MICROLET®NEXT Lancing Device NEW SIMPLY IMPROVED The easy-to-use MICROLET®NEXT lancing device is designed to help minimize pain so you can test with confidence. New and Improved Features to Love: Locking endcap helps prevent accidental lancing 5 clearly visible depth settings Smooth-gliding mechanism to minimize noise Easy-to-use lancet ejector Uses silicone-coated MICROLET®lancets for smooth gliding into the skin Uses MICROLET®Lancets Silicone coated for easier, gentler testing Available in Seven (7) vibrant colours to allow colour coded testing Coloured lancets give you visual feedback to remind you to change your lancets more often

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

TACHOMETER/STROBOSCOPE, Model : BP-2259 ( 2 in 1, DIGITAL PHOTO TACHOMETER with DIGITAL STROBOSCOPE ) FEATURES* Intelligent, microprocessor circuit design, high accuracy, wide range, digital readout.* One instrument include two functions of " Digital Photo Tachometer " & " Digital Stroboscope "* Digital Stroboscope :Wide setting range from 100 RPM to 100,000 RPM, digital display with high accuracy. Modern solid state high visible orange light, long life, almost maintenance free. It is ideal for inspectingand measuring the speed of moving gears, fans, centrifuges, pumps, motors and other equipment used in general industrial maintenance, production, quality control, laboratories and as well as for schools and colleges for demonstrating strobe action.* Digital Photo Tachometer :No contact RPM measurement, wide measuring range from 0.5 to 100,000 RPM. 0.1 RPM resolution for the measured value < 1000 RPM. The last value, max., value, min. value can be stored into the memory automatically & be obtained by pressing " Memory Call Button ". High visible LCD display gives RPM reading exactly with no guessing or errors.* The use of durable, long lasting components, including a strong, light weight ABS plastic housing.Cabinet has been carefully shaped to fit comfortable in either hand. GENERAL SPECIFICATIONS Display 5 digits, 10 mm ( 0.4" ) LCD Operation 0 - 50 (32 - 122 ). ( Liquid Crystal display ) with Temperature function annunciation. Operating Less than 80% RH.Accuracy ± ( 0.1 % + 2 digit ). Humidity Sampling Time 1 second ( 60 RPM ). Size 215 x 65 x 38 mm.Time base:Quartz crystal. (8.5 x 2.6 x 1.5 inch). Circuit Exclusive one-chip design Weight 300g(0.66 LB)/including battery.microprocessor LSI circuit. Accessories : Carrying case ................... 1 PC.Battery 4 x 1.5V AA ( UM-3 ) battery. Operation manual ..............1 PC.ELECTRICAL SPECIFICATIONS ( PHOTO TACHOMETER )Measurement Range 5 to 99,999 RPM Resolution 0.1 RPM ( < 1,000 RPM ) 1 RPM ( 1,000 RPM )Photo Tach. detecting distance 50 to 150 mm/2 to 6 inch. * Typical max. 300 mm/12 inch depending upon ambient light.ELECTRICAL SPECIFICATIONS ( STROBOSCOPE )Stroboscopic 100 to 100,000 FPM/RPM Flash tube High efficiency orange LED Flash Rate FPM: flash per minute lamp.RPM : round per minute Flash Duration Approximately 60 to 1,000Flash Adjust 3 ranges : microseconds. Range Range A: 100-1,000 FPM Flash color Orange Range B: 1,000-10,000 FPM Flash Duration Approx. 16% of period time. Range C: 10,000-100,000 FPM Flash Adjust Coarse adjust knob and Resolution 0.1 FPM/RPM. Knob Fine adjust knob.(Less than 1,000 FPM/RPM) Calibration Crystal time base and1 FPM/RPM microprocessor circuit, don't(Over 1,000 FPM/RPM) necessary take any external calibration process. OPERATIONS PROCEDURES ( STROBOSCOPE )Preparation Determine the range switch to " 1000 RPM " ," 10,000 RPM " or" 100,000 RPM " position.Checking When checking speed, care must be taken to insure that the strobe is flashing in Speed unison (one to one) with the object being monitored. A Stroboscope will also stop motion at 2:1, 3:1, 4:1 et., this is normally referred to as harmonies. To be sure of unison, turn the dial until two images appear - this will double the actual speed. Then lower the flashing rate until a single and stationary image appears -this is the actual true speed.Checking For motion analysis, simply locate the actual speed as mentioned above and then Motion turn the dial slowly up or down. This will give a slow motion effect allowing complete inspection.

Product Details: Wavelength Range 195-1000 nm Display Digital Brand Thermo Sample Compartment 4 Position Cuvette Holder Interface RS-232C Packaging Type Carton Box We are the leading manufacturer of a wide range o These products are UV-VIS Spectrophotometer easy to operate and highly appreciated for its durability. Applications: Microprocessor based UVVIS Spectrophotometer is an analytical instrument that is commonly used in various physics & chemical laboratories to make qualitative and quantitative analysis of under focus materials in the presence of ultraviolet and visible spectrum range. It is widely used in fields such as clinical examination, medicine, petro-chemical industry, biochemistry, bio technology, quality control and environmental protection. It is also used in study at molecular level in of DNA and Proteins. It is non-destructive and easy to use in nature. Salient Attributes of the product: Cover 195 to 1000 nm 4 Position Cuvette Holder RS-232C Computer Interface High wavelength Precision Compact & Good Looking Shape Highly Accurate & Stable

Buy AccuTest HIV – 1/2 Ab Rapid Card Test (50 Tests) Online from Accurex. This Rapid HIV test is a visual, solid phase immunochromatographic assay for qualitative in-vitro diagnostic detection of antibodies against HIV-1 and HIV-2 in human serum/plasma. This HIV test may be used as an aid in diagnosis of HIV infection. In the HIV blood test – A reactive result should be confirmed by supplemental testing as part of a validated HIV testing algorithm. INTENDED USE: AccuTest HIV – 1/2 Ab test is a visual, solid phase immunochromatographic assay for qualitative in-vitro diagnostic detection of antibodies against HIV-1 and HIV-2 in human serum/plasma. The product may be used as an aid in diagnosis of HIV infection. A reactive result should be confirmed by supplemental testing as part of a validated HIV testing algorithm. INTRODUCTION: The Human Immunodeficiency Virus (HIV) is a retrovirus that infects cells of the immune system, destroying or impairing their function. The most advanced stage of HIV infection is Acquired Immunodeficiency Syndrome (AIDS). The general method of detecting infection with HIV is to observe the presence of antibodies to the virus by an EIA method followed by confirmation with any confirmation method. AccuTest HIV – 1/2 Ab is a simple, visual qualitative test that detects antibodies in human serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes. PRINCIPLE: AccuTest HIV – 1/2 Ab employs chromatographic lateral flow device in a cassette format. Colloidal gold conjugated recombinant antigens (Au-Ag) corresponding to HIV-1 (gp120 + gp41) and HIV-2 (gp-36) are dry-immobilized at the end of nitrocellulose membrane strip. HIV-1 & HIV-2 antigens are bound at the Test Zone (1 & 2) respectively. Goat Anti-Mouse IgG antibodies are bound at the Control Zone(C). When the sample is added, it migrates by capillary diffusion rehydrating the gold conjugate. If there are HIV-1 or HIV-2 antibodies in sample, they will bind with the gold conjugated antigens forming particles. These particles will continue to migrate along the strip until the Test Zone (1 or 2) where they are captured by the HIV-1 or HIV-2 antigens generating a visible purple line. If the specimen contains antibodies to HIV-1, the specimen will bind to the 1 test line and produce line. If specimen contains antibodies to HIV2, the specimen will bind to the 2 test line. If there are no HIV-1 or HIV-2 antibodies in sample, no purple line is formed in the Test Zone. The gold conjugate will continue to migrate alone until it is captured in the Control Zone (C) by the Goat Anti Mouse IgG antibodies aggregating in a purple line, which indicates that the migration of liquid has been successful. The control line must be present for the test to be valid. PRECAUTIONS: 1. For best results, adhere to instructions provided. 2. All specimens should be handled as potentially infectious. 3. The test device is sensitive to humidity as well as heat. 4. Do not use beyond expiration date. 5. Do not use test kit if pouch is damaged or seal is broken. 6. Use test device immediately after removing from the pouch. 7. The components (test device and assay diluents) in this kit have been quality control tested as a standard batch unit. Do not mix components from different lot numbers. 8. The AccuTest HIV – 1/2 Ab Test devices should be stored at 4 to 30 °C. Do not expose the kit to temperature over 30 °C. 9. Specimen with extremely high concentrations of red blood cells, fibrin should be recentrifuged before use. 10. AccuTest HIV – 1/2 Ab Test Device (Serum/Plasma) is for in vitro diagnostic use only. 11. AccuTest HIV – 1/2 Ab Test Device (Serum/Plasma) will only indicate the presence of antibodies to HIV-1/2 in the specimen and should not be used as the sole criteria for the diagnosis of HIV-1, HIV-2, and/or HIV-1 subtype O infection. 12. For confirmation of reactive test results, specimens should undergo further testing using different assays, such as rapid diagnostic tests, EIA and/or Western blotting in accordance with a validated HIV testing algorithm. 13. As with all diagnostic tests, all results must be interpreted together with other clinical information available to the physician. 14. Results should not be used to determine the serotype of HIV infections TEST PROCEDURE: 1. Allow the test device, buffer and specimen to reach room temperature (15-30 °C) prior to testing. 2. Remove the test device from the foil pouch and use the test device as soon as possible (within one hour). 3. Place the device on a flat, dry surface. Label with specimen ID. 4. Holding the sample dropper vertically above the test disk, slowly transfer 1 drop (10µl) of sample in to the sample well, then add 2 drops of assay diluent (about 75 µl) and start the timer. 5. As the test begins to work, you will see purple color moving across the result Window in the center of the Test Disk. 6. Wait for the colored lines to appear. Interpret test results at 15 to 20 minutes. Do not interpret test result after 20 minutes. STORAGE AND STABILITY Store as packaged in the sealed pouch at 4-30 °C (storage in refrigerator is permitted). Do not store in the freezer. Protect the test kit from humidly. The test device is stable until the expiration date printed on the test kit and/or sealed test device pouch. Do not use beyond the expiration date. The test device must remain in the sealed pouch until use.

Buy AccuTest HBsAg Rapid Card Test (50 Tests) Online from Accurex. HBsAg means Hepatitis B surface antigen which is a protein on the surface of hepatitis B virus. It can be detected in high levels in serum during acute or chronic hepatitis B virus infection. HBsAg positive indicates that the person is infectious. The hbsag test kit is a one-step immunochromatographic assay based on the antigen capture, or Sandwich principle. HBsAg positive treatment may include Antiviral medications. AccuTest HBsAg Card Test Hepatitis BHepatitis B is a viral infection that attacks the liver and can cause both acute and chronic disease. An estimated 240 million people are chronically infected with hepatitis B (defined as hepatitis B surface antigen positive for at least 6 months). Laboratory diagnosis of hepatitis B infection focuses on the detection of the hepatitis B surface antigen HBsAg. Hepatitis B surface antigen (HBsAg) consists of lipid carbohydrate and protein elements; the protein moiety provides a marker for identification of chronic, infectious BBV infections. Hepatitis B is transmitted sexually or intravenously and has an incubation period of six months. If not diagnosed properly and in time, it can develop into acute or chronic infection, liver cirrhosis and fulminant hepatitis. This test is very useful for screening blood donors, to find out whether they are HBsAg positive before collection of blood. Principle: AccuTest HBsAg is a qualitative test based on immunochromatography sandwich principle. The test card includes a combination of monoclonal anti-body gold conjugate (colloidal gold) and polyclonal solid phase antibodies which selectively binds Hepatitis B surface antigen with high degree of sensitivity. The HBsAg test is a one-step immunochromatographic assay based on the antigen capture, or Sandwich principle. The method uses monoclonal antibodies conjugated to colloidal gold and polyclonal antibodies immobilized on a nitrocellulose strip in a thin line. The test sample is introduced into well and flows laterally through an absorbent pad where it mixes with the signal reagent. If sample contains HBsAg, the colloidal gold-antibody (mouse) conjugate binds to the antigen, forming an antigen-antibody-colloidal gold complex. The complexes then migrate through the nitrocellulose strip by capillary action, which are stopped by an immobilized antibody zone forming a purple band. The formation of the first purple band (T zone) is indicative of hepatitis positive. To serve as a procedural control, an additional line of antibody antimouse IgG has been immobilized on the card. If the test is performed correctly, this will result in the formation of purple and upon contact with the conjugate as a control line. Safety Information AccuTest HBsAg test kit is designed lor detection of Hepalitis B Surface Antigenin the specimen. As with all diagnostic tests, il is recommended to interpret all the results in line wilh clinical manifestations, other lest resulls & clinicians’s view colleclively. If the lest device is showing stagnancy in flow on chromalography, it is most likely due lo problem in the sample. In this case, relest with a fresh sample or diluted sample. Direction for Use Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (25 ul), wait for few seconds till the Whole blood absorbed by sample pad (approx. 30 second), 4. Add 2-3 drops of buffer (60 ul) into the sample well. (If needed add one more drop of assay buffer). 5. Let reaction proceed until the appearance of positive line and control line or up to 20 minutes. 6. Read results after 20 minutes, strong positive reaction may visible within 5 minutes. 7. If negative or questionable results are obtained, the HBV infection is suspected, the test should be repeated ona fresh serum specimen. Storage: AccuTest HBsAg should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch.

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.

HumaScope ClassicLED is Particularly suitable for remote health care settings: Rechargeable battery allows for independence from constant power supply up to 5 days LED illumination: no replacement bulbs required Objective - Semi-Plan achromatic 4x, 10x, 40x, 100x (oil Immersion) Head – Binocular, Compensation Free Eyepiece – Widefield, 10x /18mm, Diopter Adjustment Revolver – Five Positions Reverse These are microscopes for education and routine laboratory applications; they are high-performing, durable imaging systems at affordable prices. They have robust mechanical construction combined with brilliant optics and latest LED technology as well as battery operation mode, making them first choice for health care settings especially in remote areas.

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