For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing.
1.Easy to collect samples simple operation without professional equipment.
2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy.
4.Suitable for large-scale rapid screening.
Shelf life: 24 Months
Test Result time: 10 Mins
Packing: 25 Pieces per Box
SALESPRICES Antigen Covid-19 Selftest :
DDP US - Home test
1-10M : $7,00/piece
10-50M : $7,00/piece
50m-100m : $6,50/piece
Above 100MM : $6,00/piece
Package: 2 pieces per package
We send you the SOP for the .
1. Standard Operating Procedure
- NCNDA
- LOI
- ICPO
Sales Purchase Agreement
POF (show monies in an account liquid and transactable)
- Delivery Schedule from will be provided.
- Payment 50% full order (date 50% deposit arrives = start production date)
- Seller will provide login on the platform of after SPA signed and down payment, to follow the production of there orders and deliveries directly from Factory.
- 20-25 days: production goods first shipment
- SGS or Equivalent Verification of Product at the factory (client pays)
- Payment 50% first shipment after clients receives SGS (1x/month) or proof of goods video
- Release of goods
- Movement of Product to airport in
- 1-3 days: BOL and Airway Bills
Shipment to the US airport DDP through customs.
Logistics From Airport in US to End Destination included
The correct first delivery we can give after the ICPO. We have capacity in februari for around 500k pieces per day. From : 30 million in a month.
If you want to work with us, dont wait to long because we have a lot of request and just our capacity from our private seller.
Have a nice day
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USA Manufactured, highly accurate, rapid COVID-19 Antigen test. Clinically validated by third-party medical institutions in USA and Europe (Denmark, Poland). The test is highly specific and sensitive (Specificity 100%, Sensitivity 99.1%). Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging.
Manufcatured and ships out of Miami, Florida.
PT Taishan Alkes Indonesia is a pioneering company in indonesia producing Rapid Test Swab Antigen and Rapid Test Antibody to detect the Covid-19 virus.
PT Taishan Alkes Indonesia products are the work of Indonesian people
Our products are made through an effective and efficient production process so as to produce superior quality products according to applicable standards
KFDA & CE approved, FDA Pending
Price : Negotiable
Pre-Clinical Test Report Accuracy - In total samples 93.3% (14/15) - In positive samples 91.7% (11/12)
1. Pre-Clinical Test summary
(1) Pre-clinical test is fulfilled by Domestic large clinical laboratory with ADTech COVID-19 IgM/IgG RAPID KIT
(2) Tests are made by total 15 samples with 12 positive and 3 negative samples
(3) Clinical Laboratory tested the sample with Immunofluorescence Analysis
2. Pre-clinical test result
(1) Samples were tested by ADTech COVID-19 IgM/IgG RAPID KIT
(2) Test result by ADTechs RAPID KIT - 4 negatives and 11 positives results in 15 samples
(3) Comparison between Immunofluorescence analysis and ADTechs RAPID KIT - 14 test results are same(including negative and positive results) - 1 samples test result are different(Positive Negative by ADTech Korea
A rapid test for the qualitative detection of novel coronavirus antigens in nasal, Nasopharyngeal (NP) swab & Oropharyngeal (OP) swab.
The S2 Covid-19 Rapid Antigen Test Kit (swab) is an in vitro diagnostic test for the qualitative detection of novel coronavirus antigens in Nasal swab, Nasopharyngeal swab (NP) and Oropharyngeal swab (OP), using the rapid immunochromatographic method. The identification is based on the monoclonal antibodies specific for the novel coronavirus antigen.
This antigen test is suitable for the qualitative detection of novel coronavirus in Saliva/Sputum/Stool/NP Swab/OP Swab samples (all methods in single test). Result in 15mins
Intended Use:
This product is authorized and intended for use by trained laboratory or healthcare professionals for in vitro diagnostic use. Point-of-care professionals administering tests are required to report all results to the appropriate public health authorities.
Note: Consult your provincial and local health care authorities for POC guidelines for rapid testing use.
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