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Find Verified Diagnostic Kits Suppliers, Manufacturers and Wholesalers

Aug-10-22
Supplier From Hangzhou, Zhejiang, Hong Kong
May-23-22
Supplier From Seongsu, Seoul, South Korea (Republic Of Korea)
May-30-18
Supplier From Vung Tau, Baria-Vung Tau, Viet Nam
Mar-15-22
Supplier From Nantong, Jiangsu, China
Mar-18-24
Supplier From China
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Feb-02-24
Supplier From Delhi, Delhi, India
Oct-23-23
Supplier From India
Dec-20-23
Supplier From China
Sep-06-23
Supplier From Shenzhen, Guangdong, China
Jul-21-23
Supplier From Vadodara, Gujarat, India
May-18-23
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Apr-28-23
Supplier From Qingdao, China
Apr-19-23
Jul-20-22

Covid 19 Rapid Antigen Test

$1.90
MOQ: Not Specified
Supplier From Kuala Lumpur, , Malaysia
 
The HY-T COVID-19 Antigen Self-Test (Nasal Swab) is lateral flow assay designed for the qualitative detection of specific SARS-CoV-2 antigen in human anterior nasal swab specimen. It is intended to be used for the detection of SARS-CoV-2 virus infection. The results obtained should not be the sole determinant for clinical decision. The HY-T COVID-19 Antigen Self-Test (Nasal Swab) is intended for use for home self-testing.

Platform: Immunochromatographic Assay
Format: Cassette
Detection Specific: SARS-CoV-2 antigen
Specimen: Nasal swab
Sensitivity: * 97.17%
Specificity: * 100%
Assay Time: 15-20 minutes
Shelf Life: 18 months

* Vs FDA Emergency Use Authorized real-time RT-PCR
Suitable for:

Individuals who wish to know their status on COVID-19 infection (symptomatic and asymptomatic regardless of their vaccination status)Individuals who have had close contact with COVID-19 positive patientsIndividuals with suspected exposure to coronavirusIndividuals who show symptoms related to COVID-19 (fever, dry cough, tiredness, sore throat,headache etc)Employees to perform regular testing to avoid workplace transmission Other appropriate and necessary screenings (such as International Entrance, cross-state, pre-employment screening, pre-admission to higher learning institutions etc.
Mar-21-24
 
Various formats are available, and OEM and ODM customization is accepted.
Mar-21-24

Malaria Rapid Test

$0.25
MOQ: Not Specified
 
A variety of malaria tests are available, including the Malaria Pf/Pv Test Malaria Pf/Pan Test Malaria Pf Test and Malaria Pan Test
Jan-16-23
Supplier From Gyeonggi, Republic Of Korea, South Korea (Republic Of Korea)
 
It is a kit that can easily self-check Covid-19. It has an affordable price and high diagnostic accuracy.
- Excellent accuracy and fast reading
- Optimized for self-examination with easy and easy procedures
- Two-color result display using Nano Band for easy reading
- Use nasal swab samples
Aug-25-23
 
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.

EUA and CE pass
shelf life: 24months since manufacturing date
packing:2pcs/box,4pcs/box and so on

It is for self testing and OTC, for home use, school , and any group .
Aug-25-23
 
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.
View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
Aug-25-23
 
The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.
View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.
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