STANDARD E TB-Feron ELISA This product is a blood assay that can help to diagnose human tuberculosis using IGRA (Interferon Gamma Releasing Assay) method. Advantage Sensitive and specific IGRA test Unlike the classic way of tuberculin test (TST), TB-Feron ELISA only needs one clinic visit Not affected by Bacille-Calmette Guerin (BCG) vaccinations

HumaScope ClassicLED is Particularly suitable for remote health care settings: Rechargeable battery allows for independence from constant power supply up to 5 days LED illumination: no replacement bulbs required Objective - Semi-Plan achromatic 4x, 10x, 40x, 100x (oil Immersion) Head – Binocular, Compensation Free Eyepiece – Widefield, 10x /18mm, Diopter Adjustment Revolver – Five Positions Reverse These are microscopes for education and routine laboratory applications; they are high-performing, durable imaging systems at affordable prices. They have robust mechanical construction combined with brilliant optics and latest LED technology as well as battery operation mode, making them first choice for health care settings especially in remote areas.

A Truly Automated Walkaway ESR Analyzer for Midsize labs (Meets CLSI and ICSH Guidelines) Product Features: Gold Standard Method -Measures all three phases of sedimentation as per Westergren method Dry Technology - No sample & reagent consumption, no waste generation Faster TAT - Throughput of 60 samples/hr Zero consumption cost by using EDTA tubes HCT correction feature eliminates manual correction in Anaemic samples Temperature correction at 18° ensures reliable results No additional cost of Calibration Analyzer Product Code Product Name Pack size ESL 30 122020 SMART CARD 2500 1x 2500 ESL 30 122021 SMART CARD 5000 1x 5000 ype of Sample : EDTA Sample Volume : > 1.5 ml Display : TFT high resolution 640 * 480 dots with LED Backlight Result Cycle Time : < 25 min Measuring Range : 0-140 mm/hr Touch screen : 5.7 inch resistive TFT high resolution Temperature Correction : At 18 Degree HCT Correction : HCT Correction facility available for Anaemic samples QC : Inbuilt Quality Control program with LJ Graphs Quality Control Level : 3 Level QC with LJ Graph QC Data Storage : 250 QC results Sample position : 30 sample position Throughput : 60 samples per hour Sample Consumption : No Type of Mode : Continuous mode STAT Facility : Available Calibration Requirement : No Mixer : Inbuilt Mixer Printer : Inbuilt Printer Barcode reader : Inbuilt Barcode reader Data Storage : 5000 results Operating Temperature : 20 - 30 Degree Celsius Storage Temperature : 15 - 35 Degree Celsius Relative Humidity : Max. 80% RH Power Adapter external : 240V DC , 90W Main supply : 100V-240V AC, 50/60 Hz (input for power adapter ) Dimension (mm) : 550(L) x 500 (W) x 395 (H) Weight : 20 kg (Approx )

INTENDED USE The Finecare™ One Step cTn I/CK-MB/Myo Rapid Quantitative Test a fluorescence immunoassay to be used along with Finecare™ FIA System for quantitative determination of cardiac Troponin I (cTn I), MB Isoenzyme of Creatine Kinase (CK-MB) and Myoglobin (Myo) in human whole blood, serum or plasma. The test is used as an aid to the diagnosis of myocardial infarction. STORAGE AND STABILITY 1. Store Finecare™ One Step cTn I/CK-MB/Myo Rapid Quantitative Test at 4 ℃~30 ℃. Do not freeze. Shelf life is up to 24 months, refer to label for expiration date 2. If removed from refrigeration, allow the Test Cartridge for 30 minutes to reach room temperature (25±2℃) before testing. 3. Once opened, commence to use the Test Cartridge within an hour. 4. Do not remove the device from the pouch until ready to use. Keep the Test Cartridges away from light.

INTENDED USE The Finecare™ 2019-nCoV RBD Antibody Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for qualitative and semi-quantitative detection of spike receptor-binding domain (RBD) antibodies of novel coronaviruses (2019-nCoV) in human fingerstick whole blood, venipuncture whole blood, serum or plasma specimen. The 2019-nCoV RBD antibodies are protective antibody produced by the human body after inoculation with 2019-nCoV vaccine or infection with 2019-nCoV. The test is intended as an aid to assess the adaptive humoral immune response to the 2019-nCoV RBD protein. STORAGE AND STABILITY 1. Store at 4~30°C in the sealed pouch up to the expiration date printed on the package. Do not freeze. 2. The test device should be used within 1 hour after taking out from the foil envelope. 3. Keep away from sunlight, moisture and heat. 4. Kit contents are stable until the expiration date printed on the outer box.

INTENDED USE The Finecare™ 2019-nCoV lgM/lgG Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for qualitative detection of IgG and IgM antibodies of novel coronaviruses (2019-nCoV) in human whole blood, serum and plasma specimen. Clinically, the test is to be used as an aid in the diagnosis of coronavirus infection disease (COVID-19), which is caused by 2019-nCoV. The test provides preliminary test results. Negative results cannot exclude the possibility of 2019-nCoV infection and they cannot be used as the sole basis for treatment or other management decision. STORAGE AND STABILITY 1. Store at 4-30°C in the sealed pouch up to the expiration date printed on the package. Do not freeze. 2. The test device should be used within 1 hour after taking out from the foil envelope. 3. Keep away from sunlight, moisture and heat. 4. Kit contents are stable until the expiration date printed on the outer box.

ADVIA 2400 Chemistry System The right balance of speed and efficiency The ADVIA® 2400 Clinical Chemistry System manages the most demanding workloads and meets high turnaround-time (TAT) goals. Its menu includes methods for testing drugs-of-abuse, therapeutic drugs (TDM) and new assays such as cystatin C and CardioPhase® hsCRP. The ADVIA 2400 Clinical Chemistry System offers: High throughput of up to 2400 tests/hour (1800 photometric and 600 ISE) to manage heavy workloads Rapid, consistent, 2-second cycle time for faster tube speed and test throughput User-defined automatic repeat, dilution, and reflex testing Large onboard reagent capacity and optional concentrated reagents help to minimize intervention demands Refrigerated onboard storage of controls and reagents for extended stability and increased productivity Automation-ready design: no additional hardware required Features & Benefits The ADVIA 2400 Clinical Chemistry System meets today’s high turnaround-time goals with a throughput of up to 2400 tests/hour. In addition to assays for general and specialty chemistries, its menu includes assays for specific protein measurement, drugs-of-abuse testing (DAT), and therapeutic drug monitoring (TDM). Interesting new assays such as cystatin C, HbA1c with automated sample pretreatment, and CardioPhase® hsCRP can now be included in your routine testing. The ADVIA 2400 Chemistry System pushes productivity levels while maintaining the reliability and stability that keep laboratories up and running. A rapid, 2-second probe cycle time maximizes tube speed and test throughput and combines with the system’s efficient automation-readiness to provide the turnaround time needed for high-volume laboratories Superior Speed and Productivity Throughput of up to 2400 tests/hour (1800 photometric and 600 ISE) to manage the heaviest workloads Rapid, consistent, 2-second cycle time Throughput of 200 tubes per hour, even when running three ISE tests and nine photometric tests per sample Automatic Sample Retain technology, auto-repeat, auto-dilution, and auto-reflex testing Automation-ready Point-in-space aspiration enables connectivity to a track. Redundant sample loading provides built-in backup and easy handling of non-routine samples. Direct sampling from track prevents tubes being detained at an analyzer and reduces aliquoting. Minimal Need for Operator Intervention Minimal-maintenance ISEs Large onboard reagent capacity and optional concentrated reagents for fewer interruptions No-maintenance, 37°C incubation oil bath Auto-calibration and auto-QC from refrigerated onboard calibrators and controls Microvolume technology with 32,000 tests onboard and up to 60 days' onboard stability for improved walkaway time. Concentrated reagents for increased maximum capacity. Remote diagnostics and Inter-Laboratory Quality Control (ILQC) options Exceptional Reliability Sample integrity check for icterus, hemolysis, and lipemia Sample probe with automatic clot/clog detection, liquid-level sensing, short-sample detection, and crash protection Advances in onboard reagent stability, calibration frequency, reduction in interferences, and expanded assay linearity

ADVIA Chemistry XPT System An advanced, automated clinical chemistry analyzer for high-volume laboratories The ADVIA® Chemistry XPT System provides timely, reliable results with continuous operation to meet the chemistry workloads of the most demanding laboratories. Delivers high throughput of up to 2400 tests per hour. Manages comprehensive testing with a menu of more than 115 assays. Improves workflow using automation and system technologies such as micro-volume and aliquot retention. Features & Benefits The ADVIA Chemistry XPT System*** is engineered for continuous operation and timely, accurate results—supporting you to reach your full potential today and be prepared for tomorrow. With an advanced user interface that is easy to use and VeriSmart Technology to support accuracy of testing, the ADVIA Chemistry XPT System predictably and consistently delivers timely, reliable results to meet expanding workloads. Simplified, Continuous Operation Simplify operation and training with the intuitive, icon-driven user interface. Extend walkaway times with concentrated reagents that provide high test capacity onboard. Quickly load most system fluids on the fly. Automate calibration, QC, startup, and shutdown. Consistent, Predictable Turnaround Time and Accuracy Offer a comprehensive chemistry menu of over 115 assays, including general and specialty chemistry, DAT, TDM, and specific proteins. Push productivity with a throughput of up to 2400 tests per hour (1800 photometric, plus 600 ISE). Control testing: STAT and specialty samples can always be front-loaded while an automation track is running. Designed for Automation Adapt and grow with direct connectivity to Siemens Healthineers and . Simplify your laboratory operations with connectivity to IT solutions including , , and . Increase productivity and efficiency with direct-from-track sampling and onboard aliquoting that allows samples to be immediately released to the next workstation. Do More with Less Reduce blood-draw requirements with micro-volume technology that uses a single 30 μL sample for up to 15 tests. Eliminate sample callback with automated, pre-programmable dilution, reflex, and rerun testing that uses an onboard aliquot. Improve workflow and accuracy with VeriSmart echnologies that perform hardware and software checks at all stages of sample processing.

HyPort B30 With the higher requirement of the healthcare, and continuing focus on the efficient clinical workflow, the advanced medical technology is always demanded from the patients and hospital. While some hospitals have limited space and budget, they search for a simple pendant solution to enhance the work efficiency and better care for the patient. Mindray HyPort B30 provides a simple, compact and cost-effective design for Anesthesia Pendant and Surgical Pendant in OR and ICU Pendant to meet this requirement. Less space needed with slimmer column design Easy to handle for nurse after reducing pendant weight Hygienic surface with anti-bacteria coating Built-in rails for accessories and no exposed screws