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The Ultra HIV Card is described on this listing as a professional HIV-1/HIV-2 antibody screening test for use with the specimen types specified by the manufacturer.
Because this is an antibody screening assay, it should not be interpreted as an HIV p24 antigen test or as a fourth-generation HIV antigen/antibody assay.
A Reactive result indicates that the HIV screening assay has detected the marker it is designed to identify.
However:
Reactive HIV screening ≠ Final HIV diagnosis
A Reactive screening result should proceed through the applicable HIV diagnostic testing algorithm using additional appropriately selected assays.
HIV Screening vs Confirmatory Testing: Why One Reactive Rapid Test Is Not a Final Diagnosis
A Non-Reactive antibody test means HIV antibodies were not detected by that assay at the time of testing.
Testing performed soon after a possible exposure may occur during the diagnostic window period, before sufficient antibodies have developed for detection.
Therefore, recent exposure may require repeat or additional testing according to the test type, exposure timing and applicable clinical guidance.
HIV Rapid Test Kit Complete Guide
Understand HIV antibody screening, third-generation versus fourth-generation testing, Reactive and Non-Reactive results, diagnostic windows and professional follow-up.
HIV Testing During Pregnancy & Antenatal Care
HIV screening is an important component of antenatal care. Reactive screening results require appropriate diagnostic evaluation and linkage to care rather than interpretation from one screening assay alone.
Rapid Diagnostic Tests for Gynecology & Antenatal Clinics: Pregnancy, HIV, HBsAg, HCV & Syphilis
This professional guide places HIV screening alongside HBsAg, HCV, syphilis and pregnancy testing while maintaining separate interpretation and follow-up pathways for each infection.
Rapid Test Do’s & Don’ts: HIV, HBsAg, HCV & Syphilis Sample Handling, Storage & Common Errors
Review specimen handling, pouch integrity, expiry, storage, controls, timing, documentation and common procedural errors that can affect rapid-test reliability.
Professional-use note: Follow the exact current manufacturer Instructions for Use for specimen type, specimen volume, procedure, reading time, storage, controls and interpretation. A single Reactive HIV screening result should not independently be considered a confirmed HIV diagnosis.
Legal Disclaimer: this is an diagnostic product to be used in Lab/hospital by medical professional expert supervision only Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and cross verify with ELISA / PCR Methods at your diagnostic centre or referral diagnostic laboratory
| Specification name | Specification Value |
|---|---|
| Test method | RDT |
| Test sample | Blood |
