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.

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

A high-end ventilator featured with 1080P HD wide screen, combines an intuitive customized UI with powerful assistive tools and modules. 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 SV800/SV600 ventilators enable clinicians to set and deliver ventilation therapies quickly and easily via the intelligent ergonomic design and flat user interface. Intelligent Decision Making Ventilation modes and decision-supporting tools like SBT are developed on the basis of clinical needs and professional guidelines to help free up medical personnel’s time on device operation and focus more on their patients. p68-s4 Extensive ventilation therapy and decision support tools Smart ventilation solution: AMV TM + IntelliCycle TM Emergency solution: CPRV TM 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 features and technologies. The SV800/SV600 ventilators allow just this. Thanks to latest software and platform it is utilizing, your device is ready to embrace new technological advancement with ease. p68-s0-0 Integrated neonatal module with tidal volume setting down to 2ml Plug & Play modules , including SpO₂, mainstream or sidestream CO₂ Backup air supply in case of central air supply failure and during intra-hospital transport Seamlessly connected to the hospitals clinical information system via the Mindray BeneLink and eGateway modules, or directly via the HL7 p68-s5 Brand - Mindray Model Name/Number SV800 Patient Age Group Adult, Pediatrics & Neonatal Tidal Volume For adult : 100 to 4000 ml, For Pediatric 20 to 300 ml, For neonatal : 2 to 100 ml Ventilation Mode V-A/C, P-A/C, V-SIMV,P-SIMV, Duolevel, CPAP, PSV, APRV, PRVC, NIV, PRVC-SIMV, AMV, CPRV, PSV-S/T, nCPAP, VS Respiratory Rate For adult/pediactrics : 1 to 100/min,for neonate :-1 to 150/min Additional Details Weight 45 kg ventilator + 16.3 kg trolley Plateu (%) OFF, 5% to 60% Peak airway pressure 0 to 100 cm H2O SIMV Rate ,Cycle/min 1 to 60 rpm Mounting type Trolley I:E Ratio 1:10 to 4:1 Touch screen 18.5 inch color active matrix TFT touch screen RSBI 0-9999/1/(L-min) Features Customizing the UI Graphic guidelines Single level menu design Dual channel auxiliary pressure monitore

The Resona I9, a general imaging ultrasound system with completely innovative features from inside out. All innovations are developed based on in-depth insights into complex clinical scenarios, providing accurate and timely answers as well as outstanding efficiency and a remarkable user experience. Unlimited Scanning Flexibility Beyond Imagination iConsole - Intelligent Control Panel • Intelligent and clinical exam-specific control panel layout with special E-ink keys • Breakthrough design with adaptive layout for different clinical scenarios Full-space Floating Control Panel Can be adjusted for better space utilization, Easily meet various scanning needs Thoughtful Design for Ultimate Convenience 23.8" bezel-less full-screen with large images for immersive experience Eye-protecting monitor with adaptive brightness adjustment 15.6" full-HD touch screen with intuitive interaction Short-cut switch of latest used probes and exams Bring Optimal Patient Care Immediately Just Fold Down and Go Minimum 1 meter height Easy transportation by MPV (Multi-Purpose Vehicle) for mobile service Bedside Exams Without Power Cables • Up to 4 hours continuous scanning • Auto indication of residual power when you grasp the right handle

Accu-Chek® Active blood glucose meter Personalised Diabetes Coaching Accurate, no coding, easy Item Description The Accu-Chek Active blood glucose meter packs many powerful features into a smaller size. No coding reduces handling steps, see test result averages up to 90 days, get alerts if your test strips are expired or if you’ve underdosed, re-dose within 10 seconds, set pre-and post-meal reminders to test, and more. Benefits and Features accurate: Accurate1 blood glucose measurement easy: No coding for even easier blood glucose monitoring easy-to-read display (new typeface) intuitive handling with just 2 buttons safe: Underdose detection visual double check 10 seconds re-dose option clever: Pre- and postmeal markers postprandial reminder 7,14,30 or now 90 day test averages USB interface for data transfer Remark: Previous Accu-Chek Active meter generations will be upgraded to no coding via black activation chip . Know more>> 1The Accu-Chek Active bGM system meets the DIN EN ISO 15197:2013 requirements (data on file, 2014). Additional specifications Meter type : Accu-Chek Active meter (Model GB) Catalogue no. / Serial no. : See type plate on the back of the meter Test principle : Determination of glucose in fresh capillary blood by reflectance photometry. Blood glucose values can be tested in whole blood or plasma. The meter displays blood glucose values corresponding to those in plasma. Measuring interval : 10-600 mg/dL Blood volume : 1-2 μl Measuring time : Test strip in the meter: approx. 5 seconds Test strip outside the meter: approx. 08 seconds Power supply : 1 battery (type CR2032) Battery life : approx. 1000 tests or approx. 1 year Automatic power-off : after 30 or 90 seconds depending on operating status Memory : 500 test results with time and date, as well as 7, 14, 30 and 90 days averages Temperature : During testing: +8 to +42°C During storage without battery: -25 to +70°C During storage with battery: -20 to +50°C Atmospheric humidity : During testing: up to 85% relative humidity During testing: up to 93% relative humidity Altitude: Sea level to 4000 m Dimensions : 97.8 x 46.8 x 19.1 mm Weight : Without battery: approx. 46 g With battery: approx. 50 g Display : 96-segment liquid crystal display (LCD) Interface : USB (Micro B) Safety class : III Electromagnetic compatibility : The Accu-Chek Active meter meets the electromagnetic immunity requirements and the electromagnetic emissions requirements as per EN 61326-2-6 and EN ISO 15197 Annex A. The chosen basis for electrostatic discharge immunity testing was basic standard IEC 61000-4-2. Performance analysis : Calibration and traceability: The performance data for the Accu-Chek Active bGM system was calibrated using venous blood containing various glucose concentrations. Reference values are obtained using the hexokinase method, which is calibrated using the ID-GCMS method. Accuracy performance : The Accu-Chek Active bGM system meets the DIN EN ISO 15197:2013 requirements (data on file, 2014). How to use Accu-Chek Active blood glucose meter Testing your blood glucose is an essential part of managing diabetes. The Accu-Chek Active blood glucose meter can help to make it convenient by giving you fast, hassle-free, and accurate results in 4 simple steps. Insert the glucose test strip Prick your finger with the lancet to draw out a blood drop. Carefully touch the blood drop onto the green field of the test strip. Read the blood glucose result.

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.