1. Selelekela
This manual provides detailed instructions for the proper use of the INDICAID COVID-19 Antigen Rapid Test. This test is an in vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigen from direct anterior nasal swab specimens. It is intended for self-administration by individuals aged 15 years or older, or by an adult for children aged 2-14 years.
The INDICAID COVID-19 Antigen Rapid Test is authorized for emergency use by the FDA for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. The emergency use of this product is authorized only for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb3(b)(1), unless the declaration is terminated, or authorization is revoked sooner.
Image 1.1: INDICAID COVID-19 Antigen Rapid Test Kit Packaging.
2. Likarolo tsa Sehlahisoa
Each INDICAID COVID-19 Antigen Rapid Test kit contains the following components:
Image 2.1: Contents of the INDICAID COVID-19 Antigen Rapid Test Kit.
- Sesebediswa sa Teko: Individually sealed pouch containing a test cassette.
- Buffer Solution Vial: Pre-filled tube with extraction buffer.
- Nasal Swab: Sterile swab for specimen collection.
- Litaelo tsa Tšebeliso: Bukana ena.
Ensure all components are present and undamaged before proceeding with the test.
3. Seta le Tokisetso
Before starting the test, please follow these preparation steps:
- Read the entire instruction manual carefully before performing the test.
- Wash your hands thoroughly with soap and water for at least 20 seconds, then dry them completely.
- Open the kit box and place all components on a clean, flat surface.
- Check the expiration date on the kit box and individual component packaging. Do not use expired tests.
- Ensure the test device pouch is intact and open it just before use.
4. Litaelo tsa Ts'ebetso
Follow these steps precisely to perform the INDICAID COVID-19 Antigen Rapid Test:
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Step 1: Collect Nasal Swab Sample
Carefully open the sterile nasal swab package. Insert the entire soft tip of the swab into one nostril about 1/2 to 3/4 inch (1 to 1.5 cm) until resistance is met. Rotate the swab 5 times against the nasal wall. Using the same swab, repeat the process in the other nostril. Withdraw the swab from the nostril.
Image 4.1: Proper nasal swab collection technique.
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Mohato oa 2: Lokisetsa Sample
Unscrew the cap of the buffer solution vial. Insert the swab tip into the buffer solution vial. Swirl the swab vigorously in the solution 10 times, pressing the tip against the bottom and sides of the vial to ensure the sample is thoroughly mixed with the buffer. Remove the swab while squeezing the sides of the vial to extract as much liquid as possible from the swab tip. Dispose of the swab in a biohazard bag or household waste.
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Step 3: Apply Sample to Test Device
Place the dropper cap firmly onto the buffer solution vial. Invert the vial and add three (3) drops of the solution into the sample well (S) of the test device. Do not touch the test device with the dropper tip.
Image 4.2: Applying sample to the test device (left side of image) and result interpretations (right side).
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Mohato oa 4: Emela Liphetho
Set a timer for 20 minutes. Read the results at exactly 20 minutes. Do not read the results before 20 minutes or after 25 minutes, as this may lead to inaccurate readings.
5. Ho Toloka Liphetho
Refer to Image 4.2 for visual examples of result interpretations. The test device has two lines: a Control Line (C) and a Test Line (T).
- Sephetho se setle: Two colored lines appear. One colored line appears at the Control Line (C) region and another colored line appears at the Test Line (T) region. Any faint line at the T region should be considered positive. A positive result indicates the presence of SARS-CoV-2 antigens.
- Sephetho se Fosahetseng: One colored line appears at the Control Line (C) region. No colored line appears at the Test Line (T) region. A negative result indicates that SARS-CoV-2 antigens were not detected.
- Sephetho se sa nepahalang: No colored line appears at the Control Line (C) region, or only a colored line appears at the Test Line (T) region. An invalid result indicates that the test did not work correctly. In this case, discard the test and repeat with a new test kit. If the issue persists, contact customer support.
A positive result does not rule out co-infections with other pathogens. A negative result does not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions.
6. Tlhokomelo le Poloko
Proper handling and storage ensure the reliability of the test kit.
- Polokelo: Store the test kit at room temperature, between 2°C to 30°C (36°F to 86°F), away from direct sunlight and moisture.
- Ho felloa ke nako: Do not use the test kit beyond the expiration date printed on the packaging. The FDA has granted a shelf-life extension for this product, increasing its shelf life from 6 months to 15 months. Always check the updated expiration date if available.
- Ho lahla: After use, place all test components in a sealed plastic bag and dispose of them with household waste according to local regulations.
Setšoantšo sa 6.1: Example of Lot Number and Expiration Date on product packaging.
7. Ho rarolla mathata
Haeba o kopana le mathata nakong ea teko, sheba mathata le litharollo tse latelang tse tloaelehileng:
| Bothata | Lebaka le ka khonehang | Tharollo |
|---|---|---|
| No Control Line (C) appears. | Test device malfunction or insufficient sampbophahamo ba modumo. | The result is invalid. Repeat the test with a new kit. Ensure 3 drops of solution are added to the samphantle. |
| Test Line (T) is very faint. | Low concentration of antigen or early stage ea tšoaetso. | Any visible line at the T region, no matter how faint, should be considered a positive result. Consult a healthcare professional. |
| Results read after 25 minutes. | Delayed reading can lead to inaccurate results (false positives or negatives). | The result may be unreliable. Repeat the test with a new kit, ensuring results are read at exactly 20 minutes. |
Bakeng sa thuso e eketsehileng, ka kopo ikopanye le ts'ehetso ea bareki.
8. Litlhaloso
- Lebitso la Sehlahiswa: INDICAID COVID-19 Antigen Rapid Test
- Mohlala: Teko e potlakileng ea COVID-19 Antigen
- Moetsi: Indicaid
- Boholo ba Sephutheloana: 7.99 x 2.6 x 1.06 lisenthimithara
- Boima ba 'mele: 1.76 lik'hilograma
- Letsatsi la Pele la ho Fumana: La 18 Phupu 2022
- Shelf Life: Up to 15 months (check specific expiration date on packaging)
- Nako ea Teko: metsotso e 20
9. Tiisetso le Tšehetso
For information regarding product warranty, please refer to the official INDICAID website or contact their customer support directly. If you have questions or require assistance with your INDICAID COVID-19 Antigen Rapid Test, please reach out to the manufacturer's customer service.
U ka fumana boitsebiso bo eketsehileng le lisebelisoa tsa tšehetso ho INDICAID Brand Store.