Fully automatic, easy to operate • Bichromatic optic system with 4 wavelengths • 8-channel optic fibre system, reading whole plate in 5 seconds • Large LCD display, Win CE compatible operating system • Touch-screen or external mouse • Large memory to store 500 test parameters and 10000 results • Plate shaking feature • Can perform up to 12 different tests in one plate • Built-in modem support for long-distance maintenance and software upgrade (optional) • Multi-forms in result output including patient comprehensive report (optional) Vessel: Standard 96-well microtiter plates, or strip trays Linear Measurement Range: 0.000-3.500Abs Calculation Modes: Single point calibration, uptake mode, point-to-point curve fit, polynomial regression, linear regression (log and linear), cutoff absorbance, multipoint absorbance Wavelengths: Standard 405,450,490 and 630nm (340-700nm) four free position for optional filters (300-800nm) Accuracy: +/- 1% Light Source: Tungsten lamp (8V/50W) Mixer: Variable time and speed Display: 120mm x 90mm LCD Input: Touch-screen or external mouse Printer: External printer Memory: 500 tests and 10000 results Interface: RS-232 and parallel port Processor: RISC processor Power Requirements: 110V-260VAC, 50-60HZ Dimensions: 450mm(L) x 330mm(W) x 140mm(H) Weights: 10kg Certification: ISO 9001

Product Description: The LisaScan EM Microplate Reader is an economical, compact and versatile 8 channel ELISA reader which can be adapted to various ELISA applications. It is India’s largest selling automated microplate ELISA reader Product Features: Wavelength Range: 400 to 750nm with a dynamic measurement range of 0.0 to 4.0 O.D 100 user-programmable test storage Inbuilt thermal printer for reports & graphs Auto self-check on start-up & external printer connectivity Compatible to various plate geometrics-96 well microplates ( Flat, U & V bottom) Wavelength selection: Monochromatic, bi-chromatic & multi-chromatic* Reading time 8 sec. for single wavelength using 8-channel optics User-friendly inbuilt operation software with 7000 sample test results storage User interface: High Resolution LCD display with 20 Keys Rugged waterproof & membrane panel Computer linked ELISA data management software - Eli-LIMS* CE marked Inbuilt shaking facility,Three Linear Speeds - Low, Medium and Fast Reports can be printed using internal thermal or external printer No need of manual calculations and documentation Documentation ease – Reports can even be stored using optional Eli-LIMS software Computer can be connected Extensive ELISA data management Product Applications: ELISA System type: Open System Plate types: 96 well plates Wells Type: U, V and Flat bottom wells Operating Modes: Absorbance Quantitative Qualitative Semi-Quantitative Kinetic Mode Measurement Modes: Continuous / Step Shaking Modes: Three Linear Speeds - Low, Medium and Fast. Time duration can be set Wavelength Selection: Monochromatic Bi-Chromatic Multi-Chromatic* (Maximum 4) Calculation Modes: Non-linear Standard Cut-off Index Formula Column Subtraction Linear Regression Point to Point Cubic Spline Linear – Log Blank Options: Blank, Control, Assay Validation equations Against Air, Well Plate, Column, Column-mean Row, Row mean Number of programmable standards / calibrators: Up to 10 standards /test Storage/ display/ printing of multi standard curves and cut-off equations for all parameters Test Programs: 100 totally “open” Test Programs Photometer: Measuring system: 8-Channel optical system Lamp Source: Tungsten Halogen with Lamp saver function Wavelength Range: 400 to 750 nm Standard Filters: 405 nm, 450 nm, 492 nm, 630 nm (Optional two filters 578 nm, 700 nm), 10 nm Band Pass Dynamic Range: 0.0 ~4.0 OD Photometric accuracy: < 1% at 2.5 OD at 450 nm Photometric resolution: 0.001 OD Linearity: <1% at 2.5 OD at 450 nm Measurement Time: SPEED : 8 Seconds single wavelength NORMAL : 17 Seconds single wavelength Display: High resolution Graphics LCD 320x240 pixels, LED Backlight, View area: 120x92 mm Keyboard: Rugged waterproof & membrane panel PC Communication: USB Based Protocol compatible with Eli-LIMS and TNW Built-in Thermal Printer: Built in High resolution, 384 dots per line, thermal Type with full graphics facility printer and option for connecting External Parallel Printer (or USB Printer using External Adaptor). Computer interfacing Software: Windows Based Software Eli-LIMS with data managemenOptional Windows Based Software with data management capabilities to store patient results, store/display calibration curve /QC curves. Reports on internal and external printers: Report generation for last 7000 Sample’s is viewed/printed/stored. Lab name in Print-out Lab name in Display Collated reports Print-out of Normal Range along with the result (on external printer only). Graphs can be printed on Thermal Printer Sorted by: Date I.D. Both by Date & I.D. Test Plate ID Online Help: At each step on-line help in each menu. Beeps and online instructions on erroneous entry. Special HELP key on keypad. Operating Temperature: 20˚ C to 40˚ C Storage Temperature: -10˚ C to 50˚ C Humidity: Max. 80% RH, non- condensing Power Supply: 16 V - 24.5 V DC using External Auto ranging SMPS adapter 115/230VAC ±10%, 50/60Hz., Max. 90 Watt. (CE & UL certified) Dimension: 502 mm X 369 mm X 216 mm Weight: 7 Kg

INTENDED USE The Finecare™ TSH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of thyroid stimulating hormone (TSH) in human whole blood, serum or plasma. This test is used as an aid to assist in the assessment of pituitary gland and thyroid function. 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.

INTENDED USE The Finecare™ Progesterone Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of progesterone in human serum, plasma or whole blood. The test is used as an aid to the track ovulation. 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.

INTENDED USE The Finecare™ Testosterone Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative measurement of Testosterone in human whole blood, serum or plasma. The test is to be used as an aid in the diagnosis of diseases related to abnormal testosterone levels. STORAGE AND STABILITY 1. Store the test kit at 4~30ºC up to the expiration date printed on the package. 2. If removed from refrigerator, allow the test to return to room temperature for 30 minutes before testing. 3. Do not remove the cassette from the pouch until ready to use. The test cassette should be used within 1 hour once opened.

The Finecare™ One Step D-Dimer Rapid Quantitative Test is a screening test with fluorescence immunoassay to be used along with Finecare™ FIA System for quantitative analysis of cross-linked fibrin degradation products containing D-Dimer in human whole blood or plasma. The test is used as an aid in detecting the presence and assessing the degree of intravascular coagulation or thromboembolic events including pulmonary embolism.

INTENDED USE The Finecare™ One Step cTnT Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay for quantitative determination of cTnT concentration in human venous whole blood, serum or plasma specimen. It is mainly used as an aid to the diagnosis of myocardial infarction. STORAGE AND STABILITY 1.Store at 4~30 °C up to the expiration date printed on the package. 2. Do not remove the Test Cartridges from the pouch until ready to use. The Test Cartridges should be used within 1 hour once opened.

Luteinizing Hormone (LH) URINE RAPID TEST For Qualitative Detection of Luteinizing Hormone (LH) Urine Rapid Test Type : Device Pack Size : 25 T

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