This material replaces the material S0003823 SDMal Ag Pf/pan wnonsafetylancet,30T/kit. But the product itself remains the same.
Indicative Price 18.00 USD
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General description:
Bioline Malaria Ag P.f/Pan test kit intended for the detection of Malaria infection in human blood specimen, indicating qualitative and differential diagnosis between HRP2(Histidine-rich protein II) specific to Plasmodium falciparum and pLDH (Plasmodium lactate dehydrogenase) specific to Plasmodium species (Pan) in human blood specimen. Bioline Malaria Ag P.f/Pan test is intended for professional use.

Technical specifications:
Technology: Lateral immuno-chromatographic test
Format: Cassette, 30 tests
Sample type: Whole blood
Sample volume: 5µl
Pf panel detection score: 94.0% at 200 parasites/μl
Pv panel detection score: 91.4% at 200 parasites/μl
False positive rate: 0.0% for clean negatives
False positive rate: 0.8% for Pf at 200 parasites/μl
False positive rate: 0.7% for Pv at 200 parasites/μl
Invalid rate: 0.0%
Reading time: 15-30 mins

Manufacturer product reference: Abbott Diagnostics Korea Inc., 05FK67

Items supplied with:
·Test cassettes, individually packed in foil pouch with a desiccant, 30
·Assay diluent vials (180µl), 30
·Specimen transfer devices, 30
·Alcohol swabs, 30
·Sterile nonsafety lancets, 30
·Dried swabs, 30
·Latex gloves disposable, 30x2 packs
·Instruction for use, 1

Items required, but not supplied:
Timer, container for biohazard disposables, micropipette

Shelf life:
24 months from the date of manufacturing; do not use beyond its expiry date.

Weight and Volume:
Estimated weight: 0.72kg
Estimated volume: 0.0026m3

Storage and transportation condition:
The test kit should be stored at 1°C to 40°C, protect against humidity and direct sunlight. Do not freeze reagents.

Packaging and labeling:
Primary packaging: All contents of Bioline Malaria Ag Pf/Pan with nonsafety lancet, kit for 30 tests
Secondary packaging: One kit Bioline Malaria Ag Pf/Pan with nonsafety lancet, 30 tests

General recommendations:
·For guidance on selection criteria for procurement of mRDTs, kindly refer this page
·Public reports of WHO prequalified in vitro diagnostic products
·Follow strictly manufacturer instructions for use of the test procedure (especially adherence to reading time).
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