COBIO S50 is Fully Automated Urine Sediment Analyser. COBIO S50 is Automation of the "Gold Standard" manual microscopy! • Throughput - 50 sample/hours • Large (13.3') high-resolution touch-screen for viewing actual images • Each test is processed in 1 cuvette - no carry-over between samples • Just 1.5 mins testing time / sample • High-definition in-built cameras capture "whole view-field" images similar to HPF images of manual microscopy • Latest "deep learning AI" technology identify, classify, label and count each sediment particle - Fully automated sample preparation (sample mixing, centrifuging, preparation of homogenized layer) to minimize manual errors - Large touch-screen helps zoom-in / zoom-out to access and review images and easily access the menu. - Each test is processed in 1 cuvette – no carry-over between samples - Just 1.5 mins testing time / sample

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 Malaria Pf(HRP II)/Pv Rapid Card Test (50 Tests) Online from Accurex. This Malaria test is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. This Malaria parasite test kit has test strips coated with Monoclonal Anti-p LDH antibodies (test line Pv) specific to the lactate dehydrogenase of P. vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P. falciparum. AccuTest Malaria Pf(HRP II)/Pv is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. PRINCIPLE: AccuTest Malaria Pf (HRP II)/Pv test utilizes the principle of immuno-chromatography. It has the test strip coated with Monoclonal Anti-pLDH antibodies (test line Pv) specific to the lactate dehydrogenase of P.vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P.falciparum. As the test sample flows through the membrane assembly of the device after addition of the buffer solution, the colored colloidal gold, anti-pLDH antibody and the anti-HRP-II antibody conjugate complexes with the lysed blood sample. The Malaria antigens get immobilized on the respective test lines on the nitrocellulose membrane which leads to the formation of red/purple colored band/s. The un-reacted conjugate and unbound complex if any moves further on the membrane and are subsequently immobilized at the control “C” region forming a red/purple band. This control band serves to validate the test performance and should always appear. This test is intended for professional use and must be used by trained personnel. Related products Safety Information PRECAUTIONS: 1. For in-vitro diagnostic use only. 2. The device is sensitive to humidity as well as to heat. So, it’s very important to take out the device from the sealed pouch just before use. 3. Do not use the kit after the expiration date. 4. Dispose all the samples and kits properly after test, in accordance with GLP. 5. Do not pipette reagent or blood by mouth. Direction for Use Procedure: 1. Disinfect with alcohol swab 2. Punture by lancet 3. Collect blood upto marking on sample dropper Other Info STORAGE AND EXPIRATION: 1. AccuTest Malaria Pf(HRP II)/Pv test kit should be stored between 4 – 30ºC. 2. Expiration date of this kit is 18 months after its manufacture date.

Buy AccuTest H Pylori AB Rapid Card Test (50 Tests) Online from Accurex. The Helicobacter Pylori is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies to H.pylori in human Whole Blood/Serum/Plasma. H Pylori test provides an aid in the diagnosis of infection with H.pylori. H.pylori is implicated in the etiology of a variety of gastrointestinal diseases, including duodenal and gastric ulcer, non-ulcer dyspepsia and active and chronic gastritis. h pylori symptoms are an ache or burning pain in your stomach (abdomen), Nausea, Loss of appetite, Frequent burping, Bloating & Unintentional weight loss NTENDED USE The H.pylori Antibody Rapid Test Card is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies to H.pylori in human Whole Blood/Serum/Plasma. It provides an aid in the diagnosis of infection with H.pylori. INTRODUCTION H.pylori is implicated in the etiology of a variety of gastrointestinal diseases, including duodenal and gastric ulcer, non-ulcer dyspepsia and active and chronic gastritis. H.pylori infection is found in more than 90% of duodenal ulcer patients and in around 75% of all peptic ulcer sufferers. H.pylori infection is also more common in gastric cancer patients. The risk of gastric cancer has been estimated to be six-fold higher in H.pylori infected populations than in uninfected populations. H.pylori infections occur in human populations throughout the world. In developed countries, about 50% of the population may have H.pylori infection by the age of 60 years, while only 10-20% of adults in the third decade of life have it. Transmission is most probably by the fecal-oral or oral-oral route. Both invasive and non-invasive methods are used to diagnose H.pylori infection in patients with symptoms of gastrointestinal disease. Invasive methods include culture of gastric biopsy samples, histologic examination of stained biopsy specimens, or direct detection of the urease activity in the biopsy (CLO test). These methods need to obtain a biopsy sample by endoscopy.which is expensive,and usually results discomfort and risk to the patient.noninasive techniques include urea breath tests and serological methods. Urea breath test requires expensive laboratory equipment and moderate radiation exposure. Serologic tests are employed to detect antibodies as human immune response to H.pylori, for example the ELISA and the Western immunoblot. The H.pylori Antibody Rapid Test Card detect antibodies to H.pylori infection in human Whole Blood/Serum/Plasma. It is a noninvasive method and does not use radioactive isotopes. The test is easy to perform and requires no specialized equipment. Visual interpretation provides an accurate qualitative result. It is a useful on-site aid in the diagnosis of H.pylori infection. Diagnosis of H.pylori infection by antibody immunoassay can reduce the number of patients requiring endoscopy. PRINCIPLE The H.pylori Antibody Rapid Test Card is an immunoassay based on the principle of the double antigen-sandwich technique. During testing, a Whole Blood/Serum/Plasma specimen migrates upward by capillary action. The antibodies to H.pylori if present in the specimen will bind to the H.pylori conjugates. The immune complex is then captured on the membrane by the pre-coated H.pylori antigens, and a visible pink-purple line will show up in the test line region indicating a positive result. If antibodies to H.pylori are not present or are present below the detectable level, a pink-purple line will not form in the test line region indicating a negative result. To serve as a procedural control, a pink-purple line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred. Safety Information The H.pylori Antibody Rapid Test Card is limited to provide a qualitative detection. The intensity of the test line does not necessarily correlate to the concentration of the antibody in the blood. x The results obtained from this test are intended to be an aid in diagnosis only. Each physician must interpret the results in conjunction with the patient’s history, physical findings, and other diagnostic procedures. x A negative test result indicates that antibodies to H.pylori are either not present or at levels undetectable by the test. Direction for Use TEST PROCEDURE 1. Remove the test cassette from the sealed pouch and use it as soon as possible. 2. Place the test cassette on a clean and level surface. 3. For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma to the specimen well (S) of the test cassette, then start the timer. See illustration below. 4. For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood (approximately 30μl) to the specimen well(S) of the test cassette, then add 2 drops of buffer (approximately 70μl) and start the timer. 5. Read results at 15 minutes. Do not interpret the result after 20 minutes. Other Info STORAGE AND STABILITY x Store as packaged in the sealed pouch at 4-40℃. The kit is stable within the expiration date printed on the label. x Once open the pouch, the test should be used within one hour. Prolonged exposure to hot and humid environment will cause product deterioration.

Buy Xpress Gluco + Test Strips (Pack of 50 Strips) Online from Accurex Point of Care (POC) Diagnostics. The Sugar machine strips require a sample volume of 0.5 μL and taking just 5 seconds to return a test result. XPRESSGLUCO+ strips make the testing experience superior. These Glucometer strips are for self-testing by people with diabetes at home and health care professionals in a clinical setting to monitor glucose concentrations in capillary whole blood drawn from the fingertips, forearm, upper arm, palm, calf or thigh Accurex Blood Glucose test strips provide accurate results in just 5 seconds. XPRESSGLUCO+ Blood Glucose Test Strips are used with the XPRESSGLUCO+ Blood Glucose Meters. They are intended for self-testing by people with diabetes at home and health care professionals in a clinical setting to monitor glucose concentrations in capillary whole blood drawn from the fingertips, forearm, upper arm, palm, calf or thigh. They are for testing outside the body (in vitro diagnostic use only). Donot use them for diagnosis of diabetes or testing on neonates. Specification Glucose in the blood samples mixes with a special chemical in the test strip and produces a small electric current. The amount of current produced changes with the amount of glucose in the blood. The glucose meter measures the strength of the current and displays the results as a blood glucose level. Safety Information • Discard used test strips and lancets responsibly according to your local regulations. • Keep test strips vial away from children. A child could choke on the test strips. The test strips and their vial contain agents that may be harmful if swallowed. If they are swallowed, promptly see a doctor for immediate assistance. Do not change medication based on the test results without the advice of a physician or healthcare professional. Direction for Use • Prior to first use, ensure that the package is undamaged and closed. • Keep the test strip vial away from sunlight and in a cool, dry place between 5 – 40°C (41 – 104°F). Do not freeze it. • Store test strips in their original pack only. Do not put the test strips in any other container. • Use test strips immediately after removing from the package. • Do not use test strips after the expiration date. • Avoid getting dirt, food or water on the test strip. Do not handle test strips with wet hands. All parts of the test strip should be touched only with dry and clean fingers. • Do not perform blood glucose tests at a temperature below +10°C (50°F) or above +40°C (104°F), or above 85% relative humidity Other Info Each test strip is plasma-calibrated†, requiring a sample volume of 0.5 μL and taking just 5 seconds to return a test result. The test range is 20 to 600 mg/dL (or 1.1 to 33.3 mmol/L) with resolution at 1 mg/dL (0.1 mmol/L). †Plasma-calibrated: Test results produced on capillary whole blood samples by XPRESSGLUCO+ System are compared with the results of the corresponding plasma samples tested by the YSI 2300 Glucose Analyzer, calibrated by YSI 2747 Glucose Standard (a NIST traceable glucose standard). The margin of error of the YSI 2300 Glucose Analyzer measurement is 0.289 mg/dL when the blood glucose concentration is higher than 100 mg/dL, or 0.029 mg/dL when the blood glucose concentration is lower than 100 mg/dL. (1 mmol/L= 18 mg/dL).

PA50 is a semi-auto analyzer for quantitative determination of specific proteins in blood, urine samples, including HbA1c, HS-CRP, CRP, ASO, CYS-C, RF, mALB, D-Dimer, IgM, IgG, IgA, C3, C4, etc. It’s an ideal instrument designed for medium or small labs or backup analyzer in large labs. General Features 5.6-inch color touch screen Calibration by magnetic card Disposable cuvette, no carryover Can be extended more than 30 parameters Support LIS and barcode Less and easy maintenance Features and Specifications Proven method: Fixed time nephelometry Sample type: whole blood, plasma, serum, urine 5.6-inch touch screen operation with intuitive software Light source: Diode Laser, 650 nm wavelength Precision: CV ≤ 5% Support barcode scanner Memory: 100,000 results storage Built-in thermal printer, support auto & manual print Certified by NGSP (National Glycohemoglobin Standardization Program)

VES MATIC 5 is the next-generation automated module manufactured by Diesse Diagnostica (Italy), a highly advanced, Intelligent, Intuitive & Interactive Graphic user Interface for estimating ESR using EDTA samples. Product Features: Automated instrument for the determination of ESR directly from EDTA vacutainers Faster TAT by loading 216 sample tubes at a time Pediatric samples can be processed in microtainers Reliable results with Temperature correction facility Accurate results by eliminating manual HCT correction in Anaemic samples Real-Time monitoring of samples Detection of Lipemic, Hemolyzed, Coagulated samples Standardization in mixing with Inbuilt Mixer Analyser P. Code Product Name Pack size Vesmatic 5 165941 Next 5K Transponder 1x 5000 Vesmatic 5 165942 Next 10 K Transponder 1x 10000 Display - 19" Full HD (1920x1080) LCD with PCAP Touch Screen Peripheral Control - based on Everex distributed control system with peripheral motor control boards Operating system - Linux Analysis module - 89 Positions for Sample Tubes Sample Loading - up to 18 racks simultaneously Throughput - 190 samples per hour. First result after 28 minutes Walk away mode - Supported Continuous loading - Supported Sample mixing - with multiple 180° rotations of the tubes Collection of analysed samples - reinserted into the original loading rack LIS Connection - Multiple LIS connection protocols are available: ASTM / Proprietary Remote diagnostics - available via Ethernet connection. Printer -Alphanumeric with 58mm-wide thermal paper, 36 characters per line, speed 20 mm/sec. Imaging System - 2 high resolution cameras for sample identification and analysis; 1 standard camera for internal inspection Image processor - Dedicated Quad Core CPU with integrated GPU for real-time HD image processing of samples Temperature range in operation - from +15 to + 35°C; Storage from + 5°C to + 45°C Humidity range - from 20% to 80% without condensation Central unit - Quad core ARM Cortex A-53 CPU ARM Cortex A-53, 16 GB eMMC, 4 GB RAM Interfaces - 2 x RS232C, 2 Host USB, 1 Client USB, Ethernet Protection category - CLASS I Safety standard - EN 61010-1, EN 61010-2-081, EN 61010-2-101 EMC - EN61326-1 Installation category - II Mains voltage - 230VAC@50Hz; US/Canada: 110-120Vac@60Hz Electrical energy consumption - 420VA Fuse block - 2 x 5.0 AT (delayed) (5 x 20 mm) UL Dimensions (mm) - 850 (W) x 750 (H) x 830 (D) Weight - 80 kg

The NB350 neonatal noninvasive ventilator is specially designed for neonatal ventilation, equipped with comprehensive NIV modes to provide reliable non-invasive respiratory support to meet the various needs of neonatal respiratory management. EasySync™ Technology The patented EasySync™ technology analyzes multi-channel parameters including gas flow and pressure without additional sensors, enabling accurate detection of spontaneous breath and improving synchrony in SNIPPV. The EasySync™ technology leads to a good synchronization performance comparable to electrical activity of the diaphragm (Edi). IOC (Intelligent Oxygen Control) The oxygen saturation of neonates tends to fluctuate, requiring caregivers to frequently adjust ventilator’s FiO2 settings. IOC (Intelligent Oxygen Control) achieves a closed-loop FiO2-SpO2 control by maintaining the patient’s SpO2 within the predetermined range, which reduces the workload of caregivers and improves patient safety. Integrated SpO2 monitoring for neonates in real time.1 Automatically adjust FiO2 setting by adaptive algorithm.2 Steadily maintain the SpO2 of neonates within the preset target range. Comfortable and Reliable Patient-interface The specialized patient-interface for the NB350 comes with a variety of sizes to fit for different clinical applications and patients. The ergonomic design with soft, skin-friendly material fully enhances the comfort of neonates throughout therapies. Bonnet/Headgear The bonnet/headgear integrate a fixings lot (seat) for pressure generator to avoid misposition and disconnection of patient-interface. Skin-friendly and breathable bonnet/headgear. Durable headgear hook-and-loop fastener allows easy and quick re-adjustment of the patient-interface. Infant Jet™ Pressure Generator Adjustable nasal prong/nasal mask positioning to adapt different facial orientations. Specifically designed to facilitate Coanda effect, significantly reducing respiratory resistance. Related Articles

At Mindray, we pride ourselves on our dedication and experience in developing better solutions for small labs. Our new 3-part hematology analyzer is the culmination of that effort. It provides small labs with more confidence in results and less turnaround time. Features CBC+3-DIFF, 20 parameters +3 Histograms Throughput: up to 30 samples per hour 8.4 inch TFT touch screen Only three reagents needed Open vial sampling Large storage capacity: up to 50,000 samples Original QC, calibrators and reagents Automation Fully Automatic Instrument Name Hematology Analyzer Brand Mindray Differential Type 2-Part Usage/Application Clinical Number Of Chambers 1 Model Name/Number BC-10 Power Source Electric Voltage 240 V Frequency 50 Hz