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Covid 19
Antigen Test Kit
Care Start

The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from symptomatic individuals who are suspected of COVID-19 by their healthcare providers.

- RT-PCR Test Kit Manufactured from South Korea
- FDA EUA
- CE
- ISO
- 1 Kit = 100 Tests
- MOQ = 30,000 Tests or 300 Kits
- Price is $11.00 per test or $1,100 per test kit

COVID ANTIGEN TEST -ROCHE
Boxes of 5 tests
Offer: 27 usd (kit with 5 tests)
6000 boxes available

Antigen test kits

Allocation Available
10 Million pcs/month

MOQ : 2.5M Pcs

$5.80 including (CIF Via AIR)

SOP:

ICPO/POF
Commercial Invoice/SPA/POP
SBLC
AWB/SGS/Delivery
SBLC Released

Injection molded from medical grade FHR polypropylene our swab is based on the Harvard Wyss Institute Design and meets the specifications of Health Canada. The swab is also registered with the FDA. Our process allows us to produce approximately 60,000 swabs daily and are ideal for testing or to be included in test kits. The price includes gamma sterilization and individually packaged. Website is www.covidtestswab.com Specifications are as follows:
Overall swab length 149.80 mm
Breakpoint distance from tip 75.75 mm
Swab tip length 20 mm

SARS-CoV-2 Antigen Detection Kit
For Nasal Swab, home testing
Colloidal Gold Method

Package Available: 1 Test/box, 5 Tests/box, 10 Tests/box, 20 Tests/box
Carton Size: 63 x 39 x39cm
Price is different based on QTY from 10K to 500K or above
Payment Term: T/T
Delivery time: 3-5 days
Price Valid: 30 days
Quality Warranty: 2 years.

The COVID-19 IgG/IgM (Whole Blood/Serum/Plasma) Rapid Test Device utilizes lateral flow technology that is used for the qualitative, differential detection of both anti-SARS-CoV-2 IgM and IgG antibodies. In general, antibodies can be detected 1-3 weeks after infection. This test is intended to screen patients for COVID-19. Combining RNA and Antibody tests can significantly raise the sensitivity for detecting COVID-19 in infected individuals.

This test has been authorized by the FDA under a EUA for professional use CLIA and CLIA WAIVED for Point Of Care.
This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens.

This product is intended for professional use and not for home use.

FACT SHEET FOR HEALTHCARE PROVIDERS

This test has been authorized by the FDA under a EUA for use by authorized CLIA laboratories. This device is CLIA waived for point of care use for fingerstick whole blood specimens only. The user should be trained in the procedure. Wear appropriate protective attire for your safety when handling patient samples.
This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens.
There should be a blue line in the control region (next to ) before testing, discard the device if there is no blue line.