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Find Verified Rapid Test Kits Suppliers, Manufacturers and Wholesalers

Top Supplier Cities : -   Chennai   New Delhi  
Jan-26-22
Supplier From Bangalore, Karnataka, India
 
Globally acclaimed Covid Test kits , the best of brands with CE and other requisite certificates are available at a fantastic price ( PanBio/ Flowflex/ Sd Bio sensor) . Delivery all over the globe in 2/ 5 days vide air cargo. We hold the biggest stocks in India. Pl note , prices are quantum based and fluctuate as per demand and supply.
Dec-21-21

Rapid Testing Kits

$100
MOQ: Not Specified
Supplier From Mumbai, Maharashtra, India
 
Rapid testing kits for HIV, HCV, COVID, Malaria, Dengue, HBsAg,
Sep-08-21
Supplier From Pune, Maharashtra, India
 
This is Product is very demand due to pandamic situation. We are supplying ICMR approved ,CE certified product
Sep-08-21
Supplier From Pune, Maharashtra, India
 
We are supplier of ICMR approved ,CE certified test kits for Dengue and Malaria with international standard
Oct-21-21
Supplier From Ghaziabad, Uttar Pradesh, India
 
HCG Test is an immunochromatographic assay designed for qualitative determinatrion of human chronic gonadotropin (hCG) in urine for the detection of pregnancy. Human chorionic gonadotropin is a glycopeptide hormone produced by the placenta during pregnancy. The apprearance and rapid rise in the concentration of hCG in the woman''s urine makes it good pregnancy marker. Usually, concentration of hCG in urine is at least 25mlU/ml within seven to ten days after conception.

Justifying our reputation in this market, we are readily immersed in the arena of offering to our patrons a broad consignment of HCG Tests Kits.

Sensitivity 25 miu



Features:

Precise design

Durable

Good quality
365 Rapid Test Kits Suppliers
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Jul-16-21

Rapid Antibodies Test Kit

$1
MOQ: Not Specified
Supplier From Hyderabad, Telangana, India
 
Rapid Antibody kit used for testing to detect the neutralized Antibodies in Patrons.
Jul-16-21

Rapid Antigen Test Kit

$1
MOQ: Not Specified
Supplier From Hyderabad, Telangana, India
 
Covid19 Antigen testing kit is used for test patrons on Covid19 symptoms.
Feb-23-24
 
A one-step rapid immunochromatographic test for the quantitative detection of specific antibodies to COVID-19 present in human serum, plasma, or whole blood.
Jan-10-24

Rapid Test Kits

$1 - $108
MOQ: Not Specified
 
All types of Rapid test kits
Jun-27-20
Supplier From India
Oct-19-21
Supplier From Ghaziabad, Uttar Pradesh, India
Aug-05-21
Supplier From Surat, Gujarat, India
May-01-25
Supplier From India
Jul-26-20
Supplier From Noida, Uttar Pradesh, India
 
Anti-SARS-CoV-2 Rapid Test, COVID-19
1. Easier: No special equipment needed, Intuitive visual interpretation.
2. Rapid: Quick sampling by fingertip blood, Results in 10-15min.
3. Accurate: Results with IgG and IgM respectively.
4. Application: as screening tool for potential suspect patients in large numbers.

Testing kit is FDA Emergency Use Authorization (EUA) Approved
Testing kit is CE MARKED-IVD

* Instruction for Use
* Interpretation Guide
* SARS-CoV-2 immunoassays
* Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit
* Anti-SARS Rapid Test Brochure
* COVID-19 Catalog
* EUA Approval Letter
* Fact Sheet for Healthcare Providers
* FDA Letter
* Fact Sheet for Recipients
* FAQ
* CE IVD Notification Certificate

Antibody Performance Measure Estimate of Performance 95% Confidence Interval
IgM Sensitivity (PPA) 95.7% (289/302) (92.8%; 97.5%)
IgM Specificity (NPA) 99.7% (311/312) (98.2%; 99.9%)
IgG Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%)
IgG Specificity (NPA) 99.4% (310/312) (97.7%; 99.8%)
Combined Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%)
Combined Specificity (NPA) 99% (309/312) (97.2%; 99.7%)
Combined PPV at prevalence = 5% 84.4% (64.6%; 94.6%)
Combined NPV at prevalence = 5% 99.9% (99.8%; 100%)
Testing kit is FDA Emergency Use Authorization (EUA) Approved
Testing kit is CE MARKED-IVD

* Instruction for Use
* Interpretation Guide
* SARS-CoV-2 immunoassays
* Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit
* Anti-SARS Rapid Test Brochure
* COVID-19 Catalog
* EUA Approval Letter
* Fact Sheet for Healthcare Providers
* FDA Letter
* Fact Sheet for Recipients
* FAQ
* CE IVD Notification Certificate
Oct-10-22
 
Product Details:

Number of Reactions(Preps)/Kit :30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK019-30
STANDARD Q HIV 1/2 Ab 3-Line performs qualitative analysis by detecting antibodies specific to HIV-1 (including Group O) and HIV-2 in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 10 minutes.

Easy to use, Easy to read and interpret
Discrimination between HIV-1 and HIV-2 antibodies
Room temperature storage
Performance
Sensitivity : 100% (74/74)/ Specificity : 100% (232/232)
Jun-09-22
 
A rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2)

Clear, dependable results in 15 minutes

Requires minimal training and no equipment

So easy it can be used at the lowest levels of health care service

Can use whole blood or serum/plasma

Collection can be by fingerstick or venipuncture

No refrigeration required

Storage conditions 2-30�°C
Jun-09-22
 
COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of
Jun-09-22
 
COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
Jun-25-22
 
CAT No : RCHM-02071. The CareStar COVID-19 Antigen test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within first five days of symptom onset, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests.
Apr-24-21
Supplier From Varanasi, Uttar pradesh, India
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