Product Description
Product details
| CAT No : | R0092C |
| Test Type | Rapid Test |
| Brand | CTK BioTech |
| Number of Reactions(Preps)/Kit | 10 |
| Result Time (Rapid Kits) | 15 min |
- Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
- Indicates protective immunity by detecting HAV IgG titers 70 mIU/mL
- High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
- Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
- Small sample volume (5 L) enables multiple testing on the same specimen without having to re-draw the patient.
- Initial patient care action can begin during the patients visit as test results are available in 15 minutes.
- Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
- One cassette device
- One desiccant
- 5 L capillary tubes
- Sample diluent (REF SB-R0092, 5 mL/bottle)
- Package insert (instruction for use)
Reliable and Rapid HAV IgM DetectionThis test delivers accurate detection of HAV IgM antibodies within just 15 minutes, helping healthcare professionals make timely decisions. Engineered with advanced immunochromatography, the kit is suitable for use with human serum, plasma, or whole blood. Its high sensitivity and specificity minimize the risk of false results, enhancing diagnostic confidence in busy clinical environments.
Easy-To-Use and Portable DesignPackaged as a lightweight, single-use device in an individually sealed pouch, the OnSite HAV IgM Rapid Test ensures convenience and portability. The test requires only manual handling and offers silent operation. Its visually marked cassette enables straightforward interpretation of results with clear positive or negative indications.
Comprehensive Kit for Professional SettingsEach box includes individually sealed cassettes, an instruction leaflet, and is traceable via its lot number. The test is specifically intended for professional use in clinical or laboratory settings and supports room temperature storage conditions. With an 18-24 month shelf life, it serves as a reliable solution for healthcare distributors, dealers, and suppliers across India.
FAQ's of OnSite HAV IgM Rapid Test:
Q: How is the OnSite HAV IgM Rapid Test used in a clinical setting?
A: To use the test, collect a sample of human serum, plasma, or whole blood. Add the specified amount to the test cassette, following the included instruction leaflet. Within 15 minutes, visually inspect for colored lines indicating a positive or negative result. The process is manual and does not require any external instrumentation.
Q: What sample types are compatible with this HAV IgM rapid test?
A: The test kit is validated for use with human serum, plasma, or whole blood, providing flexibility for different clinical scenarios and sample collection preferences.
Q: When can I expect to get the results after running the test?
A: Results are typically available within 15 minutes of adding the sample to the cassette, supporting real-time diagnostic decision-making in laboratory and clinical settings.
Q: Where should the OnSite HAV IgM Rapid Test be stored for optimal performance?
A: Store the test kits at temperatures between 2C and 30C, away from direct sunlight and frost. Proper storage extends the kit's shelf life and preserves test integrity.
Q: What is the benefit of using this HAV IgM rapid test kit in healthcare facilities?
A: The chief benefits include rapid and reliable detection (sensitivity >99%, specificity >98%), ease of use, portability, and room temperature storage. These features enable swift identification of HAV infection and facilitate better patient management.
Q: Is special training required to operate the HAV IgM Rapid Test?
A: The kit is intended for professional use in laboratories and clinics. Trained healthcare personnel can perform the test following the step-by-step instruction leaflet provided with each kit.
Q: What precautions should be taken during and after the test?
A: Always use a fresh, single-use test for each patient, and dispose of components following local biohazard waste guidelines. Avoid exposure to excessive heat, freezing, or moisture to maintain the test's accuracy and reliability.