The SAL 9000 Modular System delivers high throughput of chemistry and immunoassay testing by integrating Mindray BS-2000 Chemistry Analyzer and CL-6000i Chemiluminescence Immunoassay Analyzer, and new Sample Processing line SPL 2000. With patented automatic serum analysis design, SAL 9000 not only helps you optimize the management of lab space and manpower, it also offers highly reliable test results. Product Specification Automation Fully Automatic Brand Mindray Model Name/Number SAL 9000 Assays Clinical Chemistry Power Supply 230 V Reaction Cuvette Reusable Cuvette Storage 300000 Samples Features Seamless Integration Usage/Application Lab Wavelength 5000nm Number Of Reagent Positions 4 Weight 130kg Frequency 50 Hertz Power 45 Watt Product Description The SAL 9000 Modular System delivers high throughput of chemistry and immunoassay testing by integrating Mindray BS-2000 Chemistry Analyzer and CL-6000i Chemiluminescence Immunoassay Analyzer, and new Sample Processing line SPL 2000. With patented automatic serum analysis design, SAL 9000 not only helps you optimize the management of lab space and manpower, it also offers highly reliable test results. Features Maximize laboratory efficiency Integration: Optimize your lab’s customized arrangement with better automation system Efficiency: High-throughput chemistry and immunology modules for longer walk-away time Reliability: Ingenious and comprehensive analytic system provides reliable and accurate results Easy operation: Fully automated design,user-friendly operation interface and intelligent software function

INTENDED USE The Finecare™ Estradiol (E2) Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters is for quantitative measurement of Estradiol (E2) in human whole blood, serum or plasma. The test is used as an aid to the evaluation of ovarian diseases. STORAGE AND STABILITY 1. Store the test kit at 4～30℃ up to the expiration date. 2. If removed from refrigerator, allow the test for 30 minutes to return to room temperature before testing. 3. Do not remove the cassette from the pouch until ready to use. The Test cassette should be used within 1 hour once opened.

INTENDED USE The Finecare™ β2-MG Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of β2-MG (Beta-2-Microglobulin) concentration in human plasma, serum or whole blood. The test is used as an aid for the diagnosis of renal disease. 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™ Lp-PLA2 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Lp-PLA2 in human serum, plasma or whole blood. The test is used as an aid to the assessment of the coronary heart disease (CHD) and ischemic stroke. 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™ 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.

Semiautomatic Clinical Chemistry & Turbidimetry Analyzer completely managed by microprocessors and equipped with a wide graphic display, 10 position thermostat programmable from 20°C to 40°C. The 3000 Evolution stores up to 120 different test programmers which can be easily programmed. Stable optics and automatic filter selection assures reliable and repeatable measurements. Calculations are performed automatically so that results are displayed or printed out directly in the required measuring unit.

SV300 Pro is dedicated to simplifying the use of ventilator. With the design in line with clinical needs, SV300 Pro is able to improve the efficiency of clinical operations and maintenances. Frameless Capacitive Screen Frameless designed capacitive screen, more precise touch and easier to clean and disinfect. Comprehensive Comprehensive With comprehensive ventilation modes and decision-supporting tools like SBT, the SV300 Pro manages to fit for the most stringent ICU environment. Intelligent Ventilation Adaptive minute ventilation(AMV TM ) together with IntelliCycle TM enables the ventilator to automatically adjust ventilator settings to reduce the need of frequent ventilator settings adjustment and improve the patient-ventilator synchrony. p69-s3-1 CPRV Ventilation CPRV TM is specially developed for CPR procedure. Quickly access the mode with one-click start, allowing precision ventilation and CO2 monitoring. When used with Mindray unique Electronic Impendence Threshold Device(e-ITD TM ) technology, it can further improve the efficacy of CPR with increase venous return and perfusion. p69-s3-2 Adaptive With a weight no more than 10kg, equipped with powerful turbine and integrated CO₂/SpO₂ monitoring, the SV300 Pro is appropriate for all levels of patient acuity and in all care settings, from the patient's bedside to another point of care with its intra-hospital transport friendly designs.

The SV300 is a state-of-the-art ventilator that's simple to configure, easy to operate, and versatile in use. It treats pediatric and adult patients with all acuity levels at ICUs and Intermediate Care. Adaptive With its comprehensive list of standard features, including the latest modes of ventilation, the SV300 is appropriate for all levels of patient acuity and in all care settings, from the patient's bedside to transport to another point of care. Comprehensive Equipped with functions that are usually found on intensive care ventilators, the SV300 comes with extensive ventilation modes and unique features that make it a top level ventilator. p84-s4-1 Volumetric CO₂ measurement p84-s4-2 Weaning indicators p84-s4-3 O₂ Therapy p84-s4-4 Intelli Cycle Thanks to the intuitive UI design of the SV300, each function is in logical order so that clinicians do not need to navigate a complex menu. In addition, both the valves and flow sensor support autoclaving. This safety concept is designed to meet the current clinical trends of protecting patients even under the most demanding conditions.