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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.

Based on Mindray’s continuous innovation in hematology field, BC-5130 is especially tailored to assist diagnostic labs who need full CBC + 5-part results, with relatively low daily sample volume, restricted lab space and tight budget. As the lightest and most compact 5-part hematology analyzer so far from Mindray, BC-5130 is a highly user-friendly and innovative analyzer that offers cost efficient CBC and 5-part white cell differential results. It is targeted to fulfill and exceed the demands of our global customers by providing more accurate, more efficient and more innovative solutions for labs. Improved DC impedance technology is used to count and size the RBC and PLT. The smaller counting aperture (50 μm in diameter) provides better performance on samples with low PLT. Efficient Only three routine reagents are required. These have 2 years shelf life and also less consumed by BC-5130. Original QC and calibrator are also provided to ensure the hematology analyzer’s traceability and testing quality. WBC 5-Part differentiation,25 reportable parameters & 23 research parameters,3 histograms Whole blood Mode, Capillary whole blood mode & Prediluted Mode Tri-angle Laser Scatter + Chemical dye + Flow cytometry technology Dedicated optical counting channel for Basophil measurement 10.4 inch large TFT touch screen with user-friendly software Large storage capacity: Up to 1,50,000 samples Throughput:60 samples/Hour Compact Two kinds of lyse reagents are located inside of BC-5130, which helps the small labs to save space. BC-5130, the 5-part hematology analyzer offers a great solution for clinical labs, especially for those who have limited space. Its compact foot-print is a result of innovative technology improvements, including miniaturized semi-conductor laser source, highly integrated electronic boards and optimized liquid handling system. BC-5130 inherits it’s convenient and proven powerful software design from BC-6800 and BC-3600 platforms, the friendly interface is ideal for small sized labs. Running capillary blood through the sample probe directly is more convenient for the users in children’s hospitals, etc. For Prediluted mode, BC-5130 has higher dilution ratio than other 5-part hematology There’s NLR parameter in each CBC+DIFF result. Neutrophil-to-lymphocyte ratio (NLR) is calculated by dividing neutrophil count by lymphocyte count, usually from peripheral blood sample. In laboratory medicine, NLR is used as a marker of subclinical inflammation. According to clinical studies, NLR can be used as a prognostic factor of severe illness in COVID-19 patients. BC-5130 supports bi-directional LIS with test results and patient information. HL7 protocol is supported as well. Technology Compared with traditional helium neon laser or argon laser, semi -conductor laser has smaller size, lower cost and longer life cycle.

GLUCOCARD G+ LINK glucometer You can stay safe about your health by bringing home this Blood Instant glucometer. It delivers accurate results, so you can constantly know what measure to take . It also comes with easy-edge test strips which can freely absorb the blood from your finger. Also, thanks to the WeCheck diabetes management app, it can send your test results to your smartphone. So now no need to give trouble to yourself by manually uploading your results in some third-party apps. Features: EASY WIRELESS SYNCHRONIZATION: Once connected with wecheck management app, results transfer instantly to the WeCheck Mobile App using Bluetooth technology AMAZINGLY ACCURATE: Highly accurate than other devices and provides proper results in some seconds. SHARE HEALTH DATA: You can share your health measurement data easily with your doctors and medical staff via WeCheck App. MOST AFFORDABLE ADVANCED DEVICE: You will get advanced technology with Bluetooth at a very cheaper rate. JAPANESE TECHNOLOGY, MANUFACTURED IN INDIA: Made in India & designed with trusted and advanced technology that ensure accurate results INDIVIDUALLY PACKED TEST STRIPS: Minimizes exposure to humidity, ensuring accurate results and longer shelf life of 18 months AUTO-CODING FUNCTION: Eliminates coding errors, ensuring easy, stress-free & accurate self-testing at home BEFORE & AFTER MEAL RESULT FLAGGING: Flags results as pre & post-meal reading, easy comparison reference for user & doctor RESULT LEVEL INDICATOR: Classifies results in various levels for easy interpretation TEST STRIP SAFE EJECT BUTTON: Safer and cleaner way to dispose of used strip without touching it About WeCheck App: Wecheck App offers many useful functions for diabetic patients, like Blood glucose level management, Insulin, Diet record, Pedometer and Vital Records Control. So you can connect Your device via Bluetooth and it starts recording your health data automatically. WeCheck has another good functionality to convert your records in pdf format, it makes it convenient to show your doctors while regular checkups. By managing data on the cloud You can prevent the loss of valuable data due to smartphone failure or model exchange and restore data smoothly. And You can also share data with family members, close people, and medical staff. Playstore Download Button: https://play.google.com/store/apps/details?id=jp.co.arkray.android.wecheck Apple Store Download Button: https://apps.apple.com/in/app/wecheck-diabetes/id1287838398

Abbott FreeStyle Libre 3 FreeStyle Libre 3 System Next-Gen CGM performance you can count on Now with the smallest, thinnest1 and most discreet2 sensor yet Readings3 are updated 5x faster than other CGMs4 Outperforms other CGMS in connectivity5 Unsurpassed 14-day accuracy, especially in the low glucose range6 Optional, real-time glucose alarms let patients know the minute their glucose is too low6 Performance you can count on With a CGM system that sends real-time glucose readings every minute directly to your patients' smartphones,7 they will be ready to avoid hypos Unsurpassed accuracy 9.2% Overall MARD6 (Adults) and Unsurpassed 14-day accuracy, especially in the low glucose range6 with 93.2% within ±20/20% of YSI values for glucose levels <80 mg/dL and ±20% when ≥80 mg/dL6. No data gaps Now the sensor can store data up to 14 days. So no data gaps means your patients can always retrieve their data even when their smartphone has not synced with their sensor for up to 14 days. Proven clinical outcomes A1c was reduced by 0.55% at 2 to 4 months and sustained for 12 months8 and 50% reduction in serious hypoglycaemia (≤54 mg/dL).9

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.

Buy AccuTest H Pylori AB Rapid Card Test (50 Tests) Online from Accurex. The Helicobacter Pylori is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies to H.pylori in human Whole Blood/Serum/Plasma. H Pylori test provides an aid in the diagnosis of infection with H.pylori. H.pylori is implicated in the etiology of a variety of gastrointestinal diseases, including duodenal and gastric ulcer, non-ulcer dyspepsia and active and chronic gastritis. h pylori symptoms are an ache or burning pain in your stomach (abdomen), Nausea, Loss of appetite, Frequent burping, Bloating & Unintentional weight loss NTENDED USE The H.pylori Antibody Rapid Test Card is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies to H.pylori in human Whole Blood/Serum/Plasma. It provides an aid in the diagnosis of infection with H.pylori. INTRODUCTION H.pylori is implicated in the etiology of a variety of gastrointestinal diseases, including duodenal and gastric ulcer, non-ulcer dyspepsia and active and chronic gastritis. H.pylori infection is found in more than 90% of duodenal ulcer patients and in around 75% of all peptic ulcer sufferers. H.pylori infection is also more common in gastric cancer patients. The risk of gastric cancer has been estimated to be six-fold higher in H.pylori infected populations than in uninfected populations. H.pylori infections occur in human populations throughout the world. In developed countries, about 50% of the population may have H.pylori infection by the age of 60 years, while only 10-20% of adults in the third decade of life have it. Transmission is most probably by the fecal-oral or oral-oral route. Both invasive and non-invasive methods are used to diagnose H.pylori infection in patients with symptoms of gastrointestinal disease. Invasive methods include culture of gastric biopsy samples, histologic examination of stained biopsy specimens, or direct detection of the urease activity in the biopsy (CLO test). These methods need to obtain a biopsy sample by endoscopy.which is expensive,and usually results discomfort and risk to the patient.noninasive techniques include urea breath tests and serological methods. Urea breath test requires expensive laboratory equipment and moderate radiation exposure. Serologic tests are employed to detect antibodies as human immune response to H.pylori, for example the ELISA and the Western immunoblot. The H.pylori Antibody Rapid Test Card detect antibodies to H.pylori infection in human Whole Blood/Serum/Plasma. It is a noninvasive method and does not use radioactive isotopes. The test is easy to perform and requires no specialized equipment. Visual interpretation provides an accurate qualitative result. It is a useful on-site aid in the diagnosis of H.pylori infection. Diagnosis of H.pylori infection by antibody immunoassay can reduce the number of patients requiring endoscopy. PRINCIPLE The H.pylori Antibody Rapid Test Card is an immunoassay based on the principle of the double antigen-sandwich technique. During testing, a Whole Blood/Serum/Plasma specimen migrates upward by capillary action. The antibodies to H.pylori if present in the specimen will bind to the H.pylori conjugates. The immune complex is then captured on the membrane by the pre-coated H.pylori antigens, and a visible pink-purple line will show up in the test line region indicating a positive result. If antibodies to H.pylori are not present or are present below the detectable level, a pink-purple line will not form in the test line region indicating a negative result. To serve as a procedural control, a pink-purple line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred. Safety Information The H.pylori Antibody Rapid Test Card is limited to provide a qualitative detection. The intensity of the test line does not necessarily correlate to the concentration of the antibody in the blood. x The results obtained from this test are intended to be an aid in diagnosis only. Each physician must interpret the results in conjunction with the patient’s history, physical findings, and other diagnostic procedures. x A negative test result indicates that antibodies to H.pylori are either not present or at levels undetectable by the test. Direction for Use TEST PROCEDURE 1. Remove the test cassette from the sealed pouch and use it as soon as possible. 2. Place the test cassette on a clean and level surface. 3. For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma to the specimen well (S) of the test cassette, then start the timer. See illustration below. 4. For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood (approximately 30μl) to the specimen well(S) of the test cassette, then add 2 drops of buffer (approximately 70μl) and start the timer. 5. Read results at 15 minutes. Do not interpret the result after 20 minutes. Other Info STORAGE AND STABILITY x Store as packaged in the sealed pouch at 4-40℃. The kit is stable within the expiration date printed on the label. x Once open the pouch, the test should be used within one hour. Prolonged exposure to hot and humid environment will cause product deterioration.

Product Description: It’s a modern and advanced analyzer in Hemostasis. This single channel coagulation analyzer redefines the benefits in its class Erba. ECL 105 can perform PT, APTT, Fibrinogen, Thrombin Time, All Factiors, Lupus and DDimer. Product Features: Clotting Tests such as PT, aPTT, Fibrinogen, Thrombin time, Factors, Lupus anticoagulant performed using Light scatter principle Tests like D Dimer performed using Immuno-turbidimetry principle Interactive touch screen interface Clotting Graph provides details of the clotting testCuvette and reagent management software Twelve levels of QC with Levy-Jennings Plot- Identifies random and systematic errors Temperature stability at 37 degree C to perform the tests. Low Reagent Consumption USB Connectivity CE mark Product Applications: ECL 105 has uses in various routine IVD labs for doing routine PT and aPTT It has application in Blood Banks for Quality Control of Fibrinogen and Factor VIII It is used as Standby to bigger systems, in accredited centres It is used in Research Facilities to perform PT and aPTT on animal samples such as rat, mouse, rabbit, hamsters etc Key Specifications: Single channel semi-automated hemostasis system It can analyze 1 test at a time Sample id can be 14 digits alphanumeric, with progressive id or custom id options It is also possible to have a second position of assay preparation/incubation during the analysis of the current one, using preparation line option Optically detects and automatically moves to the next assay steps and auto starts the measurements Tests principles: Clotting (scattered light at 640nm) Immuno-turbidimetric (turbidimetry at 800nm) Dimensions / Weight: Dimension : 216 x 205 x 75 mm Weight : ~1 kg Environmental requirements: Operating Temperature : 17-32°C Humidity: Max. 80% Relative Humidity, non-condensing Power: Power Supply : 100-240 VAC and 50/60 Hz Power Consumption : 45 Watts In-Rush Power : 150 VA or less Calibrations: Up to 6 calibration levels per assay Storage of the active calibration curve Quality Controls: Up to 12 different control total can be assigned to any given assay Automatic Levey-Jennings plotting Automatic statistics calculation Storage of Quality Control results Stored Results: Independent storage allocation in the instrument memory for Quality Control (QC) and patient determinations Up to 1000 results for QC determinations Up to 1000 results for patients New results automatically replace the oldest results of the appropriate category past the maximum storage allowance Reaction curves are exclusively stored on the external USB pen drive. Regular backup and file purging is recommended from the USB pen drive to insure rapid operations. USB pen drive, FAT32 formatted

Product Description: It’s an advanced analyzer for Complete Hemostasis. This four channel coagulation analyzer redefines the benefits in its class. Erba ECL 412, can perform PT, APTT, Fibrinogen, Thrombin Time , All Factors, Lupus , Protein S, Protein C , Antithrombin III and DDimer. Product Features: Clotting Tests such as PT, aPTT, Fibrinogen, Thrombin time, Factors, Lupus anticoagulant, Protein S performed using Light scatter principle. Protein C, Antithrombin III done by Chromogenic Principle Tests like D Dimer performed using Immuno-turbidimetry principle Interactive touch screen interface Clotting Graph provides details of the clotting test Cuvette and reagent management software Twelve levels of QC with Levy-Jennings Plot- Identifies random and systematic errors Temperature stability at 37 degree C to perform the tests Low Reagent Consumption USB Connectivity CE mark Product Applications: ECL 412 has uses in various routine IVD labs for doing routine PT and aPTT It has application in Blood Banks for Quality Control of Fibrinogen and Factor VIII It is used as Standby to bigger systems, in accredited centers It is used in Research Facilities to perform PT and aPTT on animal samples such as rat, mouse, rabbit, hamsters etc General Specifications: 4 channel semi-automated hemostasis instrument It can perform 4 simultaneous tests of the same parameter Sample id can be 14 digits alphanumeric, with progressive id or custom id options It is also possible to have a second row of assay preparation/incubation during the analysis of the current line, using preparation line option It can run assays in single or duplicate (programmable per assay) Optically detects and automatically moves to the next assay steps and auto starts the measurements Tests principles: Clotting (scattered light at 640nm) Chromogenic (colorimetry at 405nm) Immuno-turbidimetric (turbidimetry at 800nm) Dimensions / Weight: Dimension : 300 x 290 x 90 mm Weight : 3 kgs Environmental requirements: Operating Temperature : 17-32°C Humidity: Max. 80% Relative Humidity, non-condensing Power: Power Supply: 100-240 VAC and 50/60 Hz Power Consumption: 45 Watts In-Rush Power: 150VA or less Calibrations: Up to 6 calibration levels per assay Storage of the active calibration curve Quality Controls: Up to 12 different control names total can be assigned to any given assay Automatic Levey-Jennings plotting Automatic statistics calculation Storage of Quality Control results Stored results: Independent storage allocation in the instrument memory for Quality Control (QC) and patient determinations Up to 600 results for QC determinations (run in duplicate) Up to 900 results for patients (run in duplicate) New results automatically replace the oldest results of the appropriate category past the maximum storage allowance Reaction curves are exclusively stored on the external USB pendrive. Regular backup and file purging is recommended from the USB pendrive to insure rapid operations. (We recommend at least a monthly purge from a computer to back up and remove CH files) USB pendrive , FAT32 formatted

ECL 760 ECL 760 is an advanced Fully automated coagulation analyzer with seven detection channels providing operators with a compact easy-to-use system. Dedicated for mid-volume throughput labs, the ECL 760 been designed to optimize your productivity. ECL 760 is a blend of modernity and simplicity. Erba reagents oers a wide menu of test parameters for automated coagulation analyzers. KEY FEATURES ECL 760 uses the proven system of percentage intensity of light scatter at 640 nm LED. This optical system ensures early light stability, longer duration usage time and greater lamp life. It minimizes the interference of hemolysis, ictericity and lipemia, in samples at each assay, The system monitors the entire clotting process from reagent addition to complete clot formation with the generation of Clot curve. Clotting Tests  All clotting tests, such as Prothrombin Time, Activated Partial Thromboplastin Time, Fibrinogen, Thrombin time, Factors (II / V / Vll / X / Vlll / IX\ Xl / Xll), Lupus and Protein S are performed. Chromogenic Tests  Chromogenic tests use the colorimetric principle of measuring absorbance of light (405nm LED) by the test in a cuvette. Protein C and Antithrombin Illare some of the tests done by this method. Immunological Assay  The change in light intensity caused by the antigen antibody reaction is detected at 575 nm LED, as the change in the transmitted light.  D Dimer is the most common test performed