i. Rapid HIV Test Kits must have a minimum shelf life of one (1) year at the time of acceptance at the ordering agency. ii. The processing/established read time for the entire interpretation of the test is required to be within (1) minute to allow for the total patient encounter time of 10 minutes or fewer. iii. The test must be usable with finger stick, whole blood, or plasma. iv. Test accuracy must be 99% sensitivity and specificity or better. v. Test must be CLIA waived point-of-care. Provide the date of CLIA approval for the proposed product. vi. All test kits must be fully guaranteed to be free of defects first quality. All products found to be defective or expired within twenty (20) days of receipt must be replaced free of charge. Bidder is responsible for return shipment and replacement of product within five (5) business days vii. Testing Kits with support materials. 1. Single-use alcohol swab 2. Single-use lancet 3. Single-use pipette, capable of dispensing 50 ul viii. Materials required and available as an accessory to the kit. 1. One (1) HIV-1 reactive control 2. One (1) nonreactive control 3. One (1) product insert
