Genbody Influenza/ Covid - 19 Ag Triple, Rapid immuno-diagnosis of influenza A, B & SARS-CoV Single test for 3 parameters: antigen test of influenza A,B & SARS-CoV-2 Easy to use, Simple Procedure, Quick resulting and high Accuracy. Production information: 1.Specimen: nasopharyngeal swab or Viral transport medium (VTM) 2.No Cross-reaction with 27 kinds of other respiratory viruses. 3.No interference with 23 kinds of interfering substances. 4.Limit of detection (LoD):1.89x10 HA units/mL for influenza A, 4.1 x 10 HA units/ mL for influenza B, 1.78x10 TCID/mL for SARS-CoV-2. 5.Detection of SARS-CoV-2 Varients: alpha,beta,gamma, delta, omicron & stealth omicron.
Cat No: RK056-20. STANDARD Q COVID-19 IgM/IgG Combois a rapid Immunochromatographic assay for the qualitative dtection of specific antibodies to SARS-CoV-2 present in human Serum,Plasma or Whole Blood specimen. Rapid testing for detection of IgM & IgG antibodies against SARS CoV-2 10 µl of specimen: Serum, Plasma & Whole Blood Long term storage of 24 months at 2 - 30 C Complementary to RT-PCR Test Can be performed without extra equipment
Cat No: 41FK10. Panbio COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of SARS-CoV-2 antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. Panbio COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of SARS-CoV-2 infection.
Cat. No : 5513C. 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 : F-NCOV-01G. STANDARD F COVID-19 Ag FIA is the fl uorescent immunoassay for the qualitative detection of specific nucleoprotein antigens to SARS-CoV-2 present in human nasopharynx. STANDARD F COVID-19 Ag FIA should be used with the STANDARD F Analyzers manufactured by SD BIOSENSOR. This test is for in vitro professional diagnostic use and intended as an aid to early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection.
The iFinDx COVID-19 IgM/IgG is a rapid test kit for differential detection of specific IgM and IgG against COVID-19 in human serum, plasma and whole blood.
Product Details: Brand : ABBOTT ICMR Approved : Yes Result Time (Rapid Kits) : 10-15 mins Packaging Size: 1 T CAT No : 41FK51 Certified CE certified The Panbio COVID-19 Antigen Self-Test is a single-use, in vitro (outside the body) visually read rapid immunoassay that uses a human nasal swab specimen for the qualitative detection of nucleocapsid protein SARS-CoV-2 antigen. The test can determine if you have an active COVID-19 infection and you will know your test results in just 15 minutes Only Proven High-Accuracy Self-Test in India In clinical evaluations with self-test users, the Panbio COVID-19 Antigen Self-Test correctly identified 100% of negative samples and 95.2% of Positive Samples Pregnancy had no impact on the performance of the test.
Product Details: Brand : Premier medicals Result Time (Rapid Kits) : 15 min Sample Type : Nasal Swab Packaging Size : 25 Test Kits/Box CAT No : SS03P25 Certified WHO Approved Sure Status COVID-19 Antigen Card Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx
Product Details: Number of Reactions(Preps)/Kit ; 2 Brand ; Genbody Test Method : Antigen Test Result Time (Rapid Kits) : 10-15 mins Certified : CE certified Cat. No : COVAG025-1 The GenBody COVID-19 Ag is an immunochromatographic rapid diagnostic test (RDT) intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) oranteriornasal (AN) swab specimens from individuals who are suspected of COVID-19 by their healthcare provider within the first six days of symptom onset
- EXW $8.5 (in USA)/test (2 test kits/1 inbox) - Non-Prescription Home Test Kit (Individual Use). - Result in 15 min. - FDA (EUA), CE approved. - Supply from authorized Distributor in the USA - Gaurantee that our price is cheaper than other suppliers - Celltrion supplies their antigen to the US Department of Defense -> PROVED QUALITY
Quantity: 250,000 (250K) Lyher - 1 tests per package - price ¬ 1.70 officially approved by the BfArM test suitable for lay use rapid sampling through the nose user-friendly step-by-step instructions Test result within 15 minutes LYHER Novel Coronavirus (COVID-19) Antigen Test Kit (Colloidal Gold) from the manufacturer Hangzhou Laihe Biotech Co., Ltd., China If interested, just let us know Quantity: 250.000 (250K) Lyher â?? 1 tests per package â?? Preis â?¬1,70 offiziell durch das BfArM zugelassener Test geeignet f�¼r Laienanwendungen schnelle Probenentnahme durch die Nase benutzerfreundliche Schritt-f�¼r-Schritt-Anleitung Testergebnis innerhalb von 15 Minuten LYHER Novel Coronavirus (COVID-19) Antigen Test Kit (Colloidal Gold) des Herstellers Hangzhou Laihe Biotech Co., Ltd., China
1.7 Mill pieces LEPU - Covid quick test 1,04 USD ;0.88,- Euro ; OTG Eu
SARS-CoV-2 Test Kit made in Korea: - Target Gene: Orf-1ab gene & E-gene - Performance: Sensitivity: 77 genome copy equivalents/rxn - Running time:
[ZENITH GROUP] COVID-19 Test Kit o Product Name - PCL COVID-19 AG Test Kit(Salvia) - PCL COVID-19 lgG/lgM o Price (USD) : 3.2$ (FOB) - Can be discussed up to order Qty - 10,000 : 3.2$ - 100,000 : 3.0$ - 1,000,000 : 2.8$ o MOQ : 10,000 pcs o Payment : 100% L/C at sight, irrevocable, transferable LC o Delivery Time- Up to Qty- Capacity : 3,000,000pcs / 1week
This device is a qualitative serology test based on immunochromatography. The appearance of a coloured band indicates the presence of the antibody within 10 minutes. The test can be used for vaccination control. This test controls two types of antibodies in parallel: IgM and IgG. The IgM antibody level starts to be truly detectable about a week after the initial infection, while IgG usually appears within 14 days of infection and can last for several months or even years. The device is now approved by the Ministry of Health. Using two drops of blood, the test can detect COVID-19 in less than 10 minutes. The test is based on the detection of antibodies specific to the disease. The test has the advantage of giving a result during and after contamination. The specificity of the test (IgM and IgG) is 100% (study carried out by different hospitals). The sensitivity of the test is 92.8% for IgM antibodies and 96.5% for IgG antibodies for false negatives (1300 tests). The performance values of our device are in line with the recommendations of the Haute Autorit de Sant (HAS) The test have been approved and controlled by French government (ANR: Pasteur)
covid tests
PRICE PER TEST $8.99 TEST BinaxNOW COVID-19 Ag Card For Rapid Detection of SARS-CoV-2 | FDA EUA | IVD Use | RX Only The BinaxNOW COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset. Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen. Antigen is generally detectable in anterior nasal (nares) swabs during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Negative results should be treated as presumptive, do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. The BinaxNOW COVID-19 Ag Card is intended for use by medical professionals or trained operators who are proficient in performing rapid lateral flow tests. BinaxNOW COVID-19 Ag Card is only for use under the Food and Drug Administration's EUA. Kit Details Test Card: 40 cards with test strips Extraction Reagent: bottle containing 7.5 mL of extraction reagent Nasal swabs: 40 sterile, single use specimen sampling swabs Positive Control Swab: 1 each â??individually wrapped for single use Negative Control Swab: 1 each â??individually wrapped for single use Documentation: Product Insert, Procedure Card Performance Data Sensitivity: 97.1% Specificity: 98.5%
US FDA approved test kit 93.3% sensitivity in confirming COVID-19 cases. Nasopharyngeal test We have OTG and production deals
We are a manufacturer of SARS-CoV2 (Covie-19) antigen RAPID TEST CASSETTE. The Genesea SARS-CoV-2 Antigen Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection the antigen from SARS-CoV-2 in nasal swab, nasopharyngeal swab, oropharyngeal swab specimens. The products have CE certification, We can provide you at cheapst price. Delivery time 5days. Capacity 10million tests/month
DEAR, LIVE STOCK BELGIUM MOQ : 500 PRICE : 2,5â?¬/ TEST + delivery cost 1 pack First come, First served