Rapid Antigen Test Cassette

  • Price:

    Negotiable

  • minimum:

  • Total supply:

  • Delivery term:

    The date of payment from buyers deliver within days

  • seat:

    Beijing

  • Validity to:

    Long-term effective

  • Last update:

    2021-12-23 00:44

  • Browse the number:

    195

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Company Profile

Hihealth Medical Technology Co., Ltd

By certification [File Integrity]

Contact:huiruikang(Mr.)  

Email:

Telephone:

Phone:

Area:Beijing

Address:Beijing

Website:http://www.hihealthcn.com/ http://huiruikang.miaoyincn.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/