INDICAID妥析新冠病毒快速抗原測試是香港政府指定快速測試品牌,並已取得美國FDA緊急使用授權及歐盟CE認證,檢測包括Delta及Omicron變種病毒。 INDICAID妥析新型冠狀病毒 (Covid-19) 快測讓您可隨時隨地自助測試新冠病毒。
INDICAID®COVID-19 Rapid Antigen Test is easy to use,
allowing you to self-test anytime and anywhere to detect the presence of the SARS‐CoV‐2 virus.
Suitable for
Close contact with COVID-19 patients / developed COVID-19 symptoms
Exposed to high occupational risk
Residents in high-risk areas
Families with elderly or children
Instruction
- Collect anterior nasal swab specimen
- Stir the swab into the buffer solution by twisting the swab back and forth 20 times
- Drop 3 drops of the buffer solution into the test device
- Read the results promptly in 20 minutes (results after 25 minutes should not be used)
Complete Instruction Guide: Download
- Wash your hands thoroughly with soap and water before collecting the specimen
- Swab at a well-ventilated area
- Maintain social distance of at least 2 meters while using the kit
- The test must be performed between 15-30°
- All components in this test kit are for one-time use only
- Store at 2-30°C. Do not freeze. Avoid direct sunlight
FAQs
Negative: A line appears in the region (C)
Positive: A line appears in regions (C) and (T)
Invalid Result: No line appears in the region (C)
Positive: A line appears in regions (C) and (T)
Invalid Result: No line appears in the region (C)
Positive Result: Please seek medical advice promptly, while your family members and close contacts should also get tested.
Negative Result: Regular testing (at least once every week) is recommended to protect yourself and your family members.
The accuracy of COVID-19 Rapid Antigen Test is measured under two metrics:
- Sensitivity: Measures the ability to correctly identify positive patient samples. If a test kit has a high sensitivity, it means that the kit has a high positive percentage agreement and a low false negative rate
- Specificity: Measures the ability to correctly identify negative patient samples. If a test kit has a high specificity, it means that the kit has a high negative percentage agreement and a low false positive rate
INDICAID® Rapid Antigen Test HK has passed extensive clinical validation. In HK Government’s Community Testing Scheme, INDICAID® has been used as part of the HK dual-track testing scheme along with COVID-19 PCR tests. As of January 2021, after the completion of 22994 clinical tests, it has been shown to reach accuracy comparable to PCR tests. This is the world's largest clinical study for a product of its kind.
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