BC-6800 Today, laboratories not only need more reliable routine CBC plus 5-part diff WBC testing by way of high processing speed, but are also looking for options that extend the analyzer's output in form of Reticulocytes, Nucleated RBCs, Fluorescent Platelet counts etc. for wider clinical application and research. On the other hand, they are restricted by limited budgets. BC-6800 can help to meet all these needs just perfectly and even exceed the expectations. Additional parameters for further clinical applications IMG(#,%) parameters provide information about immature granulocyte, including promyelocytes, myelocytes and metamyelocytes. HFC*(#,%) parameters represent high fluorescent cell population, such as blasts and atypical lymphocytes. RET(#,%) extend valuable help in the differential diagnosis and/or therapeutic monitoring of anemias. IRF is parameter concerning immature reticulocytes, which can assist in early diagnosis of anemia and monitoring the bone marrow response to therapy. InR*(#,‰) are parameters regarding infected red blood cell. The red blood cells may infected by plasmodium, which can cause malaria. * means research parameters SF Cube Technology SF Cube is a pathbreaking technology for reliable blood cell analysis, including WBC differential, Reticulocytes and NRBC with efficient flagging. After reaction with proprietory reagents, the targeted blood cells undergo 3D analysis using information from scatter of laser light at two angles and fluorescence signals. The 3D scattergram builds the power to better identify and differentiate blood cell populations, especially to reveal abnormal cell population undetected by other techniques. Minimizing interference to ensure more accurate results NRBCs are counted in a dedicated channel by SF cube method, which automatically corrects total WBC count and 5-part Diff results when NRBCs are detected. The Focusing Flow-DC method minimizes the interference traditionally encountered in DC technology to produce near gaussian histograms. PLT-O result avoids the interference from microcytic and fragmented RBCs, large platelets and/or platelet clumps by fluorescent stain, and enhances the results accuracy and sensitivity. High automation to minimize the workload Throughput for 125 tests/hour, autoloader for 100 sample tubes capacity Bi-directional LIS with HL7 or ASTM communication protocol Customizable re-exam rules allow users to define their re-exam criterion according to lab’s practice

Product Description: Medica Corporation’s EasyLyte® analyzer is a completely automated, microprocessor-controlled electrolyte system that uses ISE (Ion Selective Electrode) technology to make electrolyte measurements. The EasyLyte measures combinations of Na+, K+, in whole blood, serum, plasma, or urine. EasyLyte incorporates state-of-the-art electronics and an innovative ergonomic design that differentiates it significantly from competitors. The analyzer also stores quality-control data that is easily accessible. Patient histories are immediately retrievable for evaluation. EasyLyte analyzers combine simple yes/no prompted operation, low maintenance, and high reliability into one economical design. Product Features: EasyLyte is Easy to Use, Easy to Operate, Easy to Maintain The entire menu is driven by 2 simple buttons Results are displayed on LCD screen as well as printouts EasyLyte does 2 point as well as 1 point calibration Facility to analyze different type of samples: whole blood, serum, plasma ,urine samples EasyLyte has capillary and syringe sampling facility EasyLyte has auto probe wiping facility Analysis of electrolytes is done using 100ul of blood and 400ul of diluted urine Rate of analysis 55 secs per sample Analyzer is capable of storing 128 patients data with trilevel QC results Analyzer has modular plug in reagent pack system EasyLyte has facility for auto calibrations with a programmed interval of 4 hrs and also calibration on demand Analyzer has facility to upgrade to a walk away Electrolyte station by use of Auto Sampler It has a built in thermal printer and a RS 232 port for interfacing Product Applications: Sodium - Na, Potassium - K CLIA Classification: Moderate Complexity Sample Type: Whole Blood, Serum, Plasma or Urine Sample Size: 100 µL Whole Blood, Serum, Plasma, 60 µL capillary or 400 µL diluted (1:10) Urine Method: Direct measurement by Ion Selective Electrode (ISE) Measurement Range: Blood Urine Na+: 20 – 200 mmol/L Na+: 25 – 1000 mmol/L K+: 0.2 – 40 mmol/L K+: 1.0 – 500 mmol/L Cl-: 25 – 200 mmol/L Cl-: 25 – 500 mmol/L Li+: 0.2 – 5.0 mmol/L Ca++: 0.1 – 6.0 mmol/L pH: 6.0 - 8.0 Units Display Resolution: Na+: 0.1 mmol/L K+: 0.01 mmol/L Cl- : 0.1 mmol/L Li+: 0.01 mmol/L Ca++: 0.01 mmol/L pH: 0.005 units Test Time: Na/K Na/K/Cl Na/K/Li Na/K/Cl/Ca Analysis time (blood) 55 sec 55 sec 55 sec 60 sec Urine mode Yes Yes Yes No Analysis time (urine) 90 sec 90 sec 90 sec N/A EasySampler Yes Yes Yes No Capillary Samples Yes Yes Yes No Data Storage: Patient Results: up to 128 samples QC Results: up to 20 each Normal, Low, and High Calibration: Automatic or On-Demand Output: 128 x 64 pixel graphic display 24 column thermal printer Serial port (RS-232), EasySampler port Ambient Conditions: 15–32oC (60–90oF), <85% humidity Power: 100-240 VAC 50/60 Hz, 0.8A Size & Weight: 9.5”W x 16.5”H x 8.0”D (24 cm W x 42 cm H x 20 cm D) 13 lbs. (5.8 kg) Reagents used with this 'EasyLyte' CLIA Classification: Moderate Complexity Sample Type: Whole Blood, Serum, Plasma or Urine Sample Size: 100 µL Whole Blood, Serum, Plasma, 60 µL capillary or 400 µL diluted (1:10) Urine Method: Direct measurement by Ion Selective Electrode (ISE) Measurement Range: Blood Urine Na+: 20 – 200 mmol/L Na+: 25 – 1000 mmol/L K+: 0.2 – 40 mmol/L K+: 1.0 – 500 mmol/L Cl-: 25 – 200 mmol/L Cl-: 25 – 500 mmol/L Li+: 0.2 – 5.0 mmol/L Ca++: 0.1 – 6.0 mmol/L pH: 6.0 - 8.0 Units Display Resolution: Na+: 0.1 mmol/L K+: 0.01 mmol/L Cl- : 0.1 mmol/L Li+: 0.01 mmol/L Ca++: 0.01 mmol/L pH: 0.005 units Test Time: Na/K Na/K/Cl Na/K/Li Na/K/Cl/Ca Analysis time (blood) 55 sec 55 sec 55 sec 60 sec Urine mode Yes Yes Yes No Analysis time (urine) 90 sec 90 sec 90 sec N/A EasySampler Yes Yes Yes No Capillary Samples Yes Yes Yes No Data Storage: Patient Results: up to 128 samples QC Results: up to 20 each Normal, Low, and High Calibration: Automatic or On-Demand Output: 128 x 64 pixel graphic display 24 column thermal printer Serial port (RS-232), EasySampler port Ambient Conditions: 15–32oC (60–90oF), <85% humidity Power: 100-240 VAC 50/60 Hz, 0.8A Size & Weight: 9.5”W x 16.5”H x 8.0”D (24 cm W x 42 cm H x 20 cm D) 13 lbs. (5.8 kg)

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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Intended Use The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C virus in human serum or plasma. It has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigen. Salient Features Based on “Flow Through Technology”, which is similar to Elisa technology because of involvement of washing steps at various levels to enhance the specificity. Use of highly purified HCV antigens for Core, NS3, NS4, NS5 immobilized on the device. Detection of all the subtypes of HCV. Results within 3 minutes. In built quality control dot which validates the test. 100% Sensitivity & 98.9% Specificity as per WHO evaluation. Shelf life : 24 months at 2-8°C

ntended Use The 4th Generation DIAGNOS HCV BI-DOT is a visual, rapid, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C Virus in human serum or plasma. The 4th Generation DIAGNOS HCV BI-DOT has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigens. Salient Features Rapid ,visual 4th generation test. Based on Flow Through Technology. Use of unique combination of Core, NS3, NS4, NS5 antigen. Detects all the subtypes of HCV. Result with in 3 min. Shelf life : 24 months at 2-8°C. Sensitivity- 100 %. Specificity- 99.8 %.

Intended Use The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG,IgM & IgA) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only. Salient Features Rapid visual test ,based on Flow Through Technology. Differential detection of HIV-1 & HIV-2. Detection of group ‘O’ & subtype ‘C’. Use of envelop antigens gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2. 100% sensitivity & 100% specificity as per WHO Evaluation. Shelf life 24 months at 2-8°C Available in convenient pack sizes- 50 Tests and 100 Tests. Results within 3 minutes. No instrument required. In built quality control dot.

Intended Use The 4th Generation HIV TRI-DOT + Ag test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 p24 antigen and HIV-1 & HIV-2 antibodies (IgM,IgG & IgA) in Human Serum or Plasma. The test is a screening test for p24 antigen (HIV-1), 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. Salient Features Rapid visual test ,based on enzyme immuno assay & Flow Through Technology. Rapid test for simultaneous and differential detection of p24 Antigen & antibodies for HIV on the same device. Ideal for Blood screening: detects sero-negative HIV Cases. Use of gp-41, C terminus of gp120 for HIV-1 antibodies & gp-36 for HIV -2 antibodies. Detection of Group ‘0’ & subtype ‘C’ of HIV-1, which is most prevalent in India. Unique washing steps for clear Interpretation of Results. Evaluated by National Institute of Biologicals- 100 % Sensitivity & 100 % Specificity. Long Shelf life: 15 months at 2-8° C.