The Watchline HIV–Syphilis Combo Rapid Test is a rapid, qualitative, in vitro diagnostic device intended for the simultaneous detection of antibodies to HIV-1, HIV-2, and Treponema pallidum (syphilis) in human whole blood, serum, or plasma


| TECHNICAL SPECIFICATIONS | |
| Test Technology | Lateral Flow Immunochromatographic Assay (LFIA) |
| Storage Condition | Store at 2°C – 30°C, Avoid direct sunlight |
| Target Analytes | HIV-1, HIV-2, and Treponema pallidum (syphilis) |
| Sample Type | Whole blood, serum or plasma |
| Shelf Life | 24 months |
| Sensitivity | 100% |
| Specificity | 100% |
| Regulatory Scope | ISO 13485 |