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PDX 010603800WHO PQ Public Report March 2019; version 3.WHO Prequalification of In Vitro Diagnostics
PUBLIC REPORT
Product: DSEIAHIVAGABSCREEN
WHO reference number: PDX 010603800
DSEIAHIVAGABSCREEN
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How to fill out product ds-eia-hiv-agab-screen
01
Start by reading the instructions and familiarizing yourself with the product ds-eia-hiv-agab-screen.
02
Make sure you have all the necessary materials and equipment, such as the test kit, specimen collection devices, and reagents.
03
Wash your hands thoroughly with soap and water before starting the process.
04
Open the test kit and remove all the components. Ensure that they are in good condition and have not expired.
05
Use the specimen collection device provided to collect a sample, following the instructions on how to properly collect the specimen.
06
Place the collected specimen into the appropriate container or well, as indicated in the instructions.
07
Add the required reagents to the specimen, according to the specified volumes and order.
08
Mix the contents gently by swirling or inverting the container a few times.
09
Incubate the mixture at the specified temperature and time, following the instructions.
10
After the incubation period, read the results based on the provided guidelines. Interpret the results accurately and record them if necessary.
11
Dispose of all used materials and the test kit, following the proper waste disposal guidelines.
12
Clean up your work area and wash your hands thoroughly with soap and water.
13
Refer to the provided instructions for any additional steps or precautions that may be required.
Who needs product ds-eia-hiv-agab-screen?
01
Product ds-eia-hiv-agab-screen is needed by healthcare professionals, laboratories, or individuals who want to screen for HIV antibodies and antigen.
02
It is commonly used in healthcare settings, blood banks, diagnostic laboratories, and public health clinics.
03
Anyone who suspects exposure to HIV or wants to get tested for HIV can benefit from using this product.
04
It is important to consult healthcare professionals or follow local regulations and guidelines for HIV screening and testing.
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What is product ds-eia-hiv-agab-screen?
Product ds-eia-hiv-agab-screen is a diagnostic test kit for detecting HIV antibodies and antigens.
Who is required to file product ds-eia-hiv-agab-screen?
Medical professionals and healthcare facilities conducting HIV screening are required to file product ds-eia-hiv-agab-screen.
How to fill out product ds-eia-hiv-agab-screen?
Product ds-eia-hiv-agab-screen should be filled out by following the instructions provided in the kit or as per the guidelines set by the regulatory authorities.
What is the purpose of product ds-eia-hiv-agab-screen?
The purpose of product ds-eia-hiv-agab-screen is to screen individuals for HIV infection.
What information must be reported on product ds-eia-hiv-agab-screen?
Product ds-eia-hiv-agab-screen must include patient information, test results, and any additional details required for reporting purposes.
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