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 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

Autozyme Alkaline Phosphatase 60 Diagnostic Reagent (Pack Size : 12 x 5 ml) from Accurex. Alkaline Phosphatase 60 are used in the diagnosis of hepatobiliary disorders and bone disease associated with increased osteoblastic activity. Alkaline Phosphatase high levels may be a sign of a liver problem or a bone disorder Alkaline Phosphatase 60 reagent is set for determination of Alkaline Phosphatase activity based on kinetic method using p-nitrophenyl phosphate (p-NPP), the reagent is a Highly stable reagent & its activity can be determined in just 2.5 minutes. About Autozyme Alkaline Phosphatase is a reagent set for determination of Alkaline Phosphatase activity based on kinetic method using p-nitrophenyl phosphate (p-NPP) Autozyme Alkaline Phosphatase is a single reagent system using one step procedure Autozyme Alkaline Phosphatase has one step reconstitution. It involves dissolving substrate tablet in diluent Autozyme Alkaline Phosphatase is a Highly stable reagent Autozyme Alkaline Phosphatase activity can be determined in just 2.5 minutes Pack Size : 12 x 5 ml Principle The working solution is stablə for 21 days at 2- 8°C. The working solution should be prepared and stored in the dark (working solution bottle) provided.This is critical because the reagent is light sensitive. It should therefore be kept away from direct light. Alkaline Phosphatase cleaves p-nitrophenyl phosphate (p-NPP) into p-nitrophenol and phosphate. p-nitrophenol is a yellow color compound in alkaline medium and absorbs light at 405 nm. The rate of increase in absorbance at 405 nm. is proportional to Alkaline phosphatase activity in specimen. Quality Control To ensure adequate quality control, it is recommended that each batch should include normal and 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, temperature control, cleanliness of glassware and accuracy of pipetting. Other Details The kit should be stored at 2-8°C and is stable till the expiry date indicated on the label. The working solutions of Non Prostatic Acid Phosphatase & Total Acid Phosphatases are stable for 7 days at 2-8°C.

Infinite ADA 60 Diagnostic Reagent (R1 1 X 20ml: R2 1 X 10 ml) from Accurex. Infinite ADA reagent is used for direct quantitative determination of Adenosine deaminase (ADA) activity in human serum, plasma and other body fluids. The Reagent is a ready-to-use two liquid reagent system & can be performed in 11 minutes at 37° C. ADA is also know as Adenosine Deaminase which eliminates a molecule called deoxyadenosine, which is generated when DNA is broken down. About Infinite ADA is a reagent set for direct quantitative determination of Adenosine deaminase (ADA) activity in human serum, plasma and other body fluids. Infinite ADA is a ready-to-use, two liquid reagent system. With Infinite ADA, the assay is linear upto 200 U/L. Infinite ADA assay can be performed in 11 minutes at 37° C. Principle ADA catalyzes deamination of adenosine to inosine which is then converted to hypoxanthine by purine nucleoside phosphorylase (PNP). Hypoxanthine is then converted to uric acid and hydrogen peroxide (H2O2) by xanthine oxidase (XOD). H2O2 is further reacted with N-Ethyl-N-(2-hydroxy-3- sulfopropyl)-3-methylaniline (EHSPT) and 4-aminoantipyrine (4 AAP) in the presence of peroxidase (POD) to generate quinone dye. Quality Control To ensure adequate quality control, it is recommended that each laboratory should use a normal and an abnormal commercial reference control material. It should be realized that the use of quality control material checks both reagent and instrument functions together. Factors which might affect the performance of this test include instrument function, temperature control, cleanliness of glasswares and accuracy of pipetting. Other Details The reagents R1 & R2 are ready-to-use. The reagent kit should be stored at 2° – 8° C and is stable till the expiry date indicated on the label. Reagent R1 is light-sensitive & to be stored in dark. Contamination of the reagents should be strictly avoided.

Product Specification Model Name/Number i15 Brand Edan Usage/Application Laboratory Use Throughput Results In 1 Minute After Sample Aspiration Weight 3.65 Kg Battery 5000 mAh Rechargeable Lithium-Ion Battery Dimensions 238*153*310 mm (W x H x D) Display Type 7 Inch LCD Display Frequency 50 Hz Interface 4 USB 2.0 Host,1 RS232,WLAN Voltage 110- 240 V Input Device Touch Screen And Barcode Scanner Operating Temperature 10-30 Degree C Product Description Portable, lightweight Capable to run 50 samples with fully-charged battery Diagnose at the point of care, patient side, out in the Field or exam room Easy, Quick and Convenient Zero maintenance Minimize hands on time and training requirement Auto-sampling Report is ready within one minute after sample aspiration Accurate and Reliable Innovative microchip liquid control technology and micro-sensor multifunction membrane technology High sensitivity and accuracy Calibrator, Control and Electronic simulator to TRIPLE guarantee the RESULTS! Flexible Data Management Acquire patients' information via barcode/QR code Up to 10,000 patient data storage 4 USB ports and LAN/WiFi for data management Optional data management software Multi-parameter cartridge Multi popular time-sensitive parameters come in one cartridge, including ABG, electrolytes and metabolites Single-use cartridge avoids contamination Room temperature storage with long shelf-life

Overview A fully automated POC Auto Dry Biochemistry Analyzer called Mispa Chem Dx, With Just 3 to 4 drops (100ul) of whole blood to test up to 19 General and Special chemistry tests in less than 12 minutes. Mispa Chem Dx works on absorption spectroscopy where a change in absorbance is detected by an absorption spectrum and an algorithm is used to calculate the end concentration of the sample in the reagent dry disc. The reagent disc consists of lyophilized reagent beads, diluent, and calibration details in the QR code. The reagent disc contains an intelligent internal quality control system IQC which continuously monitors the disc function to ensure reaction stability and optimal disc performance, IQC is the engine that drives the Mispa Chem Dx accurately and precisely Low Sample Consumption Easy to Use Maintenance Free Accurate Result Disposable reagent disc Sample volume: 100µl Testing time: 12 minutes / sample Temperature: 37°C ± 0.3°C Resolution: 0.001Abs Absorbance: 0-3.0Abs Sample type: Heparinized whole blood, serum, plasma (heparin) QC&Calibration: IQC (Intelligent Quality Control/Calibration） Work condition: Temperature:10-30°C Humidity: 30%-70% Testing method: End point, kinetic, fixed time, turbidmetry etc Light source: 12V/20W, Halogen tungsten lamp with life span over 2500 hours Power supply: AC 100V-240V, 50-60Hz Display: Android 7.0 inch 800*480, multi-point capacitive touch screen Storage: 500,000 results Printer: Built-in thermal printer Interface: 4 USB ports, 1 LAN port Dimension: 315*375*475mm. 4.2kg(N.W.), 7kg(G.W.)

Cortisol Rapid Quantitative Test The Finecare™ Cortisol Rapid Quantitative Test is a fluorescence immunoassay for quantitative determination of Cortisol in human serum, plasma or whole blood. The test is used as an aid to the screening of adrenal dysfunction and assessment of the treatment effect. 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 The Finecare™ T3 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Triiodothyronine (total T3) in human serum, plasma or whole blood. The test is used as an aid to the assessment of thyroid function. 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 The Finecare™ T4 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Thyroxine (Total T4) in human whole blood, serum or plasma. The test is used as an aid to the assessment of thyroid function. 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.