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HIV 1/2 STAT-PAK® Assay
HIV 1/2 STAT-PAK® Assay
This document provides details about an FDA-approved rapid point-of-care assay for detecting HIV-1 and HIV-2 antibodies in various blood samples. The assay is known for its superior performance, innovative design, and ease of use.
Specifications
- Performance: The test exceeds WHO performance thresholds with a sensitivity of 99.7% and specificity of 99.9%.
- Sample Volume: Requires only 5 µl of sample.
- Method: Utilizes lateral flow technology.
- Shelf Life: 24 months from the date of manufacture.
- Storage Conditions: 8 - 30°C (46-86°F).
- Time to Results: 15 minutes.
Procedure
- Transfer the sample to the Sample Well (S).
- Add 3 drops of running buffer to the Sample Well (S).
- Wait 15 minutes and read the results as either non-reactive or reactive.
Product Information
- Catalog Number: HIV 1/2 STAT-PAK® Assay - 60-9505-1.
- Reimbursement Codes: 86703, 86703QW, G0435 (for Medicare).
Additional Information
For more details, visit the Chembio website, call their support line, or email them directly.
Catalog excerpts
Performance Matters An FDA approved, rapid point-of-care assay for the detection of HIV-1 and HIV-2 antibodies in fingerstick or venous whole blood, serum or plasma. Superior Performance • The only HIV test that exceeds WHO performance thresholds1 • Sensitivity: 99.7%; Specificity: 99.9%2 Innovative Design • Small sample volume: 5 pi • Built-in procedural control Easy to Use • Test in 3 easy steps: Prepare, Run, Read • Requires minimal training 1 Kosack CS et al. Journal of the International AIDS Society 2017, 20:21345 2 Refer to product insert for details
Open the catalog to page 1
Product Information Information Type * From date of manufacture Reimbursement Codes: 86703 or 86703QW G0435 (for Medicare) For More Information Visit: www.chembio.com Call: 1.844.CHEMBIO Email: [email protected] © Copyright 2018, Chembio Diagnostic Systems, Inc. The Chembio logo and STAT-PAK are trademarks of Chembio Diagnostic Systems, Inc. ® Indicates a Chembio trademark registered in the USA. MS-12-009 Rev 7
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