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
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
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.
The performance of SARS-CoV-2 Antigen Rapid Test NOTE:Sign a contract with the distributor. If you want to sign a contract with the factory, please don't ask, Payment method : escrow bank,LC(Less than $350000ï¼? Welcome real buyers,Orders can be tested in small batches
A serology test or Antibody Rapid Test which doesn't test for the virus itself. Instead, it look for body's immune response to the virus. This test is getting popular is not only because its convenience but also because it can identify whether youâ??ve ever been exposed to SARS-CoV-2 - which would deepen our understanding of who is getting sick, particularly people who showed few or no symptoms. It could also allow people whose bodies seem to have some degree of immunity to the illness to return to work more quickly. Please email us and get detailed factsheet, certification etc.
GOLD STANDARD for diagnosis novel coronavirus. This kit is based on one-step RT-PCR technique. Used for the in vitro qualitative detection of novel coronavirus (2019-nCoV) ORF1ab and N gene in the throat swabs, sputum specimens of suspected pneumonia patients infected by novel coronavirus, suspected clustering cases and others needing diagnosis or differential diagnosis for novel coronavirus. No cross-reaction, sensitivity is 500 copies/ml. CFDA/CE. Applicable Instruments include ABI 7500 & LightCycler480.
2019-nCoV Neutralizing Antibody Test Kit Fluorescence Immunochromatography (Serum/plasma) Rapid Test: Just for 15 Minutes Accurate Result: Fluorescence immunoassay, high sensitivity Convenient operation with smart POCT analyzers Rate COVID-19 Vaccine immediately Application By testing neutralizing antibody titer after COVID-19 Vaccination, it will be able to figure out the vaccine efficiency Product Information Product Name: 2019-nCoV Neutralizing Antibody Determination Kit Methodology:Fluorescence immunoassay Size:25 Tests/box Storage and Validity:Stored at 2-30 within 18 months Specimen:-Clinical fresh human serum, recommended EDTA anticoagulant plasma Easy Operation: 1 Take 100 sample to buffer and mix 5-10s 2 Add 80 mixed sample to strip 3 Incubation time: 15 mins 4 Put strip into analyzer to test
The PocRoc SARS-CoV-2 Neutralizing Antibody Rapid Test Kit is developed for in vitro qualitative detection of SARS-CoV-2 neutralizing antibodies in human serum, plasma, or whole blood samples. SARS-CoV-2 Neutralizing antibody is an important marker for assessing the effectiveness of the SARS-CoV-2 vaccines. The reagent is for neutralizing antibody detection in samples from individuals after vaccine injection or recovered from COVID-19. PocRoc�® SARS-CoV-2 Neutralizing Antibody Rapid Test Kit has great significance for the development of SARS-CoV-2 vaccines, evaluation of effectiveness, and evaluation of neutralizing antibody levels in human bodies. For Medical Professional Use Only! TEST PROCEDURE Do not open the sealing strip until you are ready to perform a test, and the single-use test is suggested to be used under a low environment humidity (RHâ?¤70%) within 1 hour. 1. Allow all the components of the kit and specimens to reach room temperature prior to testing. 2. Take out the test card and place it on a clean dry surface. 3. Identify the test card for each specimen. 4. Use a dropper to deliver one drop (~40�¼l) of serum, plasma, or whole blood samples into the sample well on the test card, followed by one drop (~40l) of sample buffer. 5. Start the timer and read the result immediately after 15 minutes, and the result after 30 minutes is invalid.
#b2b #Manufacturer #Exporter #COVID-19 #Stock #Antigen rapid test kit #anti-epidemic Provide high-quality products at competitive prices Product: SARS-CoV-2 Antigen Rapid Test Kit Standard: CE, FDA certification Packing quantity: 25tests/box FOB: US$1.60/test
*High reliability and accuracy *Rapid test *Easy and safe to use *Made in korea
*Rapid test kit. *Easy and safe to use. *High reliability and accuracy *Made in korea
It's special designed to detect the Beta-lactam,Tetracyclines in raw, commingled cow milk at or below established tolerance and/or safe levels. The kit is only for screening test, positive result should be further confirmed with other method.
It's special designed to detect the Beta-lactam,Tetracyclines, Sulfonamides, Chloramphenicol in raw, commingled cow milk at or below established tolerance and/or safe levels. The kit is only for screening test, positive result should be further confirmed with other method.
Information Detail Test time Within 15 mins Specimen Whole blood/Serum/plasma Storage temperature 2-30/36-86 The BIOGENIX COVID-19 Rapid Test Kit is a qualitative lateral flow immunochromatographic assay for the detection of IgM and IgG antibodies to SARS-CoVID-19 in human whole blood, serum or plasma samples. It is intended for use as a tool to assist in the diagnosis of SARS-CoVID-19 infections. It is also intended as a tool for carrying out serological epidemiological investigations.
Covid Rapid Test, CE and CFDA certified, export licenses and local Chinese authorities approval.
2019 nCOV Detection Kit (2019-nCoV) IgG/IgM� Rapid Test kit Approved by FDA LineGene K Plus Real-Time PCR Detection System Model FQD-48A
Covid-19 Rapid Test kit(IgG/IgM) - Made in USA (Its made in USA product with Korean technology) - Product will be dispatched from USA. - Package : 25 Tests/Kit - Price : FOB USA(New Jersey), USD 13/test - MOQ : 100,000 test - Lead time : immediately (In stock) - USA FDA EUA approved - CE approved
It's special designed to detect the Beta-lactam,Tetracyclines, Sulfonamides in raw, commingled cow milk at or below established tolerance and/or safe levels. The kit is only for screening test, positive result should be further confirmed with other method.
HCV Rapid Hepatitis C Virus Test (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibody to Hepatitis C Virus in whole blood, serum or plasma. It is for professional in vitro diagnostic use only
The HIV 1/2 Ab Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay with a double antigen system for the qualitative detection of antibodies to HIV-1 and/or HIV-2 in whole blood, serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with HIV. Any reactive specimen with the HIV 1/2 Ab Rapid Test Cassette must be confirmed with alternative testing method(s).
