At Mindray we pride ourselves on our dedication and experience in developing better solutions for small labs. Our new line of 3-part hematology analyzers is the culmination of that effort. Compact yet powerful, full featured yet affordable, the BC-20s is what a 3-part analyzer should be. Features CBC+3-DIFF, 19 parameters+3 histograms Throughput:40 samples per hour Intuitive operation system with 8.4 inch TFT touch screen Open vial sampling 200,000 results storage with histograms Original QC, calibrators and reagents Product Specification Instrument Name Haematology Analyzer Model Name/Number BC20s Usage/Application Laboratory Brand Mindray Automation Fully Automatic Operation Mode Fully Automatic

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

The OnSite hCG Combo Rapid Test is a lateral flow chromatographic immunoassay for the early detection of pregnancy, by providing a quick direct visual test for the placental hormone, hCG in human serum, plasma and urine. It can be performed within 5-10 minutes by minimally skilled personnel, and without the use of laboratory equipment. The OnSite hCG Combo Rapid Test is not intended for quantitative results, nor for over the counter (OTC) sales. It is intended to meet all requirements for yielding rapid, easily read, qualitative results for the purpose of early pregnancy detection via assay of hCG, a placental hormone that may be present in human serum, plasma or urine. The hCG detection limit the OnSite hCG Combo Rapid Test is 12.5 mIU/mL in serum or plasma specimen, and 25 mIU/mL in urine specimen. It is designed for professional use only, and provides only preliminary analytical data. For a final diagnosis of pregnancy, a more specific alternative clinical method must be used to obtain a confirmed analytical result. Clinical accuracy: In comparison with a reference chemiluminecsence or ELISA, hCG detection is 100% sensitivity and 100% specificity in urine specimens 100% sensitivity and 99.5% specificity in serum specimens Analytical sensitivity: 100% positive detection rate at 12.5 mIU/mL in serum/plasma specimens and 100% positive detection rate at 25 mIU/mL in urine specimens Analytical specificity: no cross reactivity with 1,000 mIU/mL human luteinizing hormone (hLH), 1,000 mIU/mL human follicle stimulating hormone (hFSH), and 1,000 mIU/mL human thyroid stimulating hormone (hTSH) Dose hook effect: no dose hook effect was observed for hCG at concentrations up to 500,000 mIU/mL in urine specimens Interference: No interference was seen with 35 biological and chemical analytes commonly found in OTC, prescriptions or abuse drugs in urine or serum/plasma specimens, as well as pH 4-9 (see detail in the package insert) Shelf life: 24 month Kit box package: 1. Individually sealed foil pouches containing; a. One dip strip device b. One desiccant 2. One package insert (instruction for use) Tube package: 1. Strip Package 2. One desiccant 3. One package insert (instruction for use) CTK Products at a Glance Drugs.com: Overview of Human Chorionic Gonadotropin Inserts

The OnSite hCG Combo Rapid Test is a lateral flow chromatographic immunoassay for the early detection of pregnancy, by providing a quick direct visual test for the placental hormone, hCG in human serum, plasma and urine. It can be performed within 5-10 minutes by minimally skilled personnel, and without the use of laboratory equipment. The OnSite hCG Combo Rapid Test is not intended for quantitative results, nor for over the counter (OTC) sales. It is intended to meet all requirements for yielding rapid, easily read, qualitative results for the purpose of early pregnancy detection via assay of hCG, a placental hormone that may be present in human serum, plasma or urine. The hCG detection limit of the OnSite hCG Combo Rapid Test is 12.5 mIU/mL in serum or plasma specimen, and 25 mIU/mL in urine specimen. It is designed for professional use only, and provides only preliminary analytical data. For a final diagnosis of pregnancy, a more specific alternative clinical method must be used to obtain a confirmed analytical result. Clinical accuracy: In comparison with a reference chemiluminecsence or ELISA, hCG detection is 100% sensitivity and 100% specificity in urine specimens 100% sensitivity and 99.1% specificity in serum specimens Analytical sensitivity: 100% positive detection rate at 12.5 mIU/mL in serum/plasma specimens and 100% positive detection rate at 25 mIU/mL in urine specimens Analytical specificity: no cross reactivity with 1,000 mIU/mL human luteinizing hormone (hLH), 1,000 mIU/mL human follicle stimulating hormone (hFSH), and 1,000 mIU/mL human thyroid stimulating hormone (hTSH) Dose hook effect: no dose hook effect was observed for hCG at concentrations up to 500,000 mIU/mL in urine specimens Interference: No interference was seen with 35 biological and chemical analytes commonly found in OTC, prescriptions or abuse drugs in urine or serum/plasma specimens, as well as pH 4-9 (see detail in the package insert) Shelf life: 24 month Individually sealed foil pouches containi a. One cassette device b. One plastic dropper c. One desiccant One package insert (instruction for use) CTK Products at a Glance Drugs.com: Overview of Human Chorionic Gonadotropin Inserts CATALOG # PRODUCT QUANTITY SPECIMEN R1001C hCG Combo Rapid Test CE 30/kit S/Urine OTHER PRODUCTS YOU MIGHT BE INTERESTED IN.. CATALOG # PRODUCT QUANTITY SPECIMEN R1001S hCG Combo Rapid Test (Strip) CE 50/kit, 100/kit S/Urine

We are the Leading Supplier of Abbe Refractometer Rajdhani. In the Abbe'' refractometer the liquid sample is sandwiched into a thin layer between an illuminating prism and a refracting prism. The refracting prism is made of a glass with a high refractive index (e.g., 1.75) and the refractometer is designed to be used with samples having a refractive index smaller than that of the refracting prism. A light source is projected through the illuminating prism, the bottom surface of which is ground (i.e., roughened like a ground-glass joint), so each point on this surface can be thought of as generating light rays traveling in all directions. A detector placed on the back side of the refracting prism would show a light and a dark region. Over a century after Abbe''s work, the usefulness and precision of refractometers has improved, although their principle of operation has changed very little. They are also possibly the easiest device to use for measuring the refractive index of solid samples, such as glass, plastics, and polymer films. Some modern Abbe refractometers use a digital display for measurement, eliminating the need for discerning between small graduations. However, the user still has to adjust the view to get a final reading. The first truly digital laboratory refractometers began appearing in the late 1970s and early 1980s, and no longer depended on the user''s eye to determine the reading. They still required the use of circulating water baths to control instrument and fluid temperature. They did, however, have the ability to electronically compensate for the temperature differences of many fluids where there is a known concentration-to-refractive-index conversion. Most digital laboratory refractometers, while much more accurate and versatile than their analog Abbe counterparts, are incapable of readings on solid samples. In the late 1990s, Abbe refractometers became available with the capability of measurements at wavelengths other than the standard 589 nanometers. These instruments use special filters to reach the desired wavelength, and can extend measurements well into the near infrared (though a special viewer is required to see the infrared rays). Multi-wavelength Abbe refractometers can be used to easily determine a sample''s Abbe number.

Best Fully Automated Clinical Chemistry Analyzer – Sphera M from Accurex. This chemistry analyzer is made in Italy & provides Accurate, Precise and Rapid Testing Solution. Sphera M is a Compact, fully automated, open random-access analyzer. The Minimum reaction volume is 210 µl, Minimal < 1L/h water consumption, 80 reusable UV transmitting Bionex® plastic cuvettes, 8-step wash station. It has Removable refrigerated tray with 30 open reagent positions for 50 ml or 20 ml bottles. Multiple virtual reagent disks can be programmed. The Chemistry analyser also does Auto-wash of inner & exterior probe surface. QUALITY CONTROL & CALIBRATION QUALITY CONTROL: • Levey-Jennings plots and Westgard multi rules • Upto 3 QC levels per test • QC monitor and reports • Method statistics: Test counter, CV%, mean, graphical trend analysis CALIBRATION: • Method and reagent monitor (volumes, available tests, calibration, QC status) • Automatic pre-dilution for calibrators • Upto 8 calibrators per method • Auto recalculation of result using last calibration. UNIQUE SOFTWARE DESIGN AND ARCHITECTURE: • Software designed for touch screen use • Intuitive user interface • Continuous loading of samples and reagents • Random-access and STAT • Free choice of execution order • Extended walk-away capability • Results archive with cumulative charts • Programmable automatic start up routine • Multiple work lists INTERFACE: • Bi-directional LIS, ASTM, over ethernet port of the external PC • Positive identification of samples with internal barcode reader (optional) • Printing on any Windows 7®/8® compatible printer • Method defined washing programs SYSTEM PACKS FOR SPHERA™ Accurex has developed dedicated system packs for Sphera™. Our biochemistry reagents have been intensively evaluated and validated to achieve the highest performance in Sphera™. Accurex recommends the use of these system packs according to instructions and applications validated by Accurex. Safety Information 8-step wash station for thorough cleaning of each cuvette (Needles: 6 dispensing, 6 aspiration, 1 cleaning) • Two types of systemic and special washing solutions for removing obstinate probe residues Direction for Use QUALITY CONTROL • Levey-Jennings plots and Westgard multi rules • Upto 3 QC levels per test • QC monitor and reports • Method statistics: Test counter, CV%, mean, graphical trend analysis CALIBRATION • Method and reagent monitor (volumes, available tests, calibration, QC status) • Automatic pre-dilution for calibrators • Upto 8 calibrators per method • Auto recalculation of result using last calibration Other Info Accurex has developed dedicated system packs for Sphera™. Our biochemistry reagents have been intensively evaluated and validated to achieve the highest performance in Sphera™. Accurex recommends the use of these system packs according to instructions and applications validated by Accurex.

Fully Automatic Oscar Om 511 Hematology Analyzer, For Clinical, User Input: Touch Instrument Name Haematology Analyzer Usage/Application All Automation Fully Automatic Brand OSCAR Parameters CBC + 5 Diff Differential Type 5-Part Number Of Chambers 2 User Input Touch / Manual Number Of Parameters ALL Parameters Instrument Type 5 PART Cell Counter Model Name/Number OM-511 Type Of Blood Analyzer Fully Automatic Sample Mode All Method All Throughput 60 Samples Per Hour Display Digital Features Catalogs Attached Sample Volume 15ul Storage 1 Lac Results No. Of Reagents Used 2 Lyse 1 Diluent Accessories Keyboard ,Mouse ,Tubing Set ,Power Adaptor, Print Roll Calibration Automatic / Manual Chamber Type Double Chamber Depth Of Chamber 100un Detector Yes Dilution Ratio 1.0 Loading Pattern Manual Measuring Method Electric Impedance & Cytometric Measuring Principle Electric Impedance & Cytometric Measuring Range 2 SD Measuring Time 52 Sec Number Of Reading Channels 2 Number Of Squares 4 Operating Voltage 220 Power Supply 220 Reagent System Close with RFID Sample Type Whole Blood Slide Size 0.3un Test Volume 15ul Wavelength 546 Weight 20 Kg Zero Setting Blank Aperture Size RBC 80 , WBC 100 , Plt 60 Is It Portable Yes Measurement Range Mm Hr 60 Test Per Hour Portable Yes Reading Chambers 2 Direct Sample Yes Optical System Wavelength Optical Source Flow cell Height 470mm Point Of Care Yes Dimension 365x470x525mm Printer Yes - Internal Humidity 88% Operational Ambient Temperature 37% Atmospheric Pressure 85 kpa User Interface Yes Reliable Yes Minimum Order Quantity 1 Product Description Company : OSCAR MEDICARE PVT LTD Brand : OM-511 CBC 5 Part Hematology Products Specification : The Brand New Autometed 5-Part Differentials hematology analyzer. Try-angular laser scatter + flow cytometry for 5 Part WBC Counting. Whole Blood, Peripheral Blood, Pre-diluted blood. Throughput with 60 Samples / hour. 29 Parameters (Include 4 research Parameters 3 Reagents with orignal QC & Carlibrators

Automation Fully Automatic Differential Type 3-Part Number Of Chambers 2 Number Of Parameters Neu% ,Low WBC & PLT Model Name/Number Acumedica DH23 Type Of Blood Analyzer Blood cell counter CBC ANALYZER Sample Mode Whole Blood, Capillary, Pre-Diluted CBC hematology analyzer Automation Fully Automatic Differential Type 3-Part Number Of Chambers 2 Number Of Parameters Neu% ,Low WBC & PLT Model Name/Number Acumedica DH23 Type Of Blood Analyzer Blood cell counter CBC ANALYZER Sample Mode Whole Blood, Capillary, Pre-Diluted Method Electrical Impedance Throughput 60 sample Features Low WBC ,LOW PLT, LOW WBC & PLT Sample Volume 9ul Storage 200000 sample No. Of Reagents Used 2 reagent Chamber Type Double Chamber Product Description CBC hematology analyzer