Product Description
| Brand | Abbott |
| Sample Type | Nasopharyngeal |
| Pack Size | 25T |
| CAT No | 19FK32 |
Bioline Influenza Ag A/B/A (H1N1) rapid test kit is a chromatographic immunoassay for the differential and qualitative detection of Influenza virus type A, type B and A (H1N1) antigens directly from nasal/throat/nasopharyngeal swab or nasal/nasopharyngeal aspirate specimens. This assay is intended for professional use and for in vitro diagnostic use only.
Fast, Reliable Influenza DetectionDesigned to provide rapid, qualitative results for influenza A, B, and A (H1N1), this test kit allows healthcare professionals to identify and differentiate flu infections within 15-20 minutes. The easy-to-use cassettes and visual indicators minimize interpretation errors and expedite clinical decision-making.
Simple Operation and Flexible Sample CollectionThe kit allows for versatile sample collection methods including nasopharyngeal swabs, throat swabs, nasal aspirates, or washes. Its user-friendly design requires no electricity and operates manually, making it suitable for a wide variety of clinical environments.
FAQ's of Abbott Bioline INFLUENZA Ag A/B/A (H1N1):
Q: How is the Abbott Bioline INFLUENZA Ag A/B/A (H1N1) test performed?
A: The test is performed manually by applying a collected respiratory specimen (such as a nasopharyngeal or throat swab, nasal aspirate, or wash) to the test cassette along with buffer solution. Results are interpreted visually within 15-20 minutes, following the instructions provided in the kit.
Q: What types of samples are compatible with this influenza test kit?
A: The kit is validated for nasopharyngeal swab, throat swab, nasal aspirate, or nasal wash specimens, allowing healthcare professionals flexibility in sample collection based on patient needs.
Q: When should the test be used during patient care?
A: For optimal diagnostic value, use the kit at the point of care when influenza infection is suspected, ideally during the early stages of symptoms, to guide timely clinical decisions and patient management.
Q: Where should the kit be stored to maintain effectiveness?
A: Store the test kit in a cool, dry place at temperatures between 1C and 30C. Avoid freezing and exposure to direct sunlight to maximize shelf life and maintain performance integrity.
Q: What is the benefit of using this rapid test over laboratory-based testing?
A: This rapid test provides results within 15-20 minutes, facilitating immediate diagnosis and management decisions without the need for laboratory equipment, thus saving critical time during influenza outbreaks.
Q: Who is authorized to use the Abbott Bioline INFLUENZA Ag A/B/A (H1N1) kit?
A: The kit is intended exclusively for use by healthcare professionals trained in specimen collection and test interpretation, ensuring proper and accurate application.
Q: What are the sensitivity and specificity rates for this test?
A: As per manufacturer data, sensitivity is approximately 90% for influenza A and 85% for influenza B, with specificity rates of about 97% for influenza A and 98% for influenza B. Actual accuracy may vary by batch; refer to the kit's instructions for use (IFU) for precise information.