Rapid antibody tests serve as screening tools and have limitations related to the window period and antibody kinetics. Negative results early in infection may not rule out infection. Positive results should be confirmed with recommended laboratory assays following local algorithms. Always perform testing using proper biosafety precautions and dispose of clinical waste according to local regulations.
Abbott Determine HIV-1/2 Rapid Card — Product Description
The Abbott Determine HIV-1/2 Rapid Card is a high-performance lateral-flow immunoassay designed for the rapid detection of antibodies to HIV-1 and HIV-2 in human serum, plasma, or whole blood. It delivers convenient, reliable results in approximately 15 minutes, making it well suited for both point-of-care screening and clinical laboratory workflows.
Built for ease of use in diverse settings—including hospitals, diagnostic laboratories, community health centers, and field screening programs—the Determine Rapid Card supports quick decision-making by healthcare professionals. Its long shelf life and compact format make it a cost-effective screening option in surveillance and outreach contexts.
Key Features :
- Rapid antibody detection for HIV-1 and HIV-2 with results in ~15 minutes.
- Suitable for serum, plasma, and whole blood specimens (confirm specimen type per IFU).
- Compact lateral-flow card format — ideal for point-of-care testing and field use.
- Long shelf life and room-temperature storage (check kit label for exact conditions and expiry).
- Simple visual readout — easy to interpret when used according to instructions.
- Cost-effective option for screening, surveillance, and triage where rapid turnaround is needed.
Important: This rapid antibody test is intended for screening. Results should be interpreted in the context of clinical findings and local testing algorithms. Reactive (positive) or non-reactive (negative) rapid test results may require confirmatory laboratory testing (e.g., confirmatory serology or nucleic-acid testing) as per local/regional guidelines. Always follow the manufacturer's Instructions For Use (IFU) and local regulations when performing and interpreting results.

