Autochem Ingeniious is a semi automated clinical chemistry analyser & has been designed to meet the demands of the research as well as laboratory staff. Compact ergonomic design which is ideal for use in small-to-medium-sized laboratory. In-built Peltier regulated incubation compartment Integrated Coagulation Testing Mode Single & profile wise testing facility Flexible calibration modes Direct access key to run tests Enhanced Patient Data Storage & Retrieval Daily & monthlty QC program Wash & Aspiration function can be controlled using External Keyboard (PS/2 keyboard) roduct Specification Automation Semi Automatic Brand ARKRAY Assays Clinical Chemistry Power Supply Input Voltage : 90-260 VAC, 50/60 Hz Reaction Cuvette Flow Cell Weight <10 kg Power 100 Watts Max Country of Origin Made in India

Semi Automated Clinical Chemistry Analyzer Product Description Autochem Ingeniious is a semi automated clinical chemistry analyser & has been designed to meet the demands of the research as well as laboratory staff. Compact ergonomic design which is ideal for use in small-to-medium-sized laboratory. In-built Peltier regulated incubation compartment Integrated Coagulation Testing Mode Single & profile wise testing facility Flexible calibration modes Direct access key to run tests Enhanced Patient Data Storage & Retrieval Daily & monthlty QC program Wash & Aspiration function can be controlled using External Keyboard (PS/2 keyboard) Autochem Ingeniious is a semi automated clinical chemistry analyser & has been designed to meet the demands of the research as well as laboratory staff. Compact ergonomic design which is ideal for use in small-to-medium-sized laboratory. In-built Peltier regulated incubation compartment Integrated Coagulation Testing Mode Single & profile wise testing facility Flexible calibration modes Direct access key to run tests Enhanced Patient Data Storage & Retrieval Daily & monthlty QC program Wash & Aspiration function can be controlled using External Keyboard (PS/2 keyboard)

Product Description: XL-640 with CRS is a random access, discrete, patient prioritized, fully automated clinical chemistry analyzer with autoloader designed to meet the needs of today’s modern clinical laboratories with high workload. Once samples are loaded, it is a complete walk-away system. XL 640 CRS is designed to operate smoothly over the long haul and to deliver consistent quality report. Product Features: Throughput of 400 tests/ hour (Photometric) and 640 tests/hour with ISE 56 Reagent Positions with On-board cooling for reagents 162 Sample positions with /Autoloader Separate probes for reagent R1 & R2 and dedicated probe for sample Clot detection for sample probe, Reflex testing and Serum Indices identification 72 permanent hard glass cuvettes with On-board Laundry Automatic dilution for high abnormal samples & Auto Rerun facility Extensive QC Programmes with Levy –Jennings Curve & QC rules. Automatic calculation for Mean SD & CV% Direct loading for primary tubes Touch screen User Friendly GUI with Bi-directional connectivity. System General System Type: Automated, Discrete, Random Access, Patient Prioritized Clinical Chemistry Analyzer with Autoloader Throughput: 400 photometric tests/hour & 640 tests/hour with ISE (*optional ISE with Na, K, Cl, Li) Analytical Methods: 1-Point, 2-Point, Rate-A, Rate-B, Direct Potentiometry(optional) Barcode Reader: Both for Samples & Reagents (Optional) Reactions Tray: 72 hard glass cuvettes Reaction Mixing: Dual Stirrer with variable speed Reading Volume: 180 µl On-Board Laundry: 6 stage cleaning, 2 stage drying Photometer: Multi-wavelength diffraction grating with 12 wavelengths (340, 376, 415, 450, 480, 505, 546, 570, 600, 660, 700 & 750 nm) O.D. Range: 0 - 3.0 Light Source: Halogen Lamp Detector: Silicon Photodiodes Water Consumption: < 14 liters/hour Programmable Parameters: Default system pack parameters + upto 99 user defined parameters, Unlimited profiles and unlimited calculation items Quality Control: Q.C. plot data with Q.C. Rules. Provision for lab mean. Twin plot. Caliberation: K- factor, Linear (1,2 point and multipoint) 4P and 5P Logit-log, Cubic spline,exponential, polynomial. On-board serial dilution for calibrator Power Requirement: AC 220 V ± 10 %, 50 Hz or AC 110 V ± 10 %, 60 Hz Power Consumption: 800 VA Dimensions: Approximately 897 mm (w) x 655 mm (D) x 1170 mm (H) Weight: Approximately 200 Kg Sample Handling Sample: Serum, Plasma, Urine, CSF, Whole blood, other Sample Unit: upto 162 positions for samples/STAT/calibrator/controls with Autoloader Sample Pipetting: 2-70 µl (adjustable in 0.1 µl steps) for biochemistry,70 µl fixed for ISE capacitance probe with liquid level sensing and vertical obstruction detection , clot detection and serum indices and Reflex Testing Auto Rerun: Repeat with same, increade and decresaed volume (upto 1:150) Sample Tubes/Cups: Primary tubes of 5 ml, 7ml and 10 ml and sample cups Reagent Handling Reagent Tray: 56 positions for reagents with on-board cooling Reagent Pipetting: R1: 60 - 300 µl (Adjustable in 1 µl step) R2: 0 or 10 - 300 l (Adjustable in 1 µl step) Capacitance probe with level sensing and vertical obstruction detection System Interface Analyzer-PC: USB PC- HOST Computer: Bidirectional TCP/IP and RS - 232 PC- Printer: USB Operating System: Windows based with Touch Screen User Friendly GUI Database: Unlimited Results

The Autochem Xact Pro is a Fully Automatic Random Access Clinical Chemistry Analyzer. It is a compact, benchtop analyser with throughput up to 200 tests per hour. First-in-Class On-board Warm-water Laundry System Probe with Collision-Protection System Multi function Probe which works as mixer also Probe with Capacitance based liquid level sensor Robust Multi-functional Software Intelligent" Mixing Arm Removable & flexible Sample - Reagent Disc with 40 Open position for reagent & samples respectively. DESIGNED FOR UNINTERRUPTED WORK FLOW OTHER FEATURES ROBUST MULTI-FUNCTIONAL SOFTWARE Probe with Collision-Protection System Both horizontal and vertical collision protection ensures that system re-starts testing after any unwanted physical intervention. This prevents wastage of reagents, saves test time and increases life of probe Multi functional Probe Probe has flexibility to work even as a mixer in case in-built mixer does not work Probe with Capacitance based liquid level sensor Probe with liquid level sensor checks and indicates the presence of adequate sample or reagent in the container before starting testing process. Thus prevents unwanted interruptions in testing process “Intelligent” Mixing Arm User defined, variable three level mixing speed ensure thorough mixing Accurate performance of regular and immunoturbidimetric assays Independent cleaning station for mixer which prevents carry-over ensuring high precision Removable & flexible Sample – Reagent Disc 40 Open position for reagent & samples respectively Facility to use primary & variable sample cup as well as non fixed position for Sample, Control, Calibrator & STAT samples Two bottle sizes of 18 mL or 5 mL with unique design to reduce reagent dead volume Optional internal Reagent & Sample barcode reader makes the operation user friendly & ensure correct result reporting Reaction tray 60 reusable plastic reaction cuvettes which is also scanned before performing the test which means less recurring cost without compromising on quality. To assure precise results Individual replacement of cuvette offer lower consumable cost REFLEX Testing Functionality Allows user to program Low & High panic value for a particular test which triggers auto-testing of assigned tests which ensures faster and comprehensive reporting Dynamic & Real-time display of Test Running Status for quicker decision making Running status of reagent tray, Sample tray & reaction tray Real-time monitoring of Reaction curve On board inventory management Real-time monitoring of reagent residual volume saves reagent cost & time In-built full QC Program Provision to run 3 levels of control with Levey Jennings graph which gives confidence in reporting with multiple rules (1SD, 2SD and 3SD) Reagent, Calibrator & Control lot monitoring User friendly Bi-Directional LIS Interface

Accu-Chek® Guide Blood Glucose Meter Surprisingly Clever Diabetes is complex. Your testing doesn’t have to be Item Description Diabetes is complex. Your testing doesn't have to be with the Accu-Chek® Guide blood glucose monitoring system. With a spill resistant SmartPack® vial, a strip that lets you place a small drop of blood anywhere along the end, and an app that automatically logs results to your phone, it's a surprisingly simple way to manage your diabetes. Benefits and Features Simple to log results without a paper logbook - automatically logs results right to a mySugr app on your smartphone Simple to take just one strip - spill-resistant SmartPack vial lets you take one and spill none Simple to dispose off used test strips - push-button strip ejector means you don't have to touch used strips Simple to see, day or night - strip port light for testing in daytime, nighttime or anytime Simple to be more accurate - delivers advanced 10/10 accuracy for reliable results you can trust1,2,3 Meter Specifications Models: Accu‑Chek Guide wireless blood glucose meter Serial number: Unique serial number etched into meter back Sample claims: Capillary: Yes Venous: ROW = Yes Arterial: ROW = Yes Non-fingerstick sample claim ROW: Palm, forearm, upper arm Measuring principle: FAD glucose dehydrogenase (GDH) Measuring time: Less than 4 seconds Measuring conditions: 4°C to 45 °C (39°F to 113 °F) Storage conditions: -25 °C to +70 °C (-13 °F to +158 °F) Hematocrit range: 10 to 65% Humidity range: 10 to 90 % Altitude independence: 0 to 3,094 m (10,150 ft) Memory capacity: Up to 720 measurements with date and time; 32 control measurements Test averages: 7, 14, 30 and 90 days Data transfer wireless connectivity: using Bluetooth Smart Low Energy Dimensions: 80 x 47 x 20 mm (L x W x H) Weight Approximately: 40 g with batteries Display: Large backlit LCD display with full-text capabilities Beep tone: Yes (factory setting ON) Batteries: (2) 3-volt lithium coin cell type CR2032 Auto power off: 15 seconds after removing a test strip; 90 seconds otherwise Blood volume: 0.6 μL Measuring range: 10 to 600 mg/dL Sample types: Capillary, venous, arterial and neonate Sample dosing: Capillary fill function; suitable for AST Test strip stability 18 months after production date: Test strips are stable (even after opening) until the expiry date printed on the test strip vial. Note: Test strip container must be tightly closed after each strip is removed. Storage temperature : 4 °C to 30 °C (39 °F to 86 °F)

Buy Accurex H12 Hemoglobin Test Strips Online – for better result & accuracy. These Hemoglobin strips are used with URIT Hemoglobin Meter, for the quantitative measurement of total hemoglobin in capillary and venous whole blood. These hb strips are to be used by health care professionals only, not to be used for patient self-testing. Accurex HB Test Strips come with a pack size of 50 strips. The Accrues test strip utilizes Dry Chemistry Colorimeter Method (Azido methemoglobin Method). Meter’s optical detectors automatically measure the change in the membrane Buy Accurex H12 Hemoglobin Test Strips Online – for better result & accuracy. These Hemoglobin strips are used with URIT Hemoglobin Meter, for the quantitative measurement of total hemoglobin in capillary and venous whole blood. These hb strips are to be used by health care professionals only, not to be used for patient self-testing. Accurex HB Test Strips come with a pack size of 50 strips. The Accrues test strip utilizes Dry Chemistry Colorimeter Method (Azido methemoglobin Method). Meter’s optical detectors automatically measure the change in the membrane Operation Principle: The test strip utilizes Dry Chemistry Colorimeter Method (Azido methaemoglobin Method). When a drop of whole blood is applied to the test spot on the strip, blood immediately disperses within the membrane, contacting the reagent. The meter’s optical detectors avtomatically measure the change in membrane reflectance. The intensity of reflectance is inversely proportional to the hemoglobin concentration. Blood Sample Collection: Fresh or EDTA-anticoagulated capillary or venous whole blood may be used. If an EDTA – treated sample is refrigeratted to come to the room temperature before testing. EDTA treated blood samples should be mixed using end to and inversions at least 8 times prior to use, and should be tested within 24nours Do not use the haemolytic sample anticogulants other than EDTA are not recommended for use. Caution: 1. Same as all diagnostic tests, hemoglobin test results should be evaluated with the specific patient’s condition. Any results demonstrating the inconsistency with the patient’s clinical status should be repeated or supplemented with additional test data. 2. Do not touch the test membrane by hand 3. H12 Hemoglobin Test Strips are one-off product, do not use again Storage & Preparation: 1.H12 Hemoglobin Test Strips should be stored at O C-30 C dry and dark places, 2 C – B C is the best storage environment emperatures recommended. Keep away from direct sunlight and heat, must not be frozen, If the container was stored in refrigerated before first use, please don’t take it back into the refrigerator again after first use. 2. H12 Hemoglobin Test Strips are ready to use. No additional preparation is required 3. Enclosed desiccants with lest strip. Remove only those strips needed for testing. The remaining lest strips should be resealed in their onginal container and used up in 3 months after first use. Do not use lest strips and throw away alter expiry date. 4. Use the strip immediately once taking it out af the container, otherwise the result will be incorrect 5. Do not fold or cut the test strip. 6. Used lest strips cannot be used again, dispose them as normal medical waste Direction for Use Operating Instructions: 1. URIT Hemoglobin Meter, H12 Hemoglobin Test Strip, Lancing Device, and disposable blood taking needle. 2. Test steps: 1) Turn the meter on and input the Code Card. Check the Code Card displaying on the meter to ensure it to match the Code Card printed on the lest strip container. Otherwise, the result is incorrect. 2) Massage the patient’s finger from the knuckle up to the tip to stimulate blood flow. Clean the sample area with alcohol and wipe it dry with a sterile gauze pad. 3) Insert the lest strip into the strip holder with the notched end in first and the hole facing up. 4) Puncture the skin on the lower side of fingertip with blood collection needle, and remove 13-15 TIL of whole biood with capillary or other micro blood collection apparatus. While waiting for the instrument to display the blood drop symbol, quickly add the drops to the test hole on the reagent sheet. Please make sure that the blood drop volume can completely cover the test hole but not overflow the test hole. 5) The meter starts the test automatically after the blood sample disperses Once the lest is in process do nol disturb or move the meter or test strip, or press any key. The test result will display within 12 seconds. Qualtiy Control Procedure: Use only H12 Hemoglobin Test Strip with QC substance to perform QC. The range of QC substance is the numerical range indicated on the label of the QCsubstance or test strips. When to do a QCtest: 1. Whenever you suspect that the meter or test strips are not working properly. 2. If your hemoglobin test results are not consistent with how you feel. Other Info Limitations of test Method: H12 Hemoglobin Test Strip is only suitable for testing fresh or whole capillary blood or whole venous blood containing EDTA anticoagulants. Do not use serum, plasma or arterial blood

Buy AccuTest Typhoid IgG/IgM Rapid Card Test (5 Tests) Online from Accurex. The Typhoid IgG/IgM Rapid Test is used for detection & differentiation of anti-Salmonella typhi (S. typhi) IgG and IgM in human whole blood / serum / plasma. This Typhoid test is used as a screening test and as an aid in the diagnosis of infection with S. typhi. Salmonella typhi bacteria causes typhoid Typhoid fever, typhoid symptoms symptoms are likely to develop gradually – appearing one to three weeks after exposure to the disease. There are various typhoid treatment & typhoid vaccine which can be opted after the detetction of Typhoid. Typhoid fever is caused by S. typhi, a Gram-negative bacterium. Worldwide an estimated 17 million cases and 600,000 associated deaths occur annually. Patients who are infected with HIV are at significantly increased risk of clinical infection with S. typhi. Evidence of H. pylori infection also presents an increased risk of acquiring typhoid fever. 1-5% of patients become chronic carrier harboring S. typhi in the gall bladder. The clinical diagnosis of typhoid fever depends on the isolation of S. typhi from blood, bone marrow or a specific anatomic lesion. In the facilities that can not afford to perform this complicated and time-consuming procedure, Filix-Widal test is used to facilitate the diagnosis. However, many limitations lead to difficulties in the interpretation of the Widal test. In contrast, the Typhoid IgG/IgM Rapid Test is a simple and rapid laboratory test. The test simultaneously detects and differentiates the IgG and the IgM antibodies to S. typhi specific antigen thus to aid in the determination of current or previous exposure to the S. typhi. PRINCIPLE The Typhoid IgG/IgM Rapid Test is a lateral flow immunochromatographic assay. The test cassette consists of: 1) a pink-purple colored conjugate pad containing recombinant S. typhi H antigen and O antigen conjugated with colloid gold (Typhoid conjugates) and rabbit IgG-gold conjugates, 2) a nitrocellulose membrane strip containing two test region (Test line M and G) and a control region (control line). The test line ‘M’ is pre-coated with monoclonal anti-human IgM for the detection of IgM anti-S. typhi, test line ‘G’ is pre-coated with monoclonal anti-human IgG for the detection of IgG anti-S. typhi , and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the cassette, the test specimen migrates by capillary action across the test cassette. Anti-S. typhi IgM if present in the patient specimen will bind to the Typhoid conjugates. The immunocomplex is then captured on the membrane by the pre-coated anti-human IgM antibody at test region ‘M’, forming a pink-purple line at ‘M’ region, indicating a S. typhi IgM positive test result. Anti-S. typhi IgG if present in the patient specimen will bind to the Typhoid conjugates. The immunocomplex is then captured by the pre-coated reagents on the membrane, forming a pink-purple line at test region ‘G’, indicating a S. typhi IgG positive test result. Absence of any pink-purple line at test region (M and G) suggests a negative result. The test contains an internal control (control line) which should exhibit a pink-purple line of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the test region. Otherwise, the test result is invalid and the specimen must be retested with another device. PRECAUTION 1. This package insert must be read completely before performing the test. Failure to follow the insert gives inaccurate test results. 2. Do not open the sealed pouch, unless ready to conduct the assay. 3. Do not use expired devices. 4. Bring all reagents to room temperature (15°C-30°C) before use. 5. Do not use the components in any other type of test kit as a substitute for the components in this kit. 6. Do not use hemolized blood specimen for testing. Wear protective clothing and disposable gloves while handling the kit reagents and clinical specimens. Wash hands thoroughly after performing the test. 7. Users of this test should follow the US CDC Universal Precautions for prevention of transmission of HIV, HBV and other blood-borne pathogens. 8. Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled. 9. Dispose of all specimens and materials used to perform the test as biohazardous waste. 10. Handle the Negative and Positive Control in the same manner as patient specimens. 11. The testing results should be read within 15 minutes after a specimen is applied to the sample well or sample pad of the device. Read result after 15 minutes may give erroneous results. 12. Do not perform the test in a room with strong air flow, ie. an electric fan or strong air-conditioning. Other Info STORAGE AND STABILITY Typhoid IgG/IgM test card should be stored at 4-40°C. The card may be stored at room temperature but not exceeding 40°C in the original sealed pouch. The shelf life or expiry of the card is printed on Pouch as well as carton label. The test kit should be kept away from direct sunlight, moisture and heat.

Buy the Best Automated Hematology Analyzers – Acculab CBC 360 Neo. This Hematology Analyser Machine is Truly Automated for self-checking, background test, calibration, sampling, dilution, mixing, printing, dormancy, alarms, cleaning and maintenance. CBC 360 Neo is 3 part hematology analyzer from Accurex & is Automated for Walk-away Operations. Dual Chamber: Measurement of RBC / platelets & WBC / HGB in different chambers ensure accurate counting in a short time. The micro-aperture sizes of both the chambers are well designed to avoid error due to cell misclassification Automation for Walk-away Operation: Auto Self-check : Automatic aspiration of reagents & rinsing of tubings on startup Auto Blank : Background test is run automatically on startup Auto Print : Automatic printing of report with / without histogram Auto Sleep : Dormancy status is entered after a set period of non-operation Auto Alarms : Audio / visual alarms in case of system errors & abnormal results Auto Clean : Automatic rinsing options available to maintain the system Dual Chamber: Measurement of RBC / platelets & WBC / HGB in different chambers ensure accurate counting in a short time. The micro-aperture sizes of both the chambers are well designed to avoid error due to cell misclassification Specifications: Measurement principle: Electrical resistance for counting RBC, WBC & Platelets Colorimetric estimation of HGB at 540 nm Parameters: WBC, LY, MO, GR, LY%, MO%, GR%, RBC, HGB, HCT, MCV, MCH, MCHC, RDW-CV, RDW-SD, PLT, MPV, PDW, PCT, P-LCR Throughput: 60 samples/hour Micro-aperture: WBC : 100 um RBC / PLT : 68 um Sample type: Whole blood or pre-diluted sample Sample volume: Whole blood (venous blood) : 10 ul Chamber: Pre-diluent (capillary blood) : 20 ul, Pre-diluent (capillary blood) : 20 ul Reagents: Dual chamber : RBC / Platelets & WBC / HGB Quality control: 4 QC options : L-J, X-B, X-R & X QC, Graphs plotted with 31 data points Data memory: Upto 100,000 (with histogram) Display: 10.4 inch LCD with 640 x 480 resolution Printer: Built-in thermal printer Interface: Support RS-232C, standard network port and USB; keyboard and mouse Operating environment: Temperature : 15˚C – 35˚C, Humidity : 85% RH Electrical specification: Voltage : AC 110V/230V 23V Frequency : 50/60 Hz, Power : 180W Fuse specification : 250V/3A Dimensions / Weight: 670 x 515 x 640 mm / 27.5 kgs Specification Acculab CBC 360 Neo – Fully Automated Hematology Analyzer Features: 3-part differentiation of WBC Automated for — self-checking, background test, calibration, sampling, dilution, mixing, printing, dormancy, alarms, cleaning and maintenance High processing speed : 60 samples/hour Multi-parameter estimation : 20 parameters categorized according to corpuscle type for easy reporting Direct command keys for Mode, Prime, Flush, Drain & Record / Print for faster operation Run / Standby indicator lights denote the analyzer status i.e. test is being run or analyser is ready to test Whole blood/ Pre-diluent indicator lights denote the sample type in use i.e. whole blood/ pre-diluent Dual sample mode with low sample volume: Whole blood (venous) mode : 10 ul; pre-diluent (capillary) mode : 20 ul Audio alarm indication for abnormal findings or system errors 4 QC methods : L-J, X-B, X-R & X QC Comprehensive QC graphs with 31 data points for each parameter Internal & external probe cleaning facility Dormancy mode available to reduce power consumption Memory : 100,000 (with histogram) Safety Information • Large 10.4 inch single screen color display of all 21 parameters and 3 histograms • Sequential arrangement of WBC, RBC & PLT parameters for convenient reporing •Easy to understand & icon-based arrangement of menu for fast and convenient testing Direction for Use • WBC Histogram: R1, R2, R3, R4 & RM indications on histogram show specific abnormalities in the histogram & the probable causes • Platelet Histogram: PM indication is given when the boundary between PLT & RBC is ill-defined thus avoiding misclassification Other Info High voltage cautery function is useful in disintegrating obstinate protein or serum clog in the tubing

Product Features: Better precision, CV < 2.5 % Patented CLE technology enables complete elimination of labile glycohemoglobin ensuring accurate HbA1c results. HbA1c test results in 3.5 minutes with HbA2/HbF flagging. Separation of hemoglobin fractions Complete removal of labile fraction up to 10% No interference of HbF up to 10% No interference of lipemia or icterus, can run on non-fasting patient samples HbA1c reportability presence of HbS, HbC, HbD and HbE Compact bench top model User friendly touch screen operation Sampling from multiple sized primary tubes, including microcapillary collection tubes On board QC functions with Levey-Jennings and statistical calculations Unlimited storage of calibration, QC data and chromatograms No sample preparation required Simple reagent and column replacement Automated maintenance RFID reagent identification and tracking Automatic barcode identification of samples NGSP certified Calibrators and Controls IFCC traceable Complete kit with buffers, calibrator and column Product Application: Hba1c Testing Sampler Handler: 10 Position Rack Loader, positive identification by internal barcode reader Sample Type: Whole blood on EDTA K3 or K2 anticoagulant Haemolysate from EDTA whole blood samples Time for Analysis: Throughput approximately 3.5 minutes between samples Interferences: Complete removal (not separation) of labile up to 10% Sampling System: Sample Aspiration Probe coupled with a high precision, Sample Aspiration Volume: 14.5 µl in whole blood, 670 µl in lysate mode. Pump: 2 high pressure syringe pumps Detector Type: UV-Vis Reagent Traceability: RFID Printer: Built- in thermal printer with possibility to connect to external printer