utozyme Albumin 300 Diagnostic Reagent from Accurex. Albumin 300 is used for determination of albumin in serum or plasma based on BCG method. Autozyme Albumin is a single reagent system which is ready to use, Albumin is linear up to 6 gm% & can be determined in 1 minute at room temperature. Serum albumin in the presence of Bromocresol-green under acidic condition forms a green coloured complex. Albumin normal range is 3.4 to 5.4 g/dL (34 to 54 g/L). About Autozyme Albumin is a reagent set for determination of albumin in serum or plasma based on BCG method Autozyme Albumin is a single reagent system, ready to use. Autozyme Albumin is linear up to 6 gm% Albumin can be determined in 1 minute at room temperature The shelf-life of Autozyme Albumin is 18 months Pack Size : 2 x 50 ml Principle Serum albumin in the presence of Bromocresol-green under acidic condition forms a green coloured complex, The absorbance of this complex is proportional to the albumin concentration in serum or plasma. Quality Control To ensure adequate quality control, it is recommended that each batch should include a normal and an abnormal commercial reference control serum,. it should be realized that the use of quality control material checks both instrument and reagent functions together. Factors which might affect the performance of this test include proper instrument function, cleanliness of glassware and accuracy of pipetting. Other Details The reagents are for in vitro diagnostic use. BCG reagent and standard should be stored at temperature indicated on the bottle label.

Autozyme Albumin 100 Diagnostic Reagent (Pack Size : 2 x 50 ml) from Accurex. Albumin reagent is used for determination of albumin in serum or plasma based on BCG method, can be determined in 1 minute at room temperature. BCG reagent and standard should be stored at temperature indicated on the bottle label. Accurex has gained considerable expertise in manufacturing & marketing of In-vitro Diagnostic reagents. Serum albumin in the presence of Bromocresol-green under acidic condition forms a green colored complex. Albumin normal range is 3.4 to 5.4 g/dL (34 to 54 g/L). About Autozyme Albumin is a reagent set for determination of albumin in serum or plasma based on BCG method Autozyme Albumin is a single reagent system, ready to use. Autozyme Albumin is linear up to 6 gm% Albumin can be determined in 1 minute at room temperature The shelf-life of Autozyme Albumin is 18 months Pack Size : 2 x 50 ml Principle Serum albumin in the presence of Bromocresol-green under acidic condition forms a green coloured complex, The absorbance of this complex is proportional to the albumin concentration in serum or plasma. Quality Control To ensure adequate quality control, it is recommended that each batch should include a normal and an abnormal commercial reference control serum,. it should be realized that the uSe of quality control material checks both instrument and reagent functions together. Factors which might affect the performance of this test include proper instrument function, cleanliness of glassware and accuracy of pipetting. Other Details The reagents are for in vitro diagnostic use. BCG reagent and standard should be stored at temperature indicated on the bottle label.

The SV300 is a state-of-the-art ventilator that's simple to configure, easy to operate, and versatile in use. It treats pediatric and adult patients with all acuity levels at ICUs and Intermediate Care. Adaptive With its comprehensive list of standard features, including the latest modes of ventilation, the SV300 is appropriate for all levels of patient acuity and in all care settings, from the patient's bedside to transport to another point of care. Comprehensive Equipped with functions that are usually found on intensive care ventilators, the SV300 comes with extensive ventilation modes and unique features that make it a top level ventilator. p84-s4-1 Volumetric CO₂ measurement p84-s4-2 Weaning indicators p84-s4-3 O₂ Therapy p84-s4-4 Intelli Cycle Thanks to the intuitive UI design of the SV300, each function is in logical order so that clinicians do not need to navigate a complex menu. In addition, both the valves and flow sensor support autoclaving. This safety concept is designed to meet the current clinical trends of protecting patients even under the most demanding conditions.

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.

The Resona I9, a general imaging ultrasound system with completely innovative features from inside out. All innovations are developed based on in-depth insights into complex clinical scenarios, providing accurate and timely answers as well as outstanding efficiency and a remarkable user experience. Unlimited Scanning Flexibility Beyond Imagination iConsole - Intelligent Control Panel • Intelligent and clinical exam-specific control panel layout with special E-ink keys • Breakthrough design with adaptive layout for different clinical scenarios Full-space Floating Control Panel Can be adjusted for better space utilization, Easily meet various scanning needs Thoughtful Design for Ultimate Convenience 23.8" bezel-less full-screen with large images for immersive experience Eye-protecting monitor with adaptive brightness adjustment 15.6" full-HD touch screen with intuitive interaction Short-cut switch of latest used probes and exams Bring Optimal Patient Care Immediately Just Fold Down and Go Minimum 1 meter height Easy transportation by MPV (Multi-Purpose Vehicle) for mobile service Bedside Exams Without Power Cables • Up to 4 hours continuous scanning • Auto indication of residual power when you grasp the right handle

The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Troponin I (cTnI) in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL. It can be performed within 15 minutes by minimally skilled personnel, and without the use of laboratory equipment. The OnSite Troponin I Combo Rapid Test is intended to be used by healthcare professionals as an aid in the diagnosis of acute myocardial infarction (AMI). Any use or interpretation of this preliminary test result must also rely on patient’s symptoms and the professional judgment of a physician. A more precise test method such as an instrument method must be used to confirm the test result obtained by this device. Normally the level of cTnI in the blood is very low. cTnI is released into the blood stream in forms of free cTnI and cTnI-C-T complex at 4-6 hours after myocardial cell damage. The elevated level of cTnI could be as high as 50 ng/mL during 60-80 hours after AMI and remains detectable for up to 10-14 days post AMI. Therefore, circulating cTnI is a specific and sensitive marker for AMI. Clinical performance: Relative Sensitivity: 95.8% (95% CI: 91.5-97.9%) compared to a reference CLIA Relative Specificity: 99.7% (95% CI: 98.8-99.9%) Analytical sensitivity: The detection limit of cTnI is 1.0 ng/mL or greater in serum, plasma or whole blood specimen Cross-reactivity: No cross reactivity with 10 µg/mL skeletal muscle TnI, 2,000 ng/mL cardiac muscle TnT, 20 µg/mL cardiac muscle Myosin Dose hook effect: No hook effect was observed for cTnI at concentrations up to 3,521 µg/mL Interference: No interference was seen with 20 mg/dl Acetaminophen, 20 mg/dl Acetylsalicylic acid, 10.5 g/dl Albumin, 20 mg/dl Ascorbic acid, 1,000 mg/dl Bilirubin, 20 mg/dl Caffeine, 800 mg/dl Cholesterol, 200 mg/dl Creatinine, 20 mg/dl Gentistic acid, 1,000 mg/dl Hemoglobin, 600 mg/dl Oxilic acid, 1,600 mg/dl Triglycerides Shelf life: 24 months Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample diluent (REF SB-R3002, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Insert MedlinePlus: Troponin Test Poster

Accu-Chek® Active blood glucose meter Personalised Diabetes Coaching Accurate, no coding, easy Item Description The Accu-Chek Active blood glucose meter packs many powerful features into a smaller size. No coding reduces handling steps, see test result averages up to 90 days, get alerts if your test strips are expired or if you’ve underdosed, re-dose within 10 seconds, set pre-and post-meal reminders to test, and more. Benefits and Features accurate: Accurate1 blood glucose measurement easy: No coding for even easier blood glucose monitoring easy-to-read display (new typeface) intuitive handling with just 2 buttons safe: Underdose detection visual double check 10 seconds re-dose option clever: Pre- and postmeal markers postprandial reminder 7,14,30 or now 90 day test averages USB interface for data transfer Remark: Previous Accu-Chek Active meter generations will be upgraded to no coding via black activation chip . Know more>> 1The Accu-Chek Active bGM system meets the DIN EN ISO 15197:2013 requirements (data on file, 2014). Additional specifications Meter type : Accu-Chek Active meter (Model GB) Catalogue no. / Serial no. : See type plate on the back of the meter Test principle : Determination of glucose in fresh capillary blood by reflectance photometry. Blood glucose values can be tested in whole blood or plasma. The meter displays blood glucose values corresponding to those in plasma. Measuring interval : 10-600 mg/dL Blood volume : 1-2 μl Measuring time : Test strip in the meter: approx. 5 seconds Test strip outside the meter: approx. 08 seconds Power supply : 1 battery (type CR2032) Battery life : approx. 1000 tests or approx. 1 year Automatic power-off : after 30 or 90 seconds depending on operating status Memory : 500 test results with time and date, as well as 7, 14, 30 and 90 days averages Temperature : During testing: +8 to +42°C During storage without battery: -25 to +70°C During storage with battery: -20 to +50°C Atmospheric humidity : During testing: up to 85% relative humidity During testing: up to 93% relative humidity Altitude: Sea level to 4000 m Dimensions : 97.8 x 46.8 x 19.1 mm Weight : Without battery: approx. 46 g With battery: approx. 50 g Display : 96-segment liquid crystal display (LCD) Interface : USB (Micro B) Safety class : III Electromagnetic compatibility : The Accu-Chek Active meter meets the electromagnetic immunity requirements and the electromagnetic emissions requirements as per EN 61326-2-6 and EN ISO 15197 Annex A. The chosen basis for electrostatic discharge immunity testing was basic standard IEC 61000-4-2. Performance analysis : Calibration and traceability: The performance data for the Accu-Chek Active bGM system was calibrated using venous blood containing various glucose concentrations. Reference values are obtained using the hexokinase method, which is calibrated using the ID-GCMS method. Accuracy performance : The Accu-Chek Active bGM system meets the DIN EN ISO 15197:2013 requirements (data on file, 2014). How to use Accu-Chek Active blood glucose meter Testing your blood glucose is an essential part of managing diabetes. The Accu-Chek Active blood glucose meter can help to make it convenient by giving you fast, hassle-free, and accurate results in 4 simple steps. Insert the glucose test strip Prick your finger with the lancet to draw out a blood drop. Carefully touch the blood drop onto the green field of the test strip. Read the blood glucose result.

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)

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