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15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit

Basic Information
Place of Origin: China
Brand Name: Dewei
Certification: CE White List
Model Number: DWR-800AG
Minimum Order Quantity: 10000pcs
Price: $1.50-2.0/pcs
Packaging Details: 25tests/box
Delivery Time: 5-20 days
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 100000pcs/day
Detail Information
Sample Collection: Oral Or Nasal Swab Package: 25pcs/box
Use: Fast Check Of Coronavirus Reading Time: 15 Mins
Method: Colloidal Gold Assay Qualitative: Qualitative Determination Of Covid-19
High Light:

2019-NCoV Rapid Test Kit

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Covid POCT Rapid Test Kit

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15mins Reading Antigen Test Kit


Product Description

15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit

Colloidal Gold Assay

² Fast: 15 Minutes

² Easy: One Step

² Convenient: Throat/Nasal swab sample

² Cheap: Lower cost with high efficiency

 

INTEND USE  

The rapid test kit is used for qualitative determination of novel coronavirus (SARS-CcV-2) antigen in human nasal swab samples in vitro.. This kit is offered to clinical laboratories and healthcare workers for point-of-care testing, and not for at home testing, in compliance with Section IV.D. of the FDA’s Policy for COVID-19 Diagnostic Test.

 

MAIN COMPONENTS  

• Test Cassette.

• Extraction Tube.

• Extraction Reagent.

• Nasal/Oral Swab.

• Working Holder.

 

STORAGE & STABILITY

•  Store at 39 ~ 86 º F (4 ~ 30 º C) in the sealed pouch up to the expiration date.

•  Keep away from direct sunlight, moisture and heat.

•  DO NOT FREEZE.

 

HOW TO PERFORM THE TEST?

1. Remove a Test Device from the foil pouch by tearing at the notch and place it on a level surface.

2. Holding Extraction Reagent bottle vertically, add 10 drops (400μL) to the Extraction tube.

3. Insert the nasopharyngeal (and oropharyngeal) swab sample(s) into the extraction solution, then, mix the swab 10 times.

4. Remove the swabs while pressing against the solution tube in order to extract most of the specimen

5. Place the dropper cap and drop 3 drops (60~70μl) into the sample well.

6. Read the result in 10-15 minutes. Do not read results after more than 20 minutes.

 

15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit 0

 

REANDING RESULTS

Negative :

Only one color line appears on the control region.

Positive :

Two bands are appeared in the test line (T) and control line (C).

Invalid:

No visible line at all, or there is a visible line only in the test region and not in the control region. Repeat with a new test kit. 

15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit 1

 

Something you need to learn about:

1) What is the difference between an antigen test and a molecular test?

An antigen test detects specific proteins on the surface of the virus. These tests are quicker and less expensive, but have a higher chance of missing an active infection, according to the FDA.

A molecular (PCR or polymerase chain reaction) test detects the virus’s genetic material. These tests require a more complex technology to get results, and it usually takes a day or two to get those results (depending on lab capacity, results may take up to a week).

If an antigen test shows a negative result and you have reason to believe you may have the virus (because of symptoms or exposure), your doctor may order a molecular test to confirm the results.

 

2) Which tests are more accurate?

No test is 100% accurate, but the molecular tests are considered to be more accurate than the antigen tests, according to available research.
According to the FDA, an antigen test cannot “definitively rule out active coronavirus infection,” but positive results are “highly accurate” (negative results may require a confirmation test).
Harvard Medical School wrote in August that the reported rate of false negatives with molecular testing is as low as 2% and as high as 37%. A molecular test using a deep nasal swab will have fewer false negative results than samples from throat swabs or saliva, they say.
For antigen testing, Harvard noted that the reported rate of false negative results can be as high as 50%, but that the FDA has granted emergency use authorization for a more accurate antigen test.
In general, some of the issues that may affect the accuracy of a test include ineffective swabbing, contamination or mishandling of the sample, or problems with the testing chemicals, according to the FDA.

 

3) If antigen tests are less accurate, why would we use them?
Experts say the value in the rapid antigen tests is in the frequency of the testing rather than the accuracy, with repeated testing recommended. According to Science, getting a false negative in an antigen test two or three times in a row is rare. This strategy lines up with the NPR report mentioned above, which would employ daily testing of those in high-risk areas.

 

4) Who must be tested for COVID-19?
As per the Minister’s Directive: COVID-19: Long-Term Care Home Surveillance Testing and Access to Homes (Minister’s Directive) effective January 8, 2021, all staff, student placement and volunteers working in long-term care homes must be tested regularly in accordance with the Minister’s Directive, unless the exception for individuals who have previously had laboratory confirmed COVID-19 applies. The testing requirements in the Minister’s Directive include all individuals working in long-term care homes who are: • Staff as defined in the Long-Term Care Homes Act, 2007 • Volunteers as defined in the Long-Term Care Homes Act, 2007 • Student placement, meaning any person working in the long-term care home as part of a clinical placement requirement of an educational program of a college or university, and who does not meet the definition of “staff” or “volunteer” under the Long-Term Care Homes Act, 2007. The Minister’s Directive also includes additional testing and documentation requirements for general visitors, caregivers and support workers.

 

5) When should you perform Dewei COVID-19 Ag Rapid Test?
The COVID-19 Ag Rapid test should NOT be used for diagnosis of COVID-19 infection. Any individual who is symptomatic or a contact of a confirmed case should be directed to their healthcare provider, an assessment centre, or participating licensed community lab to seek PCR testing.

 

6) Do long-term care homes have to conduct the rapid antigen tests themselves?
The ministry is exploring developing a Vendor of Record to connect LTC homes wishing to contract with providers to conduct surveillance screening clinics on their behalf in the LTC home. The ministry would look to developing and providing the necessary templates and service agreements to support licensees in making decisions regarding entering into contracts with providers and the terms and conditions on which services are provided. The Vendor of Record would be optional and would not prevent homes from contracting with a qualified vendor that is not on this roster.

 

 
PACKAGE
15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit 215mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit 3
15mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit 415mins Reading One Step Covid POCT Covid-19 2019-NCoV Antigen Rapid Test Kit 5

Contact Details
Sherry

Phone Number : +8613316305166

WhatsApp : +008615267039708