Products
A company specializing in the development, production and sales of in vitro diagnostic products.
Product classification
Contact Us
Phone/WeChat:
E-mail:
info@immuno-test.com
Address:
Building 1, 578 No.20 Street, Qiantang District, Hangzhou City, Zhejiang Province
Influenza A Antigen Rapid Test
Phone:0571-85368996 | Email:info@immuno-test.com
Abbr.:
Specification:
Specimen:
Assay Time:
Model No.:
HFLU015GA
Model No.: HFLU015GA
Assay Time: 10-15 minutes
Specimen: Nasopharyngeal swab, or oropharyngeal swab specimen
Influenza A Antigen Rapid Test
Graphic Details
INTENDED USE
The Influenza A Antigen Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of Influenza A antigen in human nasopharyngeal swab, or oropharyngeal swab specimen in individuals who are suspected of respiratory viral infection consistent with flu symptoms.
[Product Name] | Influenza A Antigen Rapid Test |
[Product No.] | HFLU015GA |
[Assay Time] | 10-15 minutes |
[Specimen] |
Nasopharyngeal swab, or oropharyngeal swab specimen. |
[Storage Temperature] | 2-30℃, DO NOT FREEZE |
[Usage] | The Influenza A Antigen Rapid Test is designed as a simple tool in detection of influenza A for regular clinical diagnosis. |
[Packing] | 20 tests/box |
PRINCIPLE
The Influenza A Antigen Rapid Test is consist with one test strips which could be observed in the window of the rapid test device. The strip is based on sandwich method immunochromatographic assay.
STORAGE AND STABILITY
- The kit can be stored at room temperature or refrigerated (2-30°C). The Test Strip is stable through the expiration date printed on the sealed pouch. The Test device must remain in the sealed pouch until use.
- DO NOT FREEZE.
- Do not use beyond the expiration date. The stability of the kit under these storage conditions is 24 months.
- Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation.
MATERIALS PROVIDED
1. Individually packed test device
2. Assay buffer tubes (0.5ml each) with tips
3. Disposable Sampling Swabs
4. Workstation
5. Package insert
SPECIMEN COLLECTION AND PREPARATION
Nasopharyngeal Swab: Insert the sterile swab into the deep nasal cavity until the nasopharynx. Gently rub and
rotate the swab against wall of turbinate for several times.
TEST PROCEDURE
Allow the rapid test, specimen, buffer, and/or controls to equilibrate toroom temperature (10-30°C) prior to testing.
1. Prepare the specimen
2. Remove the rapid test device from the sealed pouch and use it as soon as possible.
3. Place the test device on a clean and horizontal surface. Reverse the assay buffer tube, extrude 3 drops (about 70μL) of the prepared specimen into the specimen well (S) of the test device and start the timer.
4. Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret the result after 15 minutes.
INTERPRETATION OF RESULTS
POSITIVE: Two colored bands appear on the membrane. One band appears in the control region (C) and another band appears in the test region (T).
NEGATIVE: Only one colored band appears in the control region (C). No apparent colored band appears in the test region (T).
INVALID: Control band fails to appear.
Previous Page
Previous Page
Related Products
Online message