The CareStart COVID-19 Antigen test kit allows for the rapid screening of COVID-19 infection on a large scale, with results in just 10 minutes. 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 individuals who are suspected of COVID-19 by their healthcare providers. This product is CLIA waived under FDA/EUA authorization.
Quantity: 8 Million test kits
MOQ: 1 Million
FOB: New Jersey USA
Price: 11.75 USD
Intended Use:
This product is authorized and intended for use by trained laboratory or healthcare professionals for in vitro diagnostic use. Point-of-care professionals administering tests are required to report all results to the appropriate public health authorities.
Note: Consult your provincial and local health care authorities for POC guidelines for rapid testing use.
Made in Canada
Health Canada approved
CE Mark and ISO certified
The product has proven to have 100% Specificity and 96% Sensitivety
Stock availabity: 2 Million tests/kit in Canada
Production: up to 5 Million tests/kit weekly
The Rapid Response COVID-19 Antigen Rapid Test Device is an in vitro immunochromatographic assay for the direct and qualitative detection of SARS-CoV-2 viral nucleoprotein antigens from nasal and nasopharyngeal secretions from individuals suspected of COVID-19 within 6 days of symptom onset. This test is authorized for use at the Point of Care i.e., in patient care setting. Results are for the identification of SARS-CoV-2 viral nucleoprotein antigen. Antigen is generally detectable in nasopharyngeal and nasal secretions 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. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories are required to report all positive results to the appropriate public health authorities. Negative results should be treated as presumptive, and 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 patientâ??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. The Rapid Responseâ?¢ COVID-19 Antigen Rapid Test Device is for use at the Point of Care for professional use only.
PRODUCT INFORMATION:
Product: Rapid Respose
Sample: Nasal / Nasopharyngeal secretions
Format: Cassette
Quantity: 25 Tests/Kit per box
Time to result: 15 minutes
Storage Condition: 2-30 C/36-86 F
Test Principle: Immunochromatographic Assay
CONTENTS - Individually packed test devices
Extraction Buffer
Extraction tube
Nozzle with filter
Tube stand
Individually packed swabs
Package Insert
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
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.
Product Name:
Surplex(R)-COVID-19 IgM/IgG Rapid test
Product Description:
Surplex(R)-COVID-19 IgM/IgG Rapid test is a serology test intended for the qualitative detection of IgM and IgG antibodies of the novel coronavirus (the SARS-COV-2 virus) in human serum, plasma or whole blood. It is CE marked and approved in Brazil (ANVISA approved).
We are motivated to aggressively price our product and ready to send 20 tests (one box) to qualified buyers for evaluation, free of charge.
Price of product:
FOB USD $1.50 - $2.50 per test, volume dependent.
Product origin :
China.
Key Specifications/Special Features :
- Competitively priced and ready to ship in volume.
- Currently shipping in volume to Brazil.
- Highly accurate and specific - performance independently confirmed.
- Results ready in 15 minutes.
- Harmonization System (HS) Code: 382200.
- We provide a full support during regulatory application.
Minimum Order Size and Packaging details:
MOQ: Flexible.
Box of 20 or 50 test kits.
Storage: 2-30C.
Shelf Life: 10 months.
Combining practicality and comfort, our anti-slip bath mats feature a premium cotton top layer for softness and a non-slip latex or TPR (Thermoplastic Rubber) backing that firmly grips the floor surface. Designed to prevent bathroom accidents without compromising on aesthetics, these mats are ideal for homes, hotels, hospitals, care facilities, and wellness centres. Available in a variety of sizes, pile styles, and colors. Fully customizable for OEM and private label buyers.
Specifications
Material: Cotton Top + Latex / TPR Non-Slip Backing
GSM: 1400-1600 GSM (Top Layer)
Sizes: 45x75 cm, 50x80 cm, 60x90 cm
Colors: White, Custom
Safety Standard: Anti-Slip Tested
Clean Cell Phones are professionally tested, fully functional pre-owned mobile phones that have been inspected, data-wiped, cleaned, and graded for resale or export. These devices are ideal for wholesalers, retailers, refurbishers, and international buyers seeking reliable used smartphones at competitive prices.
If you are intrested Contact us:
Available inventory consists of 200 laptops from leading manufacturers, including Dell, HP, Lenovo, and Acer
Specifications:
Mixed brands such as Dell, HP, Lenovo, Apple, Acer, ASUS, or equivalent.
Various models with Intel Core i3/i5/i7 or AMD Ryzen processors.
Minimum 8 GB RAM (preferred).
SSD storage preferred (256 GB or above).
Fully tested and functional units.
Original chargers included where available.
Good cosmetic condition with no major defects.
We provide an ample range of Thermal Printer Paper for Fax Roll, Food Labels, Airline Tickets, Tags, Dispatch Labels, Bar code labels and many other carbonless applications. We have carved a niche as the most preeminent Thermal Paper Rolls Manufacturer and Thermal Paper Supplier in the Netherlands. Our Thermal Printer Paper exhibits countless features and has number of commercial uses. Manufactured from the premium quality base materials, our Thermal Printer Paper is the perfect blend of efficiency and performance.
APPLICATION AREAS
Sodium benzoate FCC/USP is used as a precursor, preservative and antioxidant in foodstuff, cosmetics, mouthwashes, water-based paint products. It is also employed as a flavoring agent, in food items, clinical reagents, diagnostic aid, and as a corrosion inhibitor in engine cooling structures.USP, or United States Pharmacopeia, grade chemicals comply with the standards of the United States Pharmacopeia .FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications.
Sodium Benzoate FCC/USP Grade Powder
WC Code: 19-007-01
Sales Specification
Appearance: White almost odourless, crystaline powder
Content(as dry product)%: 99.0
Loss on drying%: 1.5
Acidity or alkalinity: Passed test
Heavy metals%: 0.001
Chloride%: 0.02
Total Cl Content%: 0.03
Polycyclic acids: Passed test
As mg/kg: 2
Lead mg/kg: 2
Mercury mg/kg: 1
Readily oxidisable substances: Passed test
Sulfate%: 0.1
Transparency and color: Passed test
Phthalic acid: Passed test
Chroma: 20
Quality Standard
FCC 9 / USP38
Packing
50 lb bags , 24 bags per pallet
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