Rapid Test Kit QuickVue Infectious Disease Immunoassay Influenza A + B Nasal Swab/Nasopharyngeal Swab/Nasal Wash/Nasal Aspirate Sample 25 Tests CLIA Waived (25/KT)(10 KT/CS) UOM: 25/KT Product number: 20183 Manufacturer: Quidel
Rapid Test Kit Sofia 2 Fluorescence Immunoassay (FIA) Flu + SARS Antigen FIA Nasal Swab Sample 25 Tests UOM: 25/KT Product Number: 20377 Manufacturer: Quidel
Rapid Test Kit Icon 25 hCG Fertility Test hCG Pregnancy Test Serum / Urine Sample 25 Tests CLIA Waived for Urine / CLIA Moderate Complexity for Serum UOM: 100/CS Product Number: 43025A Manufacturer: Hemocue
Rapid Test Kit Icon 20 hCG Fertility Test hCG Pregnancy Test Serum / Urine Sample 25 Tests CLIA Waived for Urine / CLIA Moderate Complexity for Serum UOM: 100/CS Product Number: 395097A Manufacturer: Hemocue
US FDA approved test kit 93.3% sensitivity in confirming COVID-19 cases. Nasopharyngeal test We have OTG and production deals
The COVID-19 IgG/IgM (Whole Blood/Serum/Plasma) Rapid Test Device utilizes lateral flow technology that is used for the qualitative, differential detection of both anti-SARS-CoV-2 IgM and IgG antibodies. In general, antibodies can be detected 1-3 weeks after infection. This test is intended to screen patients for COVID-19. Combining RNA and Antibody tests can significantly raise the sensitivity for detecting COVID-19 in infected individuals. This test has been authorized by the FDA under a EUA for professional use CLIA and CLIA WAIVED for Point Of Care. This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens. This product is intended for professional use and not for home use. FACT SHEET FOR HEALTHCARE PROVIDERS This test has been authorized by the FDA under a EUA for use by authorized CLIA laboratories. This device is CLIA waived for point of care use for fingerstick whole blood specimens only. The user should be trained in the procedure. Wear appropriate protective attire for your safety when handling patient samples. This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens. There should be a blue line in the control region (next to ) before testing, discard the device if there is no blue line.
The kit uses a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) to assay the level of Rat Dehydroepiandrosterone sulfate(DHEAS) in samples. Add Dehydroepiandrosterone sulfate(DHEAS) to monoclonal antibody Enzyme well which is pre-coated with Rat Dehydroepiandrosterone sulfate(DHEAS)monoclonal antibody, incubation; then, add Dehydroepiandrosterone sulfate(DHEAS)antibodies labeled with biotin, and combined with Streptavidin-HRP to form immune complex; then carry out incubation and washing again to remove the uncombined enzyme. Then add Chromogen Solution A, B, the color of the liquid changes into the blue, And at the effect of acid, the color finally becomes yellow. The chroma of color and the concentration of the Rat Dehydroepiandrosterone sulfate(DHEAS) of sample were positively correlated. Standard; 240pg/ml.
1. Generic Name: Novel Coronavirus COVID-19 IgG Antigen Test Kit 2. Brand Name: NIL 3. Notified Category: Other than above substances intended for qualitative determination of COVID-19 infection 4. Class of Medical Device: Class D 5. Shelf life :15 months 6. Sterile/Non-Sterile: Non-Sterilized 7. Contains Drugs: No 8. Medical Device Grouping Category: IVD-Kit 9. Grouping Description: Intended for qualitative determination of COVID-19 infection 10. Intended Use: The Novel Coronavirus COVID-19 IgG Kit is intended for the qualitative detection of human anti-COVID- 19 IgG antibody in human serum/plasma. Any reactive specimen with the Novel Coronavirus COVID-19 IgG Kit must be confirmed with alternative testing method(s). 11. Product Description: Assay controls and 1:10 diluted human serum samples are added to the microtiter wells of a microplate that was coated with COVID-19 recombinant full length recombinant protein. After the first incubation period, the unbound protein matrix is removed with a subsequent washing step. A horseradish peroxidase (HRP) labeled polyclonal goat anti-human IgG tracer antibody is added to each well. After an incubation period, an immunocomplex of "COVID-19 recombinant antigen-human anti-COVID-19 IgG antibody - HRP labeled anti human IgG tracer antibody" is formed if there is specific Coronavirus IgG antibody present in the tested specimen. The unbound tracer antibody is removed by the subsequent washing step. HRP-Labeled tracer antibody bound to the well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the tracer antibody bound to the anti-COVID-19 IgG on the wall of the microtiter well is proportional to the amount of the anti-COVID-19 IgG antibody level in the tested specimen. SALIENT FEATURES: â?¢ Recombinant COVID-19 Spike subunit Protein coated on Microwell Plate â?¢ HRP Conjugated Polyvalent Anti-Human IgG â?¢ Assay Time: 80 mins (30mins+30 Mins+20mins) â?¢ Strip Format Microwell Plate â?¢ Ready to use Substrate and Controls â?¢ Only 20 pL of human serum is required for measurement in duplicate. â?¢ Works on any open ELISA system â?¢ Assay procedure is easy to automate OUR TEST: â?¢ Principle: Indirect ELISA â?¢ The normal healthy patients with samples collected prior to the COVID-19 outbreak [December 3, 2019] (n = 150) and RT-PCR confirmed positive patients in after the second week of the onset of the disease (n = 32). The Positive sample evaluation was done at external Approved Lab. The results are as follows: â?¢ Diagnostic sensitivity is 100% (>98%) â?¢ Diagnostic specificity is 98.67% (>97%) â?¢ PPV: 94.12�°/0 â?¢ NPV: 100% Please contact us for more information and product details.
Clinitest OTC covid test kits (by Siemens) - FDA approved for use in the USA - Capacity to supply 5M per week - 50% payment up front, then the remaining 50% after the airway bill and packing slip are provided
Covid 19 Rapid Antigen Test Kits Brand: Healgen Scientific Antigen Protein Swab Rapid Test 96% Accurate 15 Minute Response
First Aid Kits: Home FAK,Car FAK,Bike FAK,Office FAK,Pet FAK Different types of packaged kits, such as pouches, plastic case, metal case, etc. Different FAk with different components: Adhesive strips, cohesive bandage, gloves, gauze pad, cleaning wipes,scissors,tweezers,alcohol pads, survival rescue blanket ,adhesive tapes,triangular bandages. etc.
First Aid Kits: Home FAK,Car FAK,Bike FAK,Office FAK,Pet FAK Different types of packaged kits, such as pouches, plastic case, metal case, etc. Different FAk with different components: Adhesive strips, cohesive bandage, gloves, gauze pad, cleaning wipes,scissors,tweezers,alcohol pads, survival rescue blanket ,adhesive tapes,triangular bandages. etc.
Free shipping, 1 Pallet MOQ 1,152 tests per pallet.
IV Kit Includes Tegaderm 2.375 2 3/4 2 2 4-Ply NW Gauze Chloraprep Sepp, Transport Tape Roll 24 Tourniquet Change Label, 100kit/cs UOM: 100/CS Product Number: 69244 Manufacturer: Medical Action Industries
Access Bio Covid 19 Antigen Test Kit Care Start The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from symptomatic individuals who are suspected of COVID-19 by their healthcare providers.
BinaxNOW COVID-19 Antigen Self Test (2 tests for serial testing) A simple solution for COVID-19 infection detection, with rapid results. This test has received FDA Emergency Use Authorization for self-testing without the need to ship samples to a lab or for a prescription from your healthcare provider. This 15-minute test can be completed anytime, anywhere. Simply test yourself twice within 3 days, with at least 36 hours between tests. MOQ 50,000 Worldwide Shipping
Health Canada Authorised Rapid Test The COVID-19 antigen rapid test device is a lateral flow in-vitro immunoassay intended to be used for the qualitative detection of the SARS-CoV-2 viral nucleoprotein. This device will detect both viable and nonviable virus in both nasopharyngeal and oropharyngeal secretions. This test had been authorized for point of care use by Health Canada and is available for immediate dispatch MediGuard Systems of Canada is an Authorised distributor of the Assuretech Rapid Antigen test. Support documentation and details available on request
Rapid Test Kit Sofia RSV FIA Fluorescence Immunoassay (FIA) Respiratory Syncytial Virus Test (RSV) Nasopharyngeal Swab / Nasopharyngeal Wash / Nasopharyngeal Aspirate Sample 25 Tests CLIA Waived UOM: 25/KT Product Number: 20260 Manufacturer: Quidel
Rapid Test Kit Sofia Fluorescence Immunoassay (FIA) SARS Antigen FIA Nasal Swab / Nasopharyngeal Swab Sample 25 Tests UOM: 25/KT Product Number: 20374 Manufacturer: Quidel
Molecular Diagnostic / RT-PCR Quality Control Kit Cobas Liat SARS-CoV-2 and Influenza A / B Positive Level / Negative Level 3 X 0.25 mL / 3 X 10 µL / 3 X 0.3 mL UOM: 1/KT Product Number: 09211128190 Manufacturer: Roche
