Rapid Antigen Test Cassette
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Price:
Negotiable
- minimum:
- Total supply:
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Delivery term:
The date of payment from buyers deliver within days
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seat:
Shandong
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Validity to:
Long-term effective
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Last update:
2021-10-08 01:36
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Browse the number:
242
Company Profile
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By certification [File Integrity]
Contact:huiruikang(Mr.)
Email:
Telephone:
Phone:
Area:Shandong
Address:Shandong
Website:http://www.rapidtestcn.com/ http://huiruikang.xmlqpx.com/
Product Details
Product Details
Product Name: Rapid Antigen Test Cassette
Sample type: Nasopharyngeal swab; oropharyngeal swab
Storage condition: Store as packaged in the sealed pouch at the temperature (4-30℃ or 40-86℉).
Shelf Life: 24 months from the date of manufacture
Certificate: FDA, CE
Packing Specification: 25 test/ box.
Kit Contents |
20 Test Cassettes |
1 Package Insert |
20 Extraction Tubes |
20 Dropper Tips |
|
20 Sterilized Swabs |
2 Extraction Reagents |
The Rapid Antigen Test Cassette is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen in direct nasopharyngeal (NP) swab from individuals who are suspected of by their healthcare provider. It is intended to aid in the rapid diagnosis of infections.
Specimen collection
Utilize the nasopharyngeal swab provided in the unit.
1. Cautiously embed the swab into the nostril of the patient, arriving at the outside of the back nasopharynx. that presents the most secretion under visual inspection.
2. Swab over the outside of the back nasopharynx. Turn the swab a few times.
3. Pull out the swab from the nasal depression.
Test procedure & interpretation of results
1.POSITIVE:
The presence of two lines as control line (C) and test line (T) inside the outcome window demonstrates a positive outcome.
2.NEGATIVE:
The presence of just control line(C) inside the outcome window shows a negative outcome.
3.INVALID:
In the event that the control line (C) isn't obvious inside the outcome window in the wake of playing out the test, the outcome is viewed as invalid. A few reasons for invalid outcomes are a result of not after the bearings effectively or the test may have disintegrated past the termination date. It is suggested that the example be re-tried utilizing another test.
Clinical Evaluation
Positive Percent Agreement (PPA): 95.7%
Negative Percent Agreement (NPA): 99.6%
Overall Percent Agreement (OPA): 98.9%
Features
Qualitative, visually read results in 15 minutes
No instrument required
Procedural internal control included
Company Advantage
Excellent Product Quality
Passed Various Professional Certifications such as CE/TUV/FDA/EUV
Comprehensive Enterprise
10 Years of Experience
Factory Direct Supply
Overseas Warehouse, Fast Shipment
After-Sales Service
Money-Back Guarantee
Prompt Customer Service Guarantee
http://www.hihealthcn.com/