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SARS-CoV-2 & Influenza A/B Rapid Antigen Test Cassette
Rapid detection and differentiation between SARS-CoV-2, Influenza A and B.
The SARS-CoV-2 & Flu A/B Rapid Antigen Test helps healthcare professionals at the point of care to quickly detect and differentiate infections with any of the three respiratory viruses and aid in pursuing appropriate courses of action, including patient management decisions. Also, it enables scaling up test capacities during flu season to meet the need for extensive testing during peak periods.
Rapid answers, combined
Fast detection and differentiation between SARS-CoV-2, Influenza A and Influenza B virus with a truly integrated test requiring a single sample to optimize patient care.
Date sheet
Product name:
SARS-CoV-2 & Influenza A/B Rapid Antigen Test Cassette
Format:
Card
Specimen:
Swab
Sensitivity:
99.9%
Accuracy:
>99.99%
Specificity:
99.99%
Packing
25pcs/box; 5pcs/box; 1pcs/box
shelf life
2years
Certificate:
CE , FSC
Directions for Use
Allow the test, specimen, extraction buffer to equilibrate to room temperature (15-30°C) prior to testing.
1. Remove the test device from the sealed foil pouch and use it as soon as possible.
Place the test device on a clean and level surface. Best results will be obtained if the assay is performed immediately after opening the foil pouch.
2. Take out one extraction tube with buffer, pull off the sealed aluminum foil on the extraction tube and place extraction tube in the tube stand or in the hole in the box.
3. Place the sterilized swab specimen in the sample extraction buffer. Rotate the swab for approximately 10 seconds while pressing the head against the inside of the tube to release the antigen in the swab.
4. Remove the sterilized swab while squeezing the sterilized swab head against the inside of Buffer as you remove it to expel as much liquid as possible from the swab. Discard the sterilized swab in accordance with your biohazard waste disposal protocol.
5. Screw on and tighten the Nozzle with Filter onto the specimen collection tube, then shake the specimen collection tube vigorously to mix the specimen and the sample extraction buffer. See illustration 4.
6. Add 3 drops of the solution (approx.80ul) to each sample well and then start the timer. Read the result at 15~20 minutes. Don’t interpret the result after 20 minutes.
7. Please dispose the test materials which put in a closed plastic bag with the household trash. If there are local regulations, please follow them. 8. Wash hands thoroughly after test completion
POSITIVE SARS-Cov-2: Two red lines appear. One red line appears in the control region(C), and one red line in the test region(T).
POSITIVE Influenza A: Two distinct colored lines appear. One colored line should be in the control region (C) and another colored line should be in the Influenza A region (A). A positive result in the Influenza A region indicates that Influenza A antigen was detected in the sample.
POSITIVE Influenza B: Two distinct colored lines appear. One colored line should be in the control region (C) and another colored line should be in the Influenza B region (B). A positive result in the Influenza B region indicates that Influenza B antigen was detected in the sample.
POSITIVE Influenza A and Influenza B: Three distinct colored lines appear. One colored line should be in the control region (C) and two colored line should be in the Influenza A region (A) and Influenza B region (B). A positive result in the Influenza A region and Influenza B region indicates that Influenza A antigen and Influenza B antigen were detected in the sample.
*NOTE: The shade of color may vary, but it should be considered positive whenever there is even a faint line.
If the test result is positive, please keep social distant to not spread infection, to follow local guidelines about social distance.
NEGATIVE: Only one red line appears in the control region(C), and no line in the test region(T/A/B). If you have symptoms like fever, cough and/or shortness of breath. Please retest in 1-3 days. You must continue following the applicable hygiene and distancing rules even with a negative result.
INVALID: No red line appears in the control region(C). The test is invalid even if there is a line on test region(T/A/B). Insufficient sample volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the test procedure and repeat the test using a new test device.
Certifications
2022 MEDICA in Germany
Date: from November 14th to November 17th
Add.: Messe Düsseldorf
Hall: 01
Out booth No: 1H39
FAQ
Q: What is your payment terms?
A: Payment terms: 100% TT before shipment
Q: Can you send samples?
A: Yes,SAMPLES can be sent for your evaluation.customer pay the freight charge
Q: Do you give any discount? A: I'll surely try my best to help you get those by the best price and good service at the same time. We promise the best price upon same quality, and best quality upon same price. Q: How to order? A: Please tell us the model and quantity and package requests. B. Proforma Invoice confirmed, the order will be arranged upon receipt of your payment. C. Confirm and ship the goods. D. We will help to track your goods until you receive them safely.
Company Details
Bronze Gleitlager
,
Bronze Sleeve Bushings
and
Graphite Plugged Bushings
from Quality China Factory
Business Type:
Manufacturer,Exporter,Trading Company
Year Established:
2014
Employee Number:
>1000
Ecer Certification：
Verified Supplier
Innovation Biotech (Beijing) Co.,Ltd is a biotechnology company specializing in research, development and manufacturing of advanced medical in-vitro diagnostic (IVD) rapid test kits, medical and laboratory disposal products. We provide one step medical diagnostic rapid test kit based on our INVBIO b... Innovation Biotech (Beijing) Co.,Ltd is a biotechnology company specializing in research, development and manufacturing of advanced medical in-vitro diagnostic (IVD) rapid test kits, medical and laboratory disposal products. We provide one step medical diagnostic rapid test kit based on our INVBIO b...
