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The Directigen™ EZ Flu A+B test is a rapid chromatographic immunoassay for the direct and qualitative detection of influenza A and B viral antigens from respiratory specimens of symptomatic patients.
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How to fill out BD Directigen™ EZ Flu A+B

01
Gather all necessary materials including the BD Directigen™ EZ Flu A+B kit.
02
Ensure that you are in a clean and sterile environment.
03
Collect the specimen swab from the patient’s nasal or throat area as indicated.
04
Insert the swab into the provided extraction buffer tube and swirl it to mix.
05
Remove the swab, ensuring that the liquid remains in the tube.
06
Follow the kit instructions to apply the sample to the testing device.
07
Wait for the specified amount of time as indicated in the kit instructions for results.
08
Read the results according to the interpretation guidelines provided in the kit.

Who needs BD Directigen™ EZ Flu A+B?

01
Patients exhibiting symptoms of influenza.
02
Healthcare providers needing to diagnose flu quickly.
03
Public health officials monitoring flu outbreaks.
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BD Directigen™ EZ Flu A+B is a rapid diagnostic test used to detect influenza virus type A and B in respiratory specimens. It provides results in a short period, aiding in the prompt diagnosis of flu infections.
Healthcare providers, laboratories, and clinics that use the BD Directigen™ EZ Flu A+B test are required to file results and comply with local regulations regarding reporting influenza cases.
To fill out BD Directigen™ EZ Flu A+B, follow the manufacturer's instructions, which include labeling the test with the patient’s information, properly collecting and processing the specimen, and recording results clearly and accurately.
The purpose of BD Directigen™ EZ Flu A+B is to quickly identify the presence of influenza virus in patients, helping clinicians make informed decisions on treatment and management of the illness.
Information that must be reported includes patient identification, date of the test, type of specimen collected, test results (positive/negative), and any applicable patient symptoms or demographics as required by local health authorities.
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