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

Buy AccuTest COVID-19 IgG/IgM Rapid Test (Pack of 10 Tests) Online. COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. Intended Use: COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. SUMMARY & TEST DESCRIPTION: COVID-19 [Coronavirus Disease- 2019] is an infectious disease caused by SARS-CoV2 [Severe Acute Respiratory Syndrome coronavirus 2] virus, which is a contagious, novel strain of CoronaVirus that emerged from Wuhan, China in December 2019, which grew as a pandemic threatening human survival across the globe. The virus is thought to be of zoonotic origin and likely to have spread from large seafood and animal markets by human-animal contact in the city of Wuhan, where consumption of such products is in large. The virus causes respiratory infection with symptoms including fatigue, fever, shortness of breath, respiratory failure, renal failure and death. Patients can become infected with SARS-CoV-2 virus by person-person contact (through contact with a contaminated environment or person). The young and old (and other immune-compromised individuals) are most at risk of serious complications; however, approximately 20% of those infected can develop a critical condition. COVID-19 IgG/IgM Rapid Test device utilizes Anti-human IgG and Anti-human IgM antibodies as the capture molecules. COVID-19 Recombinant Antigens-colloidal gold conjugate are used as detection antigen. Intended Use: COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. SUMMARY & TEST DESCRIPTION: COVID-19 [Coronavirus Disease- 2019] is an infectious disease caused by SARS-CoV2 [Severe Acute Respiratory Syndrome coronavirus 2] virus, which is a contagious, novel strain of CoronaVirus that emerged from Wuhan, China in December 2019, which grew as a pandemic threatening human survival across the globe. The virus is thought to be of zoonotic origin and likely to have spread from large seafood and animal markets by human-animal contact in the city of Wuhan, where consumption of such products is in large. The virus causes respiratory infection with symptoms including fatigue, fever, shortness of breath, respiratory failure, renal failure and death. Patients can become infected with SARS-CoV-2 virus by person-person contact (through contact with a contaminated environment or person). The young and old (and other immune-compromised individuals) are most at risk of serious complications; however, approximately 20% of those infected can develop a critical condition. COVID-19 IgG/IgM Rapid Test device utilizes Anti-human IgG and Anti-human IgM antibodies as the capture molecules. COVID-19 Recombinant Antigens-colloidal gold conjugate are used as detection antigen. PRECAUTIONS & WARNING 1. This package insert must be read completely before performing thetest. Failuretofollow directions in insert may yield inaccurate test results. 2. Test results should be read between 10 and 15 minutes after aspecimenisapplied to the sample well. Results read after 20 minutes may giveerroneousresults.3. Do not open the sealed pouch until you are ready to conduct theassay.Onceopened, the cassettes should be used immediately. 4. Do not use expired devices. 5. Bring all reagents to room temperature (15-30°C) prior to use. 6. Do not mix components from different kits. Use only the buffer suppliedalongwith the kit. 7. Wear protective clothing and disposable gloves while handling thekit reagentsand clinical specimens. Wash hands thoroughly after performing thetest. 8. Do not smoke, drink, or eat in areas where specimens or kit reagents arebeinghandled. 9. Dispose of all specimens and materials used to performthe test as biohazardouswaste. 10. Handle the negative and positive controls in the same manner as patientspecimens for operator protection. 11. Do not perform the test in a room with strong air flow, i.e. an electricfanorstrong air-conditioning. 12. Do not touch result window. 13. Use only for in-vitro diagnostic purpose.

INTENDED USE The Finecare™ LH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Luteinizing hormone (LH) in human whole blood, serum or plasma. This test is used as an aid to diagnose the ovulation cycle, premature ovarian failure and gonadal hypoplasia. 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™ BNP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Brain Natriuretic Peptides (BNP) in human whole blood or plasma. This test is used as an aid to predict the risk of heart failure. 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™ cTn I/NT-proBNP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of cardiac Troponin I (cTn I) and N-terminal prohormone of brain natriuretic peptide (NT-proBNP) in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of myocardial infarction and suspected congestive heart failure. 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.

Getein 1200 Immunofluorescence Quantitative Analyzer Truly automated, truly modular, truly intelligent and truly dry system. The instrument has low failure rate and moderate measurement speed, which is convenient for clinical departments with medium and high throughput use.

The NB350 neonatal noninvasive ventilator is specially designed for neonatal ventilation, equipped with comprehensive NIV modes to provide reliable non-invasive respiratory support to meet the various needs of neonatal respiratory management. EasySync™ Technology The patented EasySync™ technology analyzes multi-channel parameters including gas flow and pressure without additional sensors, enabling accurate detection of spontaneous breath and improving synchrony in SNIPPV. The EasySync™ technology leads to a good synchronization performance comparable to electrical activity of the diaphragm (Edi). IOC (Intelligent Oxygen Control) The oxygen saturation of neonates tends to fluctuate, requiring caregivers to frequently adjust ventilator’s FiO2 settings. IOC (Intelligent Oxygen Control) achieves a closed-loop FiO2-SpO2 control by maintaining the patient’s SpO2 within the predetermined range, which reduces the workload of caregivers and improves patient safety. Integrated SpO2 monitoring for neonates in real time.1 Automatically adjust FiO2 setting by adaptive algorithm.2 Steadily maintain the SpO2 of neonates within the preset target range. Comfortable and Reliable Patient-interface The specialized patient-interface for the NB350 comes with a variety of sizes to fit for different clinical applications and patients. The ergonomic design with soft, skin-friendly material fully enhances the comfort of neonates throughout therapies. Bonnet/Headgear The bonnet/headgear integrate a fixings lot (seat) for pressure generator to avoid misposition and disconnection of patient-interface. Skin-friendly and breathable bonnet/headgear. Durable headgear hook-and-loop fastener allows easy and quick re-adjustment of the patient-interface. Infant Jet™ Pressure Generator Adjustable nasal prong/nasal mask positioning to adapt different facial orientations. Specifically designed to facilitate Coanda effect, significantly reducing respiratory resistance. Related Articles

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

The OnSite RSV Ag Rapid Test is a lateral flow immunoassay for the qualitative detection of Respiratory Syncytial Virus (RSV) antigens in nasopharyngeal swab or nasal aspirate specimens. No cross-reactivity with 30+ common pathogens CE mark approved for sale in Europe Ergonomic, user-friendly extraction tube that minimizes contamination Initial patient care action can begin during the patient’s visit as positive results are visible in as soon as 3 minutes Individually sealed foil pouches containing: One cassette device One desiccant Sample extraction tubes Sample extraction buffer Nozzle with Filter Sterile swabs, each sealed in a plastic-paper pouch Instructions for Use CTK Products at a Glance Flyer Inserts CTK’s Respiratory Rapid Test Range Video