The iNSTAXPLOR COVID-19 Ag is a rapid chromatographic immunoassay for the qualitative detection of antigens specific to SARS-CoV-2 in swab samples collected from a human nasopharynx. SALIENT FEATURES -Best suited for early detection of COVID â?? 19 infection from the onset of symptoms -Point-of-care test / On the spot test -Quick results in 15 to 30 mins -ICMR validated and approved -No Equipment required - All Material provided in the Kit to perform the test -Recommended for administration by qualified healthcare workers -Storage at Room Temperature (2-30C). -Shelf life: 24 months
Catalog Number: FRT02 Type: FAMEX SARS-CoV-2 Saliva Antigen Rapid Test Kit Technical: Rapid Antigen Test Kit Specimen Types: Sputum Claim: Sensitivity .4 Specifity ,3 Contents: Pipette, Test Cassette, Specimen Tube, Medical Waste Bag, Silica Gel Storage: 2 C -30 C Shipment Type: 2 C -3 C Analysis Time: 15 Minutes Shortly : This kit is used for the qualitative detection of SARS-CoV-2 antigen in vitro environment. It is a lateral flow sandwich assay designed for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 directly in saliva.Packaging, package leaflet and manual customized for various markets.
Catalog Number: FRTFT02 Type: FAMEX SARS-CoV-2 NASOPHARYNGEAL AG RAPID TEST KIT Technical: Rapid Antigen Test Kit Specimen Types: Nasopharyngeal Swab Claim: Sensitivity .7- Specifity .06 Contents: Swab, Test Cassette, Specimen Tube, Medical Waste Bag,Silica Gel Storage: 2C - 30 C Shipment Type: 2 C- 30 C Analysis Time: 15 Minutes Shortly: This kit is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 Nucleocapsid Protein in Nasopharyngeal Swab as an aid in the scientific research of primary and secondary COVID- 19 infections.Packaging, package leaflet and manual customized for various markets.
We are supplying FDA's EUA approved Covid 19 Test Kit to the US. Our COVID-19 Detection Kit is a real-time PCR based in-vitro diagnostic product intended for detection of the novel coronavirus SARS-CoV-2 (COVID-19) RNA in sputum, bronchoalveolar lavage, oropharyngeal or nasopharyngeal smears collected from patients with suspect viral infection The kit is composed of Internal Positive Control (IPC), to monitor appropriate performance of amplification and detection of the kit. Accurate detection of the viral RNA is confirmed parallelly by using Positive and Negative controls which are composed in the kit
nasal or throat swab, 25 tests per box, it has CE certificate
Russia and non russia oil and gas (kazakhstan, qatar, netherlands) oil and gas products such as en590 10ppm, d6, jet fuel a1 & 54, lng, lco, ago, d2, espo, pet coke, sulphur, urea 46 granular/prilled and others. in addtion, nitrile gloves, face mask, covid testing kits, and other ppe products to overseas including the usa & europe & other countries..
[ZENITH GROUP] COVID-19 Test Kit o Product Name - Gendbody COVID-19 AG Test Kit - Gendbody COVID-19 AG Home Test Kit - Gendbody COVID-19 lgG/lgM o Price (USD) : 2.5$ (FOB) - Can be discussed up to order Qty - CIF : Can be discussed o Certification : CE,FDA o MOQ : 1,000 pcs o Payment : L/C, TT o Delivery Time - Up to Qty - Capacity : 3,000,000pcs / 1week Genbody Covid-19 AG Home Test Kit is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein from SARS-COV-2 from individual's nasal specimen with or without COVID-19 symptoms.
Direct to the seller side Covid-19 Rapid Antibody, Antigen Test Kits Covid-19 Vaccine -> Currently actively working with many govt bodies experiencing Massive success. after my own dd & NCNDA, will link you up directly to the sell side. this is as close as you can get to the end seller for this sort of commodity. Contact me for more information. There are however, a very high demand and I experience high volumes of enquiries daily and i do not wish to waste anyone time. Looking for a sincere long term working relationship/partnership. so any circumventing, funny business will not be tolerated.
CAT No : RK055-25. STANDARD Q COVID-19 Ag is a rapid Immunochromatographic assay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx. Qualitatively detects specific antigens to SARS-CoV-2 present in Human Nasopharynx. The test should be used as an aid in early diagnosis of symptomatic cases in healthcare setting having ILI. Validated by ICMR & AIIMS Sensitivity of 84.38 % & Specificity of 100% Sample Type- Human Nasopharyngeal swab (No other sample recommended) Results in 15-30 mins
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
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit(Colloidal Gold)is used for qualitative detection of SARS-CoV-2 virus nucleocapsid protein, which is an important conserved structural protein of SARS-CoV-2 in human nasal/ oropharyngeal samples. The detection of SARS-CoV-2 nucleocapsid protein antigen can be used to assist the diagnosis of novel coronavirus infection and is helpful for the early detection of novel coronavirus pneumonia infection in the latent period.
Both COVID-19 and influenza A/B viruses (Flu A/B) can cause acute respiratory infections, and people are generally susceptible. These three viruses are highly contagious, spread quickly, have a short incubation period, and have a high incidence. Symptoms of COVID-19 and influenza may look similar; the main symptoms include fever, dry cough, fatigue, etc. With this combination test, healthcare workers can provide an accurate diagnosis to patients and treat them with the appropriate measures. Feature Results ready in 15 minutes Accurate diagnostic tool for active infection Easy to administer and read results Affordable, no need for instrument, highly portable Enable testing on a massive scale For healthcare workers use only
To help stop the spread of COVID-19, Singclean Medical has developed COVID-19 Antigen Test Kits saliva swab which is a solid phase immunochromatographic assay for the rapid, qualitative detection of antigen from COVID-19 in human saliva swab specimen. The test provides only a preliminary test result. Therefore, any reactive specimen with the COVID-19 Antigen Test kit (Colloidal Gold) must be confirmed with alternative testing method (s) and clinical findings. Advantage: Quick: results ready in 15 minutes Affordable: no need for instrument Accurate diagnostic tool for active infection Easy to administer and read results Enable testing on a massive scale Non-invasive: more comfortable than nasopharyngeal swab Warnings 1. Use fresh samples whenever possible. 2. Positive results do not rule out bacterial infection or co-infection with other viruses. 3. A negative result can occur if the quantity of the COVID-19 antigen present in the specimen is below the detection limits of the assay, or failed to collect the COVID-19 antigen. 4. Negative results do not rule out infection with COVID-19 and should not be used as the final or sole basis for treatment or patient management decisions. Negative results should be considered in the context of a patientâ??s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19. For a more accurate test result, repeat the tests or confirmed with other testing methods and clinical findings is recommended
CE Approved Covid-19 IgG/IgM Antibody Blood Test Kit can be used as an initial screening for qualitative and differential detection. Throughout testing the antibody of IgG and IgM immunoglobulins in human serum, plasma or blood, the test kit can show the result in a short time. Relative sensitivity 96.00%(192/200) Relative specificity 98.29%(806/820) Accuracy 97.84% (998/1020) Advantages Fast detection: 10 minutes to interpret the result; Easy to operate: no complex equipment required during test; Sensitive: the product has a higher sensitivity than PCR Nucleic Acid Global Network Singclean@COVID-19 lgG/gM Test Kit has been sold to more than 50 countries in the worid, like Brazil, Chie,Polandï¼?spain, Bolivia, Greece, Lihuania, Ecuador, Ukraine and Turkey. Precaution It is worth noting that the result of Covid-19 IgG/IgM antibody blood test should not be used as the only evidence of Coronavirus diagnosis. Professional doctors and clinical findings are necessary if the result of antibody test is positive. Besides, the test kit should be operated by professionals only. Use by individuals may cause deviation in test results. Limitation False negative and false positive could happen. If the antibody is lower than the detection level, especially in the 7 days of the onset of symptoms, a positive patient may also be diagnosed as negative.
CE Approved Singclean COVID-19Test Kit (Colloidal Gold Method) is a solid phase immunochromatographic assay for the rapid,qualitative detection of antigen from COVID-19 in human nasal swab specimen.This test provides only a preliminarytest result. Therefore, any reactive specimen with the COVID-19 Test Kit (Colloidal Gold Method) must be confimed with alternative testing method(s) and clinical findings. This rapid antigen test kit is the second test kit developed by Singclean Medical for COVID-19 testing on the basis of Colloidal Gold Method after Singclean COVID-19 lgG/IgM Test Kit, an antibody test, was launched globally in March. Advantage Results ready in 15 minutes Accurate diagnostic tool for active infection Easy to administer and read results Affordable, no need for instrument, highly portable Enable testing on a massive scale For healthcare workers use only Sensitivity 98.56% Sensitivity 99.03% Accuracy 98.84% Warnings 1. This test is not for at home testing, and should only be operated by healthcare workers. 2. Optimal assay performance requires strict adherence to the assay procedure described in this insert sheet. Inadequate or inappropriate sample collection, storage, and transport may cause false test results.
Hello,Sir Or Madam! Good News For You! I'm Tony Tsui, The Executive Of Runway Group. We Runway Group have successfully R&D the New Very Hot Hot Hot Product :COVID-19 Antibody Rapid Test kits .This Has been used and inspected by many hospitals In Wuhan And China Other Cities ,Now,our test kit FDA&CE Approved Certificates,it can sell all the world. It Is very hot product For many countries ,many governments ,many Hospitals for all the World! Now We Wanted The Exclusive Agent In Your Country in all the world! CIFCustomer Country Unit Price :xx Usd/pcs ,MOQ:0.2million Pcs ,3-5 working days shipment. When We Received 100% Prepayment By T/T or L/C AT SIGHT.
Rapid SAR-CoV-2 (Covid-19) Test Kits: FDA & CE Approved (Results in 15 min). SAR-CoV-2 IgG/IgM Rapid Test Cassette is a qualitative membrane based immunoassay for the detection of IgG and IgM antibodies to SAR-CoV-2 in human whole blood, serum or plasma specimen. Made in China: FDA and CE Approved, China NMPA approval (export allowed) One of the earliest CE (Feb 2020) and FDA (Mar 2020) approved kit. Clinically studied and reliable. Packaging: 20 sets/box or 40 sets/box. Payment term: MOQ 2000 sets, FOB China $ 9.5/set. < 10000 sets 100% advance payment > 10000 sets L/C ex-work on site
Catalog Number: FRT01 Type: FAMEX Coronavirus (2019-nCoV)-Antigentest Technical: Rapid Antigen Test Kit Specimen Types: Nasal Swab Claim: Sensitivity .7 Specifity Contents: Swab, Test Cassette, Specimen Tube, Medical Waste Bag,Silica Gel Number of Test: Disposable Storage: 2C 30 C Shipment Type: 2�°C â?? 30�°C Analysis Time: 15 Minutes Shortly: This kit is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 Nucleocapsid Protein in nasal swab as an aid in the scientific research of primary and secondary COVID- 19 infections.Packaging, package leaflet and manual customized for various markets.
Joysbio Saliva Rapid Test Kit - Saliva Test Kit for public use / under 30 minutes / Sensitivity 95.10% / TCID50 320 / CE IVD marked for public use / In stock in Germany
For the qualitative assessment of COVID-19(SARS-CoV-2) neutralizing antibody after the vaccination in human serum/plasma/whole blood. Sensitivity: 95.39% Specificity: >99.9% Accuracy: 98.47% CE Certificate available.
