Buy AccuTest HCV Rapid Card Test (30 Tests) Online from Accurex. HCV means Hepatitis C Virus which is a is a small, enveloped, positive-sense, single-stranded RNA virus. Hepatitis C symptoms are fever, fatigue, decreased appetite, nausea, vomiting, abdominal pain, dark urine, pale feces, joint pain and jaundice. HCV test is a rapid Chromatographic Immunoassay work on principle of the double antigen sandwich technique, Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. AccuTest HCV Test is a rapid Chromatographic Immunoassay for the Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. Hepatitis C Virus (HCV) is a small, enveloped, positive-sense, single-stranded RNA virus. Antibody to HCV is found in over 80% of patients with well documented non-A, non-B hepatitis. Conventional methods fail to isolate the virus in cell culture or visualize it by electron microscope. Cloning the viral genome has made it possible to develop serologic assays that use recombinant antigen, multiple antigens using recombinant protein and/or synthetic peptides have been added in new serologic tests to avoid nonspecific cross-reactivity to increase the sensitivity of HCV antibody tests. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. 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 (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or quest Principle: AccuTest HCV Rapid Hepatitis C Virus Test (Serum/Plasma/Whole Blood) is a lateral flow chromatographic immunoassay based on the principle of the double antigen-sandwich technique. The membrane is coated with recombinant HCV antigen on the test line region of the device. During testing, the serum/plasma or W.Blood specimen reacts with HCV antigen coated particles. The mixture migrates upward on the membrane chromatographically by capillary action to react with recombinant HCV antigen or membrane and generate a colored line. Presence of this colored line indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that the correct volume of specimen has been added and membrane wicking has occurred. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. 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 (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Safety Information •Positive: If a distinct purple line is formed at the test one marked ‘T’ (Test Line) and the Control Zone marked ‘C’ (Control Line) the test result is positive, indicating the sample contains Hepatitis C antibody. The interpretation of test results (+ve for hepatitis) remains unchanged even if there is a difference in intensity of color in positive line and control line as is many a time found. •Negative: If a distinct purple line is formed only at the control zone marked ‘C’ (control line) the test result is negative • Invalid: A total absence of color in both © and (T) regions or no colored band appears on the control © region is an indication of procedure error and/or the test reagent has deteriorated. Repeat with a new test kit. 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 (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Other Info Storage and Stability AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch.

Since the company was founded, Mindray has been continuously exploring new ways to improve diagnostic confidence. Powered by the most revolutionary ZONE Sonography® Technology, Resona 7’s new ZST+ platform brings ultrasound image quality to a higher level by zone acquisition and channel data processing. As well as the premium level image quality, Resona 7 also enhances clinical research capabilities with the revolutionary V Flow for vascular hemodynamic evaluation, and the most intelligent plane acquisition from 3D datasets for fetal CNS diagnosis. Combining the most intuitive gesture-based multi-touch operation and all the essential clinical features, Resona 7 is truly leading new waves in ultrasound innovation. With core platform advantages of ZST+ The channel data based ZST+ is an extraordinary innovation, representing an ultrasound evolution. Transforming ultrasound metrics from conventional beamforming to channel data based processing, ZST+ is able to deliver multiple imaging advances: Advanced Acoustic Acquisition, Dynamic Pixel Focusing, Sound Speed Compensation, Enhanced Channel Data Processing and Total Recall Imaging. Advanced features V Flow V Flow (Vector Flow) is a novel approach for vascular hemodynamic analysis. V Flow uses color coded vector arrows to indicate the velocity’s magnitude and direction of blood cells. With ultra-high frame rates, it provides extremely accurate and angle-independent visualization of complex vascular hemodynamic profiles. With comprehensive data information, V Flow is the most valuable tool for vascular clinical research. resona-7-fig3-1-pc UWN+ Contrast Imaging UWN+ (Ultra-Wideband Non-linear Plus) CEUS enables the Resona 7 to detect and utilize both the 2nd harmonic and non-linear fundamental signals, generating significantly enhanced images, resulting in greater sensitivity of minor signals and longer agent duration with lower MI. Forwarding smart to clinical intelligence The Resona 7 elevates clinical intelligence with a complete solution that enables clinicians to manage both routine and advanced studies more efficiently,consistently, and accurately, from acquisition to calculation. As an example, Smart Planes CNS shows exceptional intelligence in accurate diagnosis and analysis of the fetal central nervous system (CNS) Smart Planes CNS Mindray’s exclusive pioneering technology positions the Resona 7 as the industry’s first ultrasound system to allow fully automatic and accurate detection of the most significant planes and frequently used measurements of fetal CNS, leading to intelligent diagnosis, improved throughput, and reduced user dependence. Smart Planes CNS provides a user-friendly tool that greatly improves scanning efficiency through increased accuracy coupled with automated operation. With a simple button click on a 3D fetal brain volume image, the standard CNS scanning planes (MSP, TCP, TTP and TVP) and a range of related anatomical measurements (BPD, HC, OFD, TCD, CM and LVW) are obtained immediately. Smart Face Acquiring an optimal view of the fetal face in 3D ultrasound is cumbersome and time-consuming. In some cases, it is impossible to get rid of the occlusions such as cord, placenta, uterus and extremities. The new Resona 7 with Zone Intelligence provides a fast and intelligent optimization for fetal face with simply one-touch. It can immediately remove occlusions in the volume data, eliminate unwanted noise information, and generate an optimal view of the fetal face with minimal effort. Ergonomics The Resona 7 is designed around you. Gesture-based operation opens up a new trend in cart-based ultrasound with an agile, smart, and intuitive user experience beyond your expectations. Gel warmer’s three level temperature and swiveling angle adjustment of the control panel delivers great patient comfort and user convenience.

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

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AL6000 Alcohol Breathalyser The AL6000 analyzes a breath sample to detect alcohol in the lungs. This reading is then converted to blood alcohol concentration (BRAC – mg/L). The AL6000 uses an advanced oxide semiconductor sensor to detect alcohol. The AL6000 is the first and only breathalyzer that features Pre-Calibrated Alcohol Sensor Modules to eliminate the need for recalibration. Just snap out, snap in and you’re ready to go! 1 x Custom carry pouch 2 x Free batteries 5 x Plastic mouthpieces The UK Drink Drive Reading is 0.35mg/l on the AL6000 Unit we supply. Product Specification Color White Packaging Type Box Display Type Digital Application Law Enforcement Agencies Model Semiconductor Sensor Models Display LED Display Type of Mouthpiece Replaceable Analyzing time 5 s Clearing time 10 s Power Supply 1pc 9V battery Indication 00 to 0 40C or 0 00 to 0 400EL or Ing/L Minimum Order Quantity 1

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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.

Product Description: Laura SMART is a simple, quick and compact solution for routine clinical laboratories, ambulances and para clinics. It helps in automated timing, measurement and evaluation of urine test strips. Product Features: Two measuring modes (Standard: 60 samples/h & Smart Timing:240 samples/h) Portable mode using batteries Calculation of Microalbumin & Creatinine ratio Easy operation via touchscreen Product Applications: Automated reading of Urine test strips avoiding subjective errors in visual reading System: Semi-automated Urine strip analyzer Type: Reflectance photometer Measuring System: Wavelengths – 470, 540, 650 nm Memory: 400 results Throughput: 60 tests/hr in Normal Mode & 240 testes/hr in Smart mode User interface: Color TFT LCD display Printer: Built-in Thermal Printer Certificates: CE Physical Dimensions: 230 X 127 x 110 mm Weight: 0.8 Kg Test Strips: DekaPHAN Laura & MicroalbuPHAN Laura Parameters: Specific Gravity, Leucocytes, Nitrite, pH, Protein, Glucose, Ketone, Urobilinogen, Bilirubin, Blood & Microalbumin, Creatinine Optical QC: Grey QC strip System Interface: Communication via RS232 & USB port Host Protocol: Uni-directional Sample Identification: Sample ID via keyboard entry, barcode reader Power source: AC 90-230V/50-60 Hz Power consumption: 20 W max./1 W standby