For in vitro qualitative detection of SARS-CoV-2 nucleocapsid antigen in nasal (NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days after onset of symptoms.
This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, not for at-home testing.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, or 2019-nCoV) is an enveloped non-segmented positive-sense RNA virus. It is the cause of coronavirus disease (COVID-19), which is contagious in humans. SARS-CoV-2 has several structural proteins including spike (S), envelope (E), membrane (M), and nucleocapsid (N).
The antigen is generally detectable in upper respiratory samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but the clinical correlation with patient history and other diagnostic information is necessary to determine infection status.
Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease.
Negative results should be treated as presumptive, which 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. Negative results should be considered in the context of a patient's recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management.
For in vitro diagnostic use only. For professional use only .
Lateral flow assay
No equipment required
Rapid results within 10 minutes
Minimally invasive specimen collection (nasopharyngeal swabs)
POC setting (i.e. in patient care settings) by medical professionals
Detects SARS-CoV-2 nucleocapsid protein antigen with ultra high performance
Identify acute infection wit 88.4% sensitive and 100% specificity
20 test/box
20 test devices
20 assay buffer
20 extraction vials and caps
20 specifimen collection swabs
1 positive and 1 negative control swabs
1 instructions for use
Contents:
Lancet, Pipette, Silica Gel, Alcohol Swab, Test cassette
Number of Kits in a Box:
15 tests
Storage Condition:
Room Temperature
Shipping Type:
Shipping storage condition Room temperature
Analysis Time:
15 Min <
In short:
In the IgG or IgM test line area, it reacts with locally bound anti-human IgG or IgM, respectively and forms a colored line. If sample does not contain any COVID-19 antibodies, a colored line showing a negative result will not appear in any of the Test Line Areas. As a positive check for the correct performance of the tape's procedure and operation, a colored line should always be appearing in the Control Line Area. If Control Line area is empty, then the test is invalid.
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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.
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.
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.
1. Nasopharynx swab specimen, non-invasive
2. Very simple to use
3. Convenient, no devices required
4. Rapid, results within 20 minutes
5. Cost-efficient
6:Listed on German BfArm ,got approval by PEI
Clinical report from local CDC
Sensitivity is 97.14%, Specificity is 100%, total accuracy rate is 99.68%.
We Supple Grade A medical examination Disposable Covid-19 test kit and Syringes with affordable prices in major international market free to contact us for more Quotation.
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.
An established PCR test kit that has had exceptional results both in the lab and in real world settings with major countries reporting sensitivity results. The PCR is the first Korean test kit to receive FDA, EUA, and CE approval, allowing this test kit to be sold globally without restrictions. We are able to secure ample volume reliably.
South Korea-based RapiGEN is a leading manufacturer of in vitro diagnostic industry. The company has developed and manufactured rapid diagnostic test devices for over 15 years. RapiGEN's core raw material, black gold particle, has brought innovation to the in vitro rapid test field with their high specificity, sensitivity, and reproducibility.
Ionebio produces the iLAMP Novel-CoV19 Detection Kit, a real-time Reverse Transcription LAMP-PCR assay system. The test kits are widely used in South Korea, including at ports of entry into the country. Ionebio has secured a facility in the United States which can produce 1 million test per day. This PCR has a 20 minute test time.
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
NAME COVID-19 Nucleic Acid Detection Kit(PCR-fluorescent Probe)
USE Diagnosis COVID-19 rapidly for public disease control
Manual Biological cabinet, Appropriate real time PCR instrument, Appropriate nucleic acid extraction system or kit, Desktop centrifuge ( suitable for 96- well plate or 8-strip tube), Centrifuge with a rotor for 0.2ml reation tubes or plate. Vortex mixer, Adjustable piperres(with maximum capacity of 2 L, 10L, 50L, 100L, and 200L, respectively), Disposible pipette tips with filters, Disposable powder-free gloves, RNase FREE 1.5mL centrifuge tube, PCR reation tube / PCR reaction plate.
Storage and Transportation Store in -20 - 5 and transport with carbon diaxide ice, avoid being repeated freezing and thawing.
Expiration date 9 months
* Please be noted the above is the price including the tax, NOT FOB.
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