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.

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.)

BC-6800 Today, laboratories not only need more reliable routine CBC plus 5-part diff WBC testing by way of high processing speed, but are also looking for options that extend the analyzer's output in form of Reticulocytes, Nucleated RBCs, Fluorescent Platelet counts etc. for wider clinical application and research. On the other hand, they are restricted by limited budgets. BC-6800 can help to meet all these needs just perfectly and even exceed the expectations. Additional parameters for further clinical applications IMG(#,%) parameters provide information about immature granulocyte, including promyelocytes, myelocytes and metamyelocytes. HFC*(#,%) parameters represent high fluorescent cell population, such as blasts and atypical lymphocytes. RET(#,%) extend valuable help in the differential diagnosis and/or therapeutic monitoring of anemias. IRF is parameter concerning immature reticulocytes, which can assist in early diagnosis of anemia and monitoring the bone marrow response to therapy. InR*(#,‰) are parameters regarding infected red blood cell. The red blood cells may infected by plasmodium, which can cause malaria. * means research parameters SF Cube Technology SF Cube is a pathbreaking technology for reliable blood cell analysis, including WBC differential, Reticulocytes and NRBC with efficient flagging. After reaction with proprietory reagents, the targeted blood cells undergo 3D analysis using information from scatter of laser light at two angles and fluorescence signals. The 3D scattergram builds the power to better identify and differentiate blood cell populations, especially to reveal abnormal cell population undetected by other techniques. Minimizing interference to ensure more accurate results NRBCs are counted in a dedicated channel by SF cube method, which automatically corrects total WBC count and 5-part Diff results when NRBCs are detected. The Focusing Flow-DC method minimizes the interference traditionally encountered in DC technology to produce near gaussian histograms. PLT-O result avoids the interference from microcytic and fragmented RBCs, large platelets and/or platelet clumps by fluorescent stain, and enhances the results accuracy and sensitivity. High automation to minimize the workload Throughput for 125 tests/hour, autoloader for 100 sample tubes capacity Bi-directional LIS with HL7 or ASTM communication protocol Customizable re-exam rules allow users to define their re-exam criterion according to lab’s practice

The advanced BC-6800Plus not only provides more reliable routine CBC plus 5-part DIFF results, but also has a higher throughput of up to 200 samples per hour. Based on the new SF Cube technology platform, the BC-6800Plus could provide more reliable blood cell results and abnormal cells flagging results with anticipated warning messages, exceeding clinicians’ expectations and setting a new standard for blood analysis. SF Cube Technology With the newly designed opticals and reagent systems, the SF Cube technology can help doctors to better differentiate the clusters of cells, which is the key to revealing more abnormal cells. NRBC result in every CBC In WNB scattergram, BC-6800Plus provides NRBC, Basophils and WBC-N* results. It means that the actual number of NRBCs can be measured in routine CBC, if they are present in the sample. Basophils are counted in this counting channel with NRBC results. Basophil and NRBC results are generated on BC-6800Plus without extra reagent or cost. NLR parameter in each CBC+DIFF Neutrophil-to-lymphocyte ratio (NLR) is calculated by dividing neutrophil count by lymphocyte count, usually from peripheral blood sample. In laboratory medicine, NLR is used as a marker of subclinical inflammation. According to clinical studies, NLR can be used as a prognostic factor of severe illness in COVID-19 patients. More accurate RET and PLT-O result By utilizing the new fluorescent dye, the reticulocytes and platelets are more specific stained with stronger fluorescent signal, that brings more reliable reticulocyte and platelet results. Automatic Rerun & Reflex Should the sample results trigger the criteria, the sample rack can automatically step back for a “rerun” or “reflex” check. 200 test/hour BC-6800Plus can load up to 100 samples at a time and offers a throughput of up to 200 tests per hour.

n large laboratories, rows of instruments are seen working tirelessly like miniature factories – only they produce not commodities but medical test results. Mindray CAL 8000 new-generation cellular automation line is one of them, but unlike a typical workhorse, it is intelligent. It is a highly automated workstation for smarter, faster, and more accurate cellular analysis. It can perform competently in the face of these challenges. The workstation can hold up to four units of BC-6800 automated hematology analyzer, which utilizes the advanced SF Cube technology and 3-D scatter grams to help doctors better differentiate blood cell populations and reveal abnormal cells undetectable by conventional techniques. With 125 CBC tests per hour per unit, BC-6800 brings the process rate of the workstation to 20–30 percent higher than other similar models, effectively alleviating laboratory's stress during the peak processing hours. On CAL 8000, the hematology analyzer, slide maker and stainer, CRP analyzer, and HbA1c analyzer are all integrated into one seamless production line through automated track modules and trolley. Simply by loading a single tube of blood sample onto the automation system, one can get all the test results. This innovative walk-away automation functionality has made possible the CBC+CRP+HbA1c testing all in one streamlined workstation for the first time in the industry. It offers a smart solution, or rather, a smart expert – the labX pert 2.0. It is a software that can automatically sort out the suspected samples for manual validation. The pathologist then decides if rerun or microscopic review is warranted based on their clinical experience. It avoids wasting slides and reduces extra work. Moreover, the onboard automated re-exam functionality also helps enhance work efficiency. The CMU software The touch screen is the “brain” of CAL 8000. It optimizes the distribution of workload between each analyzer unit and decides which sample requires a blood smear. It displays the status of each analyzer or SC-120 installed on CAL 8000 as well as the volume of balance reagent. This intuitive software can tell the users all necessary information of CAL 8000 at any given time. Consequently, the users spend less time operating CAL 8000 and can arrange their working schedule better. Multi “R” tests The CAL 8000 can automatically distribute the samples with “Repeat”, “Rerun” and “Reflex” criteria which are pre-defined by users.The re-exam criteria on CAL 8000 can be defined by many conditions, such as time, patient’s age, gender, department, etc. This helps minimize the number of blood smears. Special tube racks The special tube racks utilize different barcodes to differentiate specific testing purposes, such as “QC”, “Slide making & staining only” and “RET test only”. The special tube racks can carry the tubes to perform these specific functions in the simplest way.

Palm-sized, fitting easily into a doctor's bag or uniform pocket. The printer can be separated from the "PocketChem" analyzer, leaving it with a weight of just 180g. Corrective features for obtaining accurate test results Accurate readings can be obtained by eliminating the effects of chromaturia using the color correction test pad, by compensating measurements for the temperature of the surrounding environment using a built-in temperature sensor and by correcting specific gravity based on pH readings. Palm-sized analyzer driven by two batteries The analyzer is detachable from the printer. The analyzer is really portable and mobile. Simple operation. Just press the start button Measurement is performed by simply pressing the start button and placing a test strip. Test results can be simultaneously viewed on the display and printed out from the printer. Reliable test results with Creatinine correction Even with the use of spot urine, test results are reliable and are not affected by urine dilutions or concentrations. The P/C ration or A/C ratio is effective for the screening of renal diseases. Sample Urine Test strips AUTION Sticks/ Uriflet S (9UB)* / AUTION SCREEN * Except devices with 10V specifications Measurement items GLU (glucose), PRO (protein), BIL (bilirubin), URO (urobilinogen), S.G. (specific gravity), BLD (blood), PH (pH), KET (ketones), NIT (nitrite), LEU (leukocytes), CRE (creatinine) and ALB (albumin). Measurement principle Test strip: Dual wavelength reflectance method. (one wavelength for BLD measurement) Measurement wavelengths 3 wavelengths LED (565, 635, 760 nm) Sample supply method Manual dipping Measurement capacity 50 tests per hour Test strip reaction time About 60 seconds per test Measurement types Normal measurement and check measurement Display Custom LCD that displays information including type of test strip, measurement number (up to 4 digits), patient ID (up to 13 digits) and test results. Operator panel Panel sheet that provides 14 buttons including numeric buttons and start button. Memory capacity Test results for 100 samples External output Compliant with RS-232 C Measurement environment Temperature: 10 to 30 °C; Humidity: 30 to 60 % R.H. (non-condensing) *Temperature correction function used Dimensions 124 (W) x 81 (D) x 36 (H) mm Weight 180 g (without batteries) Power supply Instrument only: Two AA alkaline batteries or AC adapter Instrument with printer: AC adapter 7.5 V 3 A Power consumption 3 W Printer specifications Printer Thermal recording printer Printer paper High color development thermal paper (W 58 mm x φ26 mm) Dimensions 125 (W) x 133 (D) x 36 (H) mm Weight 180 g (without printer paper) Power supply AC adapter 7.5 V 3 A Power consumption 20 W

Autochem Ingeniious is a semi automated clinical chemistry analyser & has been designed to meet the demands of the research as well as laboratory staff. Compact ergonomic design which is ideal for use in small-to-medium-sized laboratory. In-built Peltier regulated incubation compartment Integrated Coagulation Testing Mode Single & profile wise testing facility Flexible calibration modes Direct access key to run tests Enhanced Patient Data Storage & Retrieval Daily & monthlty QC program Wash & Aspiration function can be controlled using External Keyboard (PS/2 keyboard) roduct Specification Automation Semi Automatic Brand ARKRAY Assays Clinical Chemistry Power Supply Input Voltage : 90-260 VAC, 50/60 Hz Reaction Cuvette Flow Cell Weight <10 kg Power 100 Watts Max Country of Origin Made in India

The Autochem Xact Pro is a Fully Automatic Random Access Clinical Chemistry Analyzer. It is a compact, benchtop analyser with throughput up to 200 tests per hour. First-in-Class On-board Warm-water Laundry System Probe with Collision-Protection System Multi function Probe which works as mixer also Probe with Capacitance based liquid level sensor Robust Multi-functional Software Intelligent" Mixing Arm Removable & flexible Sample - Reagent Disc with 40 Open position for reagent & samples respectively. DESIGNED FOR UNINTERRUPTED WORK FLOW OTHER FEATURES ROBUST MULTI-FUNCTIONAL SOFTWARE Probe with Collision-Protection System Both horizontal and vertical collision protection ensures that system re-starts testing after any unwanted physical intervention. This prevents wastage of reagents, saves test time and increases life of probe Multi functional Probe Probe has flexibility to work even as a mixer in case in-built mixer does not work Probe with Capacitance based liquid level sensor Probe with liquid level sensor checks and indicates the presence of adequate sample or reagent in the container before starting testing process. Thus prevents unwanted interruptions in testing process “Intelligent” Mixing Arm User defined, variable three level mixing speed ensure thorough mixing Accurate performance of regular and immunoturbidimetric assays Independent cleaning station for mixer which prevents carry-over ensuring high precision Removable & flexible Sample – Reagent Disc 40 Open position for reagent & samples respectively Facility to use primary & variable sample cup as well as non fixed position for Sample, Control, Calibrator & STAT samples Two bottle sizes of 18 mL or 5 mL with unique design to reduce reagent dead volume Optional internal Reagent & Sample barcode reader makes the operation user friendly & ensure correct result reporting Reaction tray 60 reusable plastic reaction cuvettes which is also scanned before performing the test which means less recurring cost without compromising on quality. To assure precise results Individual replacement of cuvette offer lower consumable cost REFLEX Testing Functionality Allows user to program Low & High panic value for a particular test which triggers auto-testing of assigned tests which ensures faster and comprehensive reporting Dynamic & Real-time display of Test Running Status for quicker decision making Running status of reagent tray, Sample tray & reaction tray Real-time monitoring of Reaction curve On board inventory management Real-time monitoring of reagent residual volume saves reagent cost & time In-built full QC Program Provision to run 3 levels of control with Levey Jennings graph which gives confidence in reporting with multiple rules (1SD, 2SD and 3SD) Reagent, Calibrator & Control lot monitoring User friendly Bi-Directional LIS Interface

STANDARD GlucoNavii Pro BT It can measure blood glucose through venous, capillary, arterial blood and as well as neonatal blood using GDH-FAD enzyme.. Its Easy Light™ function helps the user check the glucose level through the LED light and the ejector allows an easier removal of the strip. By using Bluetooth(BLE), it helps manage blood glucose levels through smart devices. Advantage Blood glucose data transfer using NFC and Blootooth(BLE) communication technology GDH-FAD enzyme (Capillary, Venous, Arterial and Neonatal blood available) No Coding Fasting, Pre & Post Meal Mark Wide Hematocrit Range(0~70%) Strip Ejection Function Easy Light™(Glucose level indicaitor) Specification Enzyme Glucose Dehydregenase-FAD biosensor Measurement Range 10 - 600mg/dL (0.6 - 33.3 mmol/L) Test Time 5 sec Sample Volume 0.5 µl Hematocrit 0 - 70% Unit mg/dL Memory Up to 1,000 tests Battery 3V battery (CR2032) Interpretation of results Cat. No. Product Component Note 01GC610 STANDARD™ GlucoNavii® PRO Blood Glucose Monitoring System Meter, Meter, Test Strip (10EA) / Lancet(10EA) / Lancing Device 01GS60 STANDARD™ GlucoNavii® PRO Blood Glucose Test Strip STANDARD™ GlucoNavii® PRO Test Strip (25EA x 2 bottle) Download