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Kissh
KISSH - 新冠病毒抗原快速測試棒 (唾液版) (1盒) [COVID-19 快速測試 自我檢測 Omicron & Delta適用]
15-minute rapid test for Omicron & Delta variant virus, this product is used for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigen in saliva samples.
Internationally recognized by the United Kingdom, Germany, Thailand, etc.
Recognized by German PEI test results, specificity and sensitivity >99%
Thailand FDA certification, the test specificity for the new coronavirus is 100% and the sensitivity is as high as 98%
Obtain excellent performance data with 100% sensitivity and specificity in a Malaysian laboratory officially accredited by the World Health Organization (WHO)
Passed the British MHRA (Medicines & Healthcare products Regulatory Agency) 3A certification
Approved by the Indonesian Ministry of Health
Obtained EU CE and ISO 13485 certification
Obtained listing whitelists in multiple countries, including Germany, France, Thailand FDA, Indonesia, Malaysia, and European general lists
Stable and superior performance, qualitative detection is easy to interpret
....................................................................
Storage method: The product should be stored in a cool place at 2~30°C. The validity period is 18 months. It is forbidden to store below 2°C and avoid using expired products.
Manufacture Date (MFD) and Expiry Date (EXP): Marked on the label.
Precautions:
1. For in vitro diagnosis.
2. This product is only authorized for the detection of SARS-CoV-2 nucleocapsid protein, not for any other viruses or pathogens.
3. Proper sample collection and handling are critical to correct results.
4. Keep the Test Card sealed in the foil pouch until just before use. Do not use if pouch is damaged or opened.
6. Do not use expired kits.
7. Do not mix Test Cards and Sample Extraction Buffer from different kit lots.
8. All kit components are disposable. Do not use with multiple specimens. Do not reuse used Test Cards.
9. Do not use damaged packaging components and extraction tubes that have been damaged after mixing the solution with a swab.
10. If you have any questions, please consult a professional doctor. Users should not make any medical-related decisions on their own.
Internationally recognized by the United Kingdom, Germany, Thailand, etc.
Recognized by German PEI test results, specificity and sensitivity >99%
Thailand FDA certification, the test specificity for the new coronavirus is 100% and the sensitivity is as high as 98%
Obtain excellent performance data with 100% sensitivity and specificity in a Malaysian laboratory officially accredited by the World Health Organization (WHO)
Passed the British MHRA (Medicines & Healthcare products Regulatory Agency) 3A certification
Approved by the Indonesian Ministry of Health
Obtained EU CE and ISO 13485 certification
Obtained listing whitelists in multiple countries, including Germany, France, Thailand FDA, Indonesia, Malaysia, and European general lists
Stable and superior performance, qualitative detection is easy to interpret
....................................................................
Storage method: The product should be stored in a cool place at 2~30°C. The validity period is 18 months. It is forbidden to store below 2°C and avoid using expired products.
Manufacture Date (MFD) and Expiry Date (EXP): Marked on the label.
Precautions:
1. For in vitro diagnosis.
2. This product is only authorized for the detection of SARS-CoV-2 nucleocapsid protein, not for any other viruses or pathogens.
3. Proper sample collection and handling are critical to correct results.
4. Keep the Test Card sealed in the foil pouch until just before use. Do not use if pouch is damaged or opened.
6. Do not use expired kits.
7. Do not mix Test Cards and Sample Extraction Buffer from different kit lots.
8. All kit components are disposable. Do not use with multiple specimens. Do not reuse used Test Cards.
9. Do not use damaged packaging components and extraction tubes that have been damaged after mixing the solution with a swab.
10. If you have any questions, please consult a professional doctor. Users should not make any medical-related decisions on their own.
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