Product Description
- BrandSD Biosensor
- Sample TypeNasopharyngeal
- Pack Size25T
- CAT No09COV102D
STANDARD Q COVID/Flu Ag Combo Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 and Influenza A and Influenza B present in human nasopharyngeal specimens.
Quick and Efficient DiagnosisObtain accurate results in as little as 15-30 minutes with the STANDARD Q COVID/Flu Ag Combo kit. Its rapid turnaround helps healthcare professionals make timely decisions regarding patient management and infection control, especially during peak respiratory infection seasons.
Designed for Healthcare ProfessionalsThe test kit is tailored for use by trained personnel, ensuring reliable results through standardized procedures. Easy-to-follow instructions, along with the included swabs and buffers, streamline the testing process in various clinical environments.
High Performance and Reliable ResultsThis test offers high sensitivity and specificity for both COVID-19 and Influenza A/B, reducing the risk of false results. The qualitative, colored line indicator system provides clear, visual interpretation without the need for special equipment.
FAQ's of SD Biosensor STANDARD Q COVID/Flu Ag Combo:
Q: How is the STANDARD Q COVID/Flu Ag Combo test performed?
A: The test is performed by collecting a nasopharyngeal swab specimen, mixing it with the provided extraction buffer, and applying the mixture to the test device. The results are then visually interpreted using colored lines within 15-30 minutes.
Q: What benefits does this combo diagnostic kit provide?
A: This kit enables simultaneous detection of both COVID-19 and Influenza A/B viruses, allowing rapid differentiation and informed treatment decisions. Its high accuracy, fast results, and portability make it valuable in clinics, hospitals, and field settings.
Q: When should the STANDARD Q COVID/Flu Ag Combo be used?
A: The kit should be used when rapid detection of respiratory infections is required, particularly in patients presenting with symptoms common to both COVID-19 and influenza. It is suitable during outbreaks or when differential diagnosis is critical.
Q: Where can this test be administered?
A: The test is intended for use in medical settings like clinics, hospitals, and laboratories by healthcare professionals or trained personnel, ensuring safe and proper specimen collection and result interpretation.
Q: What is the recommended sample type for this test?
A: A nasopharyngeal swab specimen is required for this test, as it optimally collects respiratory viral antigens necessary for accurate detection.
Q: How should the test kits be stored?
A: Store the test kits at temperatures between 2C and 30C, away from direct sunlight. Proper storage helps maintain the integrity and accuracy of the tests throughout their 18-month shelf life.