment of thyroid function.
The Finecare™ T3 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Triiodothyronine (total T3) in human serum, plasma or whole blood. The test is used as an aid to the assessment of thyroid function.
The Finecare™ T3 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Triiodothyronine (total T3) in human serum, plasma or whole blood. The test is used as an aid to the assessment of thyroid function.
The Finecare™ LH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Luteinizing hormone (LH) in human whole blood, serum or plasma. This test is used as an aid to diagnose the ovulation cycle, premature ovarian failure and gonadal hypoplasia.
The Finecare™ T3 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Triiodothyronine (total T3) in human serum, plasma or whole blood. The test is used as an aid to the assessment of thyroid function.
.webp)
The Finecare™ Prolactin Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative measurement of Prolactin (PRL) in human whole blood, serum or plasma. The test is used as an aid to the evaluation of pituitary endocrine function.
.webp)
The Finecare™ LH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Luteinizing hormone (LH) in human whole blood, serum or plasma. This test is used as an aid to diagnose the ovulation cycle, premature ovarian failure and gonadal hypoplasia.
.webp)
The Finecare™ cTn I Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of cardiac troponin I (cTn I) in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of acute myocardial infarction (AMI).
 - Copy.webp)
The Finecare™ One Step cTn I/CK-MB/Myo Rapid Quantitative Test a fluorescence immunoassay to be used along with Finecare™ FIA System for quantitative determination of cardiac Troponin I (cTn I), MB Isoenzyme of Creatine Kinase (CK-MB) and Myoglobin (Myo) in human whole blood, serum or plasma. The test is used as an aid to the diagnosis of myocardial infarction.
Finecare™ Anti-CCP Rapid Quantitative TestThe Finecare™ Anti-CCP Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay for quantitative measurement of Anti-CCP in human whole blood, serum and plasma. The test is used as an aid in diagnosis of Rheumatoid Arthritis.
.webp)
The Finecare™ Myo Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Myoglobin in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of acute myocardial infarction (AMI).
The Finecare™ One Step MAU Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of urine microalbumin (MAU) in human urine. This test is used as an aid to diagnosis of kidney damage.
.webp)
The Finecare™ Cortisol Rapid Quantitative Test is a fluorescence immunoassay for quantitative determination of Cortisol in human serum, plasma or whole blood. The test is used as an aid to the screening of adrenal dysfunction and assessment of the treatment effect.
The Finecare™ Dengue NS1 Ag Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for qualitative detection of Dengue NS1 antigen in whole blood, serum or plasma specimen. It is useful as an aid in screening of early Dengue virus infection.
Total IgE Rapid Quantitative TestThe Finecare™ Total IgE Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay for quantitative measurement of Total IgE in human whole blood, serum and plasma. The test is used as an aid in diagnosis of allergic disease.
The Finecare™ SAA Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of serum amyloid A (SAA) in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of infection and inflammation.
TSH is the main regulator of thyroid cell growth，thyroid hormone synthesis and secretion. TSH (MW 30 kDa) is synthesized and secreted by tsh cells of pituitary gland, it has negative feedback to the synthesis and secretion process. The fluctuation of TSH is faster and more significant than thyroid hormones when thyroid function was changed, it is a sensitive biomarker of hypothalamic-pituitary-thyroid function.
Tumor Marker Control is intended for performing quality control procedures with MAGLUMI immunoassay (CLIA) reagent kits when used for the quantitative determination of AFP, CEA,CA125, CA15-3, CA19-9, fPSA, tPSA, Ferritin in human serum.
Cardiac Troponin I Fast Test Kit (Immunofluorescence Assay) is intended for in vitro quantitative determination of Cardiac Troponin I (cTnI) in human serum, plasma or whole blood samples. This test is used as an aid in the diagnosis of myocardial injury such as Acute Myocardial Infarction (AMI), Unstable Angina, Acute Myocarditis and Acute Coronary Syndrome (ACS).
Getein hba1c test kit:-HbA1c fast test kit is intended for the quantitative measurement of HbA1c in human whole blood samples. This test is used as an aid for monitoring glycemic control in diabetics. In addition, it can identify people at risk of developing the disease and ongoing monitoring. About HbA1c
The Finecare™ BNP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Brain Natriuretic Peptides (BNP) in human whole blood or plasma. This test is used as an aid to predict the risk of heart failure.
Immunoassay Control is intended for performing quality control procedures with MAGLUMI immunoassay (CLIA) reagent kits when used for the quantitative determination of T3, T4, FT3, FT4, TSH, FSH, LH, PRL, PRG, Estradiol, Testosterone, HCG/B-HCG, Insulin and C-Peptide in human serum.
The TRUSTline Filariasis IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-lymphatic filarial parasites (W. Bancrofti and B. Malayi)in human serum, plasma or whole blood.
STANDARD F HbA1c FIA performs quantitative analysis on glycosylated hemoglobin in whole blood samples using fluorescence immunochromatography. As STANDARD F Analyzer has been enhanced in its performance by using fluorescent substance, accurate quantitative test results can be obtained using with this product.
The Finecare™ 2019-nCoV lgM/lgG Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for qualitative detection of IgG and IgM antibodies of novel coronaviruses (2019-nCoV) in human whole blood, serum and plasma specimen. Clinically, the test is to be used as an aid in the diagnosis of coronavirus infection disease (COVID-19), which is caused by 2019-nCoV.
The Finecare™ NGAL Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Neutrophil Gelatinase-Associated Lipocalin (NGAL) concentration in human urine. The test is used as an aid for the diagnosis of kidney injuries.
Finecare H.pylori Ag Rapid Quantitative Test:-The Finecare™ H.pylori Ag Test along with Finecare™ FIA Meters is a fluorescence immunoassay used for qualitative determination of H. pylori Ag in human feces. The test is used as an aid in the diagnosis of H. pylori infection.
Finecare™ RF Rapid Quantitative TestThe Finecare™ RF Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay for quantitative measurement of RF in human whole blood, serum and plasma. The test is used as an aid in diagnosis of Rheumatoid Arthritis.
The Finecare™ ASO Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay for quantitative measurement of Anti-streptolysin O (ASO) in human whole blood, serum and plasma. The test is used as an aid in the diagnosis of diseases related to streptococcal infections.
Finecare iFOB Rapid Quantitative Test:-The Finecare™ iFOB Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of occult blood in the feces (iFOB). It is suitable for quantitative determination of hemoglobin (Hb) in human feces. Clinically, it is mainly used as an aid for the gastrointestinal bleeding disorders.
The Finecare™ BNP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Brain Natriuretic Peptides (BNP) in human whole blood or plasma. This test is used as an aid to predict the risk of heart failure.
The Finecare™ Lp-PLA2 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Lp-PLA2 in human serum, plasma or whole blood. The test is used as an aid to the assessment of the coronary heart disease (CHD) and ischemic stroke.
Finecare beta2 MG Rapid Quantitative Test:-The Finecare™ β2-MG Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of β2-MG (Beta-2-Microglobulin) concentration in human plasma, serum or whole blood. The test is used as an aid for the diagnosis of renal disease.
The Finecare™ Cys C Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Cys C in human whole blood, serum or plasma. This test is used as an aid to predict the risk of developing chronic kidney disease.
.webp)
The Finecare™ S100β Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of S100β in human serum, plasma or whole blood. The test is used as an aid to the assessment of the level of cerebral injury.
Finecare beta2 MG Rapid Quantitative Test:-The Finecare™ β2-MG Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of β2-MG (Beta-2-Microglobulin) concentration in human plasma, serum or whole blood. The test is used as an aid for the diagnosis of renal disease.
.webp)
The Finecare™ S100β Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of S100β in human serum, plasma or whole blood. The test is used as an aid to the assessment of the level of cerebral injury.
Screening infections in the gastrointestinal tract H. pylori SA is an antigen produced by the immune system to cope with the H.Pylori infection. The level of the antigen examined through the stool serves as a more reliable indicator of the infection than by the one via a blood test, which does not tell if the infection is still active.
The presence of D-dimer in blood indicates that thrombin has been formed and fibrin generated from fibrinogen in vivo as a result of activation of the coagulation system. This test measures the level in the blood to help assess the thrombotic state.
The Finecare™ Ferritin Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of Ferritin in human whole blood, serum or plasma. The test is used as an aid to the assessment of iron deficiency anemia.
For all your Medical Equipment Needs!
