Designed to fulfill the clinical requirements of minimally invasive surgeries, Mindray's HD3 endoscope camera system comes with the advanced 3-chip CMOS sensor, premium optical lens, real-time optimization software and a FHD screen. Through delivering exceptional image quality and user experiences, the HD3 endoscope camera system enables surgeons to focus on their patients, helping facilitate more accurate diagnosis and treatments. HD3 Camera System 3-chip CMOS sensor FHD picture taking and video recording with USB port Advanced parfocal technology 2X optical zoom Focal length: 14mm-30mm Laparoscopes · High-resolution images and outstanding color rendition · Scratch-resistant sapphire lens · Fog reduction function · Autoclavable lens · Compatible with third-party optical fiber cables HS50 Insufflator · Maximum flow rate: 50L/min · Large 7-inch touchscreen · Gas heating function · Smoke evacuation · Automatic flow compensation · Auto-switchover between veress needle mode and trocar mode · Up to 5 insufflation modes, satisfy all insufflation needs HB200L LED Light Source · Equivalent to 300W Xenon light source · Autoclavable light cable · Auto-detection of light guide cable · Light intensity indicator · LED life expectancy: 40,000 hours PV27 FHD Monitor · 1920*1080 resolution · Picture-in-picture mode · Adjustable brightness · Flexible input: DVI,SDI,S-video,VGA

For smaller Laboratories Smaller, but with full functionality Compact size Full functions and performance in a compact size. *Size comparison with HA-8180V Accuracy HPLC technology provides accurate results-inluding detailed chromatogram. it will be shown in both IFCC and NGSP units. Cap-piercing method ADAMS Lite uses a cap-piercing method which enables the placement of capped blood samples. This not only reduces the workload but also helps protect lab technicians from infection. Easy-to-maintain No special tools are required for daily maintenance. Exchanged parts are hand-tightened, minimizing the workload of users. Specifications Measurement objects Whole blood or hemolysis sample Measured items Fast Mode: HbA1c (Stable HbA1c, S-A1c) and HbF Variant Mode: HbA1c (Stable HbA1c, S-A1c) and HbF (HbS and HbC separation and HbE and HbD detection can be performed). Measurement principle Reversed-phase cation exchange chromatography Measurement wavelength 420 nm/500 nm (Dual-wavelength colorimetry) Resolution 0.1% Ratio, 1 mmol/mol Measurement range HbA1c: 3 - 20%, 9 - 195 mmol/mol HbF: 0 - 100% Processing speed Variant mode: 160 seconds/test Fast mode: 100 seconds/test Sample consumption Whole blood sample: Approximately 4µL Anemia sample: Approximately 8 µL Hemolysis sample: Approximately 350 µL Sample container Sample tube: (12.3 or 15 mm in outer diameter) × (75 to 100 mm in height) Sample cup: 500 µL Sample supply Piercing sampling Compatible rack type ARKRAY racks (for 5 samples) Operating environment Temperature: 10 - 30°C; Humidity: 20 - 80% RH (No condensation) Display 20 digits × 2 lines LCD Printer For use with 58-mm width thermal printer paper Number of measurement samples Maximum 10 samples Power requirements AC 100 - 240 V±10%, 50/60 Hz Dimensions 330 (W) × 515 (D) × 485 (H) mm (Not including protrusions, eluent packs and hemolysis washing solution bottle)

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.

Beurer BM 29 upper arm blood pressure monitor The universal cuff means the device is also suitable for larger upper arm circumferences. One for all the blood pressure monitor has a universal cuff that is also suitable for larger upper arm circumferences up to 42 cm. The integrated cuff position control gives you additional certainty about the accuracy of the measured blood pressure values during each measurement. Universal cuff, including for larger upper arm circumferences up to 42 cm Fully automatic blood pressure and pulse measurement on the upper arm Average of all saved measured values Cuff position control 2 adjustable alarm times Easy-to-read display 4 x 30 memory spaces Risk indicator Arrhythmia detection Medical device For upper arm circumferences from 22 to 42 cm Date and time/automatic switch-off Incorrect usage message Low battery Indicator No Storage box available.

Oscar Corona IgG Antibody Detection Test is a rapid test based upon lateral flow immunochromatography principle for the qualitative detection of IgG antibodies against Novel Corona Virus (COVID-19) in human serum, plasma or whole blood. For professional and in-vitro diagnostic use only.

Oscar Corona Antibody Detection Test is a rapid test based upon lateral flow immunochromatography principle for the qualitative detection of antibodies against Novel Corona Virus (COVID-19) in human serum, plasma or whole blood. For professional and in-vitro diagnostic use only. Sensitivity: 97.66% Specificity: 99% Pack Size: 25 Tests

Product Description: Erba Lisa Wash II is a simple easy to Operate and use ELISA Plate Washer, Suitable for all ELISA applications. Programmable features like, dispense pressure, Single/double aspiration, Horizontal & Vertical adjustments ensures complete control on washing efficiency Product Features: Fully automated, easy operating system and friendly software with large-screen display 50 user programmable protocols to customize washing Easily removable 8- or 12-way manifolds Liquid level detection and alert function Low residual volume: <3 µl Soak time programmable up to 24 hrs. Compatible for flat-bottom, U and V bottom type microplates or microstrip High-efficiency ELISA washing with automated monitoring of Vacuum. Choice of 2 wash buffer bottles, 1 distilled water & 1 waste container with sensor Dispense pressure and the volume adjustable, so as to reduce the air bubbles and ensure thorough Washing Waste-bottle sensor to detect high-waste liquid levels Standard aerosol protection cover Easy maintenance CE marked Product Applications: ELISA Wash Head: 8 and 12 head manifold compatible Wash Mode: Row and Plate Wash Row: 1-12 rows Flat Bottom Plate Type: 96 or 48 well plate or strip (Flat, U & V - bottom) Wash Programs: 50 Moving Cycle: up to 12 cycles Dispensing Volume: 50 - 3000μl in 50μl increments Dispensing Precision: < 2% at 350μl Prime Volume: 50 - 1000μl Aspiration Pressure: Automatic Soak Time: 0 – 24 Hrs Residual Volume: ≤ 2μl for V/ U bottom plates, and ≤ 3μl for per well Flat bottom plates Nos. of Bottles: 2 wash, 1 Rinse/DI, 1 waste with level sensor, 2L each User Interface: 5 Inch LCD (90 x 53 mm), with Keypad Bottle Capacity: > 2 L Operating Environment Power Supply: AC 220 V/ 110 V, 50/60 Hz Input Power : < 80VA Operating Temperature: 10°C - 30°C Relative Humidity: Up to 95% relative humidity without condensation Storage Temperature: -10°C - 40°C Weight: 9.5 Kg Dimension: 710 mm x 530 mm x 380 mm

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.