Buy AccuTest Vitamin D Rapid Card Test (10 Tests) Online from Accurex. The Vitamin D test kit consists of 25 AccuTest Vitamin D individually packed test, devices in foil pouches, 25 pipettes for collecting 10 ul of whole blood, 25 lancets, 1 Buffer Vial (Buffer 5 mL) with stabilizers and, thimerosal, 1 Package Insert. Vitamin D Fast test kit is a rapid chromatographic immunoassay for the semi quantitative detection of Vitamin D levels in human blood/serum. This Vitamin D test provides a preliminary screening test result. INTENDED USE AccuTest Vitamin D is a rapid chromatographic immunoassay for the semi quantitative detection of Vitamin D levels in human blood/serum. This assay provides only a preliminary screening test result. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. The performance characteristics of this assay have not been established in a pediatric population. PRINCIPLE AccuTest Vitamin D is based on the principle of a competitive enzyme immunoassay. The assay is based on the competition for 25-OH Vitamin D present in blood/serum sample and Vitamin D present on the test line for fixed number of antibody-gold conjugate. Depending upon the concentration of Vitamin D in blood/serum, there will be free antibody-gold conjugate molecules that will bind to Vitamin D on the test strip and will show a colored line in the test line zone. A control line is present in the test window to work as procedural control. PRECAUTIONS 1. For in vitro diagnostic use only. 2. The test is designed for use with human blood/serum only. 3. Reagents must be at room temperature (8⁰C – 30 ⁰C). 4. Do not use if test device packaging is open or damaged. 5. Do not use the product beyond expiration date. 6. Handle all specimens as potentially infectious. Proper handling and disposal methods should be used according to good laboratory practices. 7. Read test results for 10 minutes as required. Results may deteriorate and may not be consistent after 10 minutes. 8. In order to avoid variable results, mix the blood sample thoroughly. 9. A serum sample subjected to repeated freeze thaw cycles may give variable results Direction for Use PROCEDURE 1. Remove the cassette from the sealed pouch and place it on a hard flat surface with the view window facing up (use the cassette as soon as possible). 2. Using a micropipette, add 10 µl of whole blood or 5ul of serum sample directly into the rectangular specimen well (marked with Red drop) of the cassette. 3. Add 3 full drops of Buffer into the square buffer well of the cassette (Do not move the cassette after addition of buffer). 4. Let the cassette sit for 10 minutes and read your results immediately. Results may deteriorate after the 10 minute mark. Other Info STORAGE AND STABILITY The test device should be stored at 8 ⁰C – 30 ⁰C and will be stable until the expiration date stated on the package. The product is humidity sensitive and should be used immediately after being open. INTERPRETATION OF RESULTS Match the color of the test line with the chart provided.

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.

XL 1000 with the throughput of upto 1040 tests per hour is the ideal instrument for centralizing the complete biochemistry testing load on a single fully automated platform. Increased walk away productivity and less human intervention make it an ideal analyzer for large laboratories. Equipped with all necessary advanced features that one expects from a high end fully automated chemistry analyzer; sample loading through rack system, cooled calibrator and control carousel, low reading volume of 150 µL, diffraction grating with 15 wavelengths from 340 nm to 800 nm and user-friendly software, to optimize and reliably run the daily lab workload. XL 1000 is a "dream come true" workhorse for laboratories with increased workload and the perfect solution. Fully Automatic, Discrete, Patient prioritized, Random Access Clinical Chemistry Analyzer with throughput of 1040 tests/hour 3 Reagent capabilities 147 long life Hard Glass cuvettes Separate Carousel for STAT samples Onboard refrigeration for reagents Extensive database for storing patient data and Q.C. results Primary tube sampling with bar code identification 9 stage laundry for cuvettes wash 150 samples can be loaded at a time through rack system System Discrete, open, automated, random access, patient prioritized, 1/2/3 reagent system DISPENSING OF SAMPLES AND REAGENTS Sample volume: 2-60 µl (0.1 µl step), 70 µl with ISE Reagent volume: 120 µl – 550 µl 3 dispensing probes ( R1, R2/R3) equipped with liquid -level sensor and crash detector Auto-dilution of samples and calibrators Clot detection Samples Serum, urine, plasma, CSF and other Economy Minimum reaction volume: 180 µl Reusable reaction cuvettes Mixing System 2 independent stirrers 3 user selectable mixing speeds Quality Control 4 levels of control material can be used Levey-Jennigs graphs Twin Plot diagrams for monitoring of systematic and random error Reaction unit with wash station 147 reusable hard glass cuvettes Possibility of replacement of individual cuvette Wash station – cuvette rinsing and drying in nine-step procedure Automatic cuvette blank measurement before analysis Sample Autoloader 23 racks 115 sample positions on automatic autoloader Primary tubes 5, 7 and 10 ml, vacuum system tubes Barcode reader for sample identification 2 Reagent trays With 43 cooled position each Barcode reader for reagent identification 20 ml, 50 ml reagent containers, 5 ml tube with adaptor Option to use one reagent for several test simultaneously Stat Tray 45 positions Can be used for blank, controls, STAT samples Software Convenient user interface Connection to LIS Programmable auto-start from sleep mode including automatic daily maintenance Statistical methods of processing results Data export in selected format Measurement Monitoring Colour indication of sample analysis Possibility of monitoring the reaction in real time Reagent volume monitoring Informative reports on ongoing analyzer status

INTENDED USE The Finecare™ S100β Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of S100β in human serum, plasma or whole blood. The test is used as an aid to the assessment of the level of cerebral injury. STORAGE AND STABILITY 1. Store the test kit at 4 ~ 30 ℃ up to the expiration date printed on package. 2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing 3. Do not remove the Test Cartridge from the pouch until use. The Test Cartridge should be used within 1 hour once opened.

Intended Use Hepacard is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV). Salient Features Detects all the 11 subtype of HBsAg. Antigen Sensitivity- 0.5 ng/ml. No sample preparation required. See through Device for easy result interpretation. Shelf life-30 months at 2-30°C. WHO Evaluated with 100% Sensitivity.

Intended Use HIV Ag & Ab Card (4th Generation) is a visual, rapid qualitative and sensitive solid phase immunochromatographic assay for the differential detection of HIV-1 p24 Antigen and Antibodies (IgM, IgG & IgA) to HIV-1& HIV-2 in Human Serum/ Plasma/ Whole blood (collected by venipuncture or Fingerprick). The test is a screening test for p24 antigen (HIV-1) and HIV antibodies (anti-HIV-1 & anti-HIV-2) and is for in vitro diagnostic use only. It is intended for screening of blood donors or other individuals at risk for HIV-1 & HIV-2 infection and for clinical diagnostic testing. It is a screening test for p24 antigen (HIV-1) and HIV antibodies (anti-HIV-1 & anti-HIV-2). The test is for in vitro diagnostic use only and is intended for screening of blood donors or others individuals at risk for HIV-1 and/or HIV-2 infection and for clinical diagnostic testing. Salient Features • Finger prick, rapid, visual and qualitative Immunoassay. • 4TH Generation Rapid test for differential detection of p24 Antigen & antibodies for HIV in serum/plasma /whole blood. • Ideal for Blood screening, detects sero-negative HIV Cases. • Use of gp-41, C terminus of gp120 for HIV-1 , gp-36 for HIV -2 antibodies and Anti-p24 for HIV p24 Ag detection. • Detection of Group ‘0’ & subtype ‘C’ of HIV-1, which is most prevalent in India. • Based on Immunochromatography Technique. • See through device for easy interpretation of results. • Sensitivity : 100 % & Specificity: 100% • Analytical Sensitivity of HIV p24 Ag : 100 IU/ml (traceable to p24 Antigen NIBSC Standard, U.K. Code No. 90/636) • Long Shelf life 30 months at 2-30°C • Convenient pack size: 25 T.

Getein 1100 is used to measure the concentration of biomarkers in human whole blood, serum, plasma, urine, nasal swab, or saliva samples. The results can be used as an aid in clinical diagnostics of laboratory and point-of-care testing. It is applicable in Emergency, critical care (ICU, CCU), outpatient, cardiology, inpatient wards, clinical laboratories, etc.

With the built-in oxygen concentration monitoring system and effective cable management system, the HyPort R80 is capable of creating a reliable and streamlined ICU environment to ensure patient safety. Recovery The lighting system of the HyPort R80 aims to create a comfortable, near-natural light ICU environment to enhance patient recovery. 1234 1 Circadian Light Simulating 24-hour natural daylight change to reflect circadian rhythm. 2 Examination Light Up to 10,000 lux, 5-level adjustable illuminance meets various needs of head and abdominal examination. 3 Reading Light Effectively avoid invalid glare to meet the reading needs of rehabilitating patients. 4 Navigation Light Providing enough lighting with less glare for medical staff’s easy observation and intervention. Efficiency The HyPort R80 is a highly integrated bedside device management system that helps caregivers organize medical devices to meet various clinical needs. It makes efficient use of beside space with a series of easy-to-use designs, enabling a more efficient workflow for medical staff. Folding-shelf design Suitable for both portable ventilators and integrated ventilators. p46-s3-2-web Bag-valve-mask management Making sure bag valve mask is easy to access and ready for emergency situations anytime when needed. p46-s3-3-web Partition management The pump separation layout allows medical staff to easily identify infusion pumps and feeding pumps. p46-s3-4-web Smooth movement The advanced braking technology ensures stability of the column when moving. NextPrevious Variety The HyPort R80 has been designed to meet the demands of different ICU layouts to create a safer, more efficient and comfortable ICU environment with patient-centric design.ICU double room solution A Product Specification Usage/Application Hospital Brand Mindray Model Name/Number HyPort B80 Features 60 Degreepanel interface for easier plug-in of gas and electricity Color White Panel Interface 60 Degree Product Description Gas and electricity separated 60°panel interface for easier plug-in of gas and electricity Flexible movement of sliding and rotating of the distributions Additional accessories for better management of details Considerate lighting option Safer and more effective workflow Gas and electricity separated 60°panel for easier plug-in of gas and electricity Better management Customized drawer solutions Wire basket - dfferent size options available Cable management solutions

Operate with Ease In the modern busy clinical environment, ease of use is a fundamental requirement for all medical devices. With this in mind, the new SV600 ventilators enable clinicians to set and deliver ventilation therapies quickly and easily via the intelligent ergonomic design and flat user interface. PulmoSight TM Utilizes numerical and graphical displays to show real time resistance, compliance and the spontaneous breathing status. Combined with the dynamic short trend display clinicians are able to monitor and evaluate changes in the patient's pulmonary ventilation and initiate the appropriate therapies. User configurable UI The SV600 ventilators offer exceptional user flexibility. Users are able to configure frequently used parameter controls by making them quick access shortcut keys in the UI. Also the ventilation mode keys can be arranged in order of frequency of use. This enables you to customize device in your way making parameter adjustment easier and quicker. Graphic guidelines The new intuitive graphical display enables users to learn quickly how to navigate and locate mode and parameter controls, thereby reducing errors and improving efficiency. Minimal Maintenance Routine maintenance requires no tools. The new 'door design' means that no tools are required to perform regular routine maintenance of the oxygen sensors, water trap, fan dust filter, HEPA air intake dust filter, etc. This ensures your new device always remains clean and clutter free. Intelligent Decision Making Ventilation modes and decision-supporting tools like Intelligent Assistant are developed on the basis of clinical needs and professional guidelines to help medical personnel calmly make clinical decisions. An extensive range of ventilation modes Smart ventilation solution: AMV TM + IntelliCycle TM Emergency solution: CPRVTM Sequential treatment regimen: Non-invasive ventilation & high flow oxygen therapy Dual channel auxiliary pressure measurements Lung protection kit Expandable Capabilities Securing your devices future is reliant on being able to expand your devices capabilities by interacting or integrating new concepts and technologies. The new SV800 / SV600 ventilators allow just this. Continue the latest electronic software and hardware, your new device is ready to embrace new technological advancement with ease. Integrated neonatal module with tidal volumes as low as 2 ml Plug & Play modules , including SpO2, mainstream or sidestream CO2 Backup air supply in case of air supply failure Seamlessly connected to the hospitals clinical information system via the Mindray BeneLink solution or eGateway solution Brand Mindray Model Name/Number SV600 Patient Age Group Neonatal, Adult, Paediatric Mounting Type ICU Operating Type Automatic Display Full color 15.6 inch Resolution 1920x1080 pixel Compliance IEC 60601-1-2 for EMC