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SD BIOLINE Abbott HIV-1/2 3.0 test is an immunochromatographic assay for the differential and qualitative detection of all isotypes(IgG, IgM, IgA) antibodies specific to HIV-1 including subtype O and HIV-2 simultaneously, in human serum, plasma or whole blood.
Highly sensitive even to IgM during early infection stage
Differentiated test result between HIV type I and II by clear band formation(3-lines)
Specimen : Serum, Plasma (10uL), or Whole blood(20uL)
Sensitivity : 100%
Specificity : 99.8%
Clearance : KFDA, CE, WHO prequalification
24months at 1-30℃
Only For Clinical lab Supplies
No support will be provided to unqualified professionals
The Abbott BIOLINE HIV 1/2 3.0 is a professional HIV antibody screening test intended for use within an appropriate clinical or laboratory testing workflow.
A Reactive HIV screening result should not be treated as a final HIV diagnosis. HIV diagnosis requires completion of the applicable diagnostic testing algorithm, together with appropriate counselling, documentation and referral.
For clinical facilities, the value of rapid HIV screening is not only obtaining a result—it is ensuring that every result connects to the correct interpretation and follow-up pathway.
Rapid Diagnostic Tests for Gynecology & Antenatal Clinics: Pregnancy, HIV, HBsAg, HCV & Syphilis
This professional guide explains how pregnancy testing, HIV, HBsAg, syphilis and HCV screening can fit into gynecology, maternity and antenatal workflows, including result interpretation, documentation and referral principles.
HIV Rapid Test Kit Complete Guide
Understand HIV rapid-test principles, antibody and antigen detection, Reactive and Non-Reactive results, testing limitations and appropriate follow-up.
HIV Screening vs Confirmatory Testing: Why One Reactive Rapid Test Is Not a Final Diagnosis
A single Reactive rapid screening result should enter the appropriate HIV diagnostic pathway rather than being reported or interpreted as a stand-alone confirmed diagnosis.
HIV Testing During Pregnancy & Antenatal Care
HIV screening forms an important part of antenatal care. Appropriate testing, diagnosis, treatment and follow-up help protect maternal health and support prevention of mother-to-child transmission.
Rapid Test Do’s & Don’ts: HIV, HBsAg, HCV & Syphilis Sample Handling, Storage & Common Errors
Review essential professional practices covering specimen handling, kit storage, expiry checks, supplied buffers, timing, control interpretation, documentation and common rapid-test errors.
Professional-use note: Always follow the exact manufacturer Instructions for Use supplied with the current kit. Specimen volume, buffer quantity, timing, storage conditions and result interpretation are product-specific and should not be copied from another rapid-test brand or format.
| Specification name | Specification Value |
|---|---|
| Hiv test generation | 3rd generation |
| Product certifications & standards | CDSCO, CE certified |
| Test method | At-home test (self-administered), Point-of-care test, RDT |
| Test sample | Blood |