NEWSKU-24-MV8P79SF-HJWS
Promed Hepatitis B Surface Antigen (HBsAg) Rapid Test Kit
Unit Price · Ex-Lagos
₦15,000
approx. $9.80 at today's rate
10 units available · MOQ 1 unit · Ships in 48hrs
× ₦15,000
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The Promed Hepatitis B Surface Antigen (HBsAg) Rapid Test Kit is a professional in-vitro diagnostic screening test designed for the rapid qualitative detection of Hepatitis B Surface Antigen in human blood specimens.
The kit supports preliminary screening for Hepatitis B virus (HBV) infection, providing healthcare professionals with a convenient and efficient testing solution in hospitals, diagnostic laboratories, clinics, health screening centres and community healthcare programmes.
The HBsAg rapid testing format uses immunochromatographic technology to detect the presence of Hepatitis B Surface Antigen through visible test and control lines. Testing can be performed without complex laboratory instruments.
The product is particularly useful for routine clinical screening, antenatal screening programmes, preliminary infectious disease investigations and other medically indicated Hepatitis B assessments.
The Promed HBsAg Rapid Test Kit is designed to simplify diagnostic workflows while supporting timely medical evaluation and follow-up testing where necessary.
Key Features
- Hepatitis B Surface Antigen detection: Designed to detect HBsAg associated with current Hepatitis B infection.
- Rapid screening: A product listing for the Promed kit advertises results within approximately 15 minutes.
- Qualitative results: Reports reactive or non-reactive screening outcomes.
- Immunochromatographic technology: Standard lateral-flow antigen detection.
- Simple interpretation: Uses visible control and test lines.
- No analyzer required: Standard rapid-test devices can be read without dedicated laboratory equipment.
- Professional applications: Suitable for hospitals, clinics and diagnostic laboratories.
- Single-use testing: Disposable diagnostic test format.
- Convenient operation: Supports point-of-care and laboratory screening when performed according to the package insert.
- Follow-up testing: Reactive results can be investigated using appropriate confirmatory diagnostic procedures.
