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'lgm ab'

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HEMOGLOBIN METER

Mispa HbX Portable Haemoglobin Analyzer Overview Mispa HbX , Smart Haemoglobin analyzer is a symbol of advanced point of care equipment with modern technology and convenience, designed to deliver high accuracy, quality results with least turnaround time and low maintenance. Best in Class Hemoglobin Meter Mispa HbX, the Smart Haemoglobin Analyzer, is the best example of an advanced point-of-care hemoglobin reader with modern technology. It is easy to use and designed to deliver accurate, high-quality results with the shortest turnaround time and minimal maintenance. This digital Hb meter is one of the best hemoglobin meters available. Working of A Hemoglobin Meter or a hemoglobin reader A hemoglobin meter or a hemoglobin reader measures the amounts of hemoglobin and hematocrit in whole blood. Hemoglobin tests are typically performed to determine the RBC count, the severity of anemia, hematocrit, and other haematological factors. It is widely utilized during blood donations and key decisions such as blood transfusions. HbX works with Spectrophotometry Scattered compensation Technology for accurate and quick results Results will be retrieved with in less than 3 seconds after sample reading starts Sample Required: 7ul Capillary or Venous blood Three Step procedure makes HbX more convenient to use CV value will be less than 1.5 % 6 Hours Battery Backup makes it a hand equipment 2000 Data storage capacity Micro Fluidic cuvettes with 2 year Shelf life

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immunoassayReagents

H-FABP Rapid Quantitative Test Finecare™ H-FABP Rapid Quantitative Test is a fluorescence immunoassay for quantitative measurement of Heart-type Fatty Acid Binding Protein (H-FABP) in human whole blood, serum or plasma. It is used for diagnosis of myocardial infarction.With original qualify control. STORAGE AND STABILITY 1. Store the test kit at 4℃~30℃ up to the expiration date printed on package. 2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing. 3. Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened.

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Immunoassay Reagents

INTENDED USE The Finecare™ 2019-nCoV lgM/lgG Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for qualitative detection of IgG and IgM antibodies of novel coronaviruses (2019-nCoV) in human whole blood, serum and plasma specimen. Clinically, the test is to be used as an aid in the diagnosis of coronavirus infection disease (COVID-19), which is caused by 2019-nCoV. The test provides preliminary test results. Negative results cannot exclude the possibility of 2019-nCoV infection and they cannot be used as the sole basis for treatment or other management decision. STORAGE AND STABILITY 1. Store at 4-30°C in the sealed pouch up to the expiration date printed on the package. Do not freeze. 2. The test device should be used within 1 hour after taking out from the foil envelope. 3. Keep away from sunlight, moisture and heat. 4. Kit contents are stable until the expiration date printed on the outer box.

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Rapid Test

Intended Use HIV Ag & Ab Card (4th Generation) is a visual, rapid qualitative and sensitive solid phase immunochromatographic assay for the differential detection of HIV-1 p24 Antigen and Antibodies (IgM, IgG & IgA) to HIV-1& HIV-2 in Human Serum/ Plasma/ Whole blood (collected by venipuncture or Fingerprick). The test is a screening test for p24 antigen (HIV-1) and HIV antibodies (anti-HIV-1 & anti-HIV-2) and is for in vitro diagnostic use only. It is intended for screening of blood donors or other individuals at risk for HIV-1 & HIV-2 infection and for clinical diagnostic testing. It is a screening test for p24 antigen (HIV-1) and HIV antibodies (anti-HIV-1 & anti-HIV-2). The test is for in vitro diagnostic use only and is intended for screening of blood donors or others individuals at risk for HIV-1 and/or HIV-2 infection and for clinical diagnostic testing. Salient Features • Finger prick, rapid, visual and qualitative Immunoassay. • 4TH Generation Rapid test for differential detection of p24 Antigen & antibodies for HIV in serum/plasma /whole blood. • Ideal for Blood screening, detects sero-negative HIV Cases. • Use of gp-41, C terminus of gp120 for HIV-1 , gp-36 for HIV -2 antibodies and Anti-p24 for HIV p24 Ag detection. • Detection of Group ‘0’ & subtype ‘C’ of HIV-1, which is most prevalent in India. • Based on Immunochromatography Technique. • See through device for easy interpretation of results. • Sensitivity : 100 % & Specificity: 100% • Analytical Sensitivity of HIV p24 Ag : 100 IU/ml (traceable to p24 Antigen NIBSC Standard, U.K. Code No. 90/636) • Long Shelf life 30 months at 2-30°C • Convenient pack size: 25 T.

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