Intended Use Dengue NS1 Antigen self-test is a rapid solid phase immune-chromatographic test for the qualitative detection of Dengue NS1 Ag in human whole blood/serum/plasma. This test is intended to be for home use with self-collected whole blood specimens from individuals aged 18 years or above( or collected by adults for individuals below 18 years of age) as well as for professional use with venous Whole blood/Serum/Plasma samples. This test is for in-vitro diagnostic use only & is designed as an aid in the early diagnosis of dengue infection patients with clinical symptoms. Salient Features Rapid, Visual, Home test for qualitative detection of Dengue NS1 antigen detection in human whole blood/serum/plasma. Finger prick sample can be used. Single test pack. All material to perform the test & its disposal are provided with the kit. Based on Sandwich principle.\ Detection of Dengue in Seronegative stage i.e. from Day 1 of fever. Detection of all 4 serotypes of dengue virus. Reliable diagnosis of both primary and secondary infection. 100% Sensitivity & 100 % Specificity. Shelf life: 30 month at 2-30 °C.

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 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.

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 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.

Xpress A1c strips are used for a testing of quantitative determination of glycated hemoglobin(HBA1c) in human whole blood. It is used to monitor metabolic control in diabetic patients. it helps in diagnosis of the diabetes or pre-diabetes in adults. Buy Xpress A1c strips online (Pack of 25 Strips) – the best a1c test strips from Point of Care (POC) Range of Accurex HbA1c strips works as both a pipette and measuring element. A Blood drop of 8uL is needed for measurement. This blood is drawn into the cavity by capillary action. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes. The Xpress A1c strips works as both a pipette and measuring element. A Blood drop of 8uL is needed for measurement. This blood is drawn into the cavity by capillary action. The Xpress A1c strips then needs to be inserted into Xpress A1c meter for hemoglobin measurement, The Xpress A1c meter measures the absorbance of whole blood at Hb isosbestic point. Xpress A1c meter uses two wavelengths of light to calculate Hemoglobin level, user level calibration is not required. How to use: Step 1: Wash hands using soap and warm water. Rinse and dry thoroughly. Step 2: Turn on the meter by pressing-releasing the power button. Step 3: Remove an Xpress A1c strip from the vial. Step 4: Prick a finger to obtain a blood sample. Step 5: Touch and hold the drop of blood to the pointed edge of the Xpress A1c strip. The blood is drawn into the Xpress A1c strip by capillary action Step 6: Once the blood fills the Xpress A1c strip chamber. Insert the Xpress A1c strip into the Xpress A1c meter. Step 7: Your Hemoglobin result will appear on the display window. Step 8: Remove the Xpress A1c strip from the meter and discard it. The meter will automatically turn off or long-press the power button to turn off. The Xpress A1c strips are used to quantitatively measure the concentration of HbA1C in whole blood, suitable for the self-monitoring of HbA1C for diabetes patients. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes. is used to quantitatively measure the concentration of HbA1C in whole blood, suitable for the self-monitoring of HbA1C for diabetes patients. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes.Features: Sample Type: Whole Blood/EDTA Blood/Capillary Blood Measuring Range: 0 to 25 g/dl Temperature: 0°C-50°C Storage Temperature: Room Temperature Expiry: Long Expiry(min 02 yrs) Pack Size: 25 Test/Vial LIMITATION AND WARNING: 1. This product is used for In Vitro Diagnostics only, not for in vivo use. 2. This product should not be used past the expiration date. 3. If there is evidence of microbial contamination or browning, discard the vial. 4. This product is not intended to be used as an HbA1c standard. 5. Preservatives contained in the control, rinse with water if splash into the mouth or eyes, and seek medical help as soon as possible. 6. Potential biological risk. Direction for Use This product should be run in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. (1) Dissolution: Open the cap of the vial, and then add 2 drops of Buffer A. Close the cap, and slightly shake the vial until the powder dissolved completely. And please shake it well before using it. (2) Testing in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. Please refer to the B Storage: 1. This product will be stable for 24 months when stored tightly capped at 2-8℃. 2. After dissolved, the product can be stable for 8 hours at 10-30℃, or 5 days at 2-8℃. Do not freeze it. COMPOSITION: This product is prepared from human blood and contains normal hemoglobin, preservatives and stabilizers. The control is provided in lyophilized powder form for increased stability. The kit contains two levels of control, level 1 is with yellow cap, and level 2 is with green cap.

INTENDED USE The Finecare™ HbA1c Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Hemoglobin A1c in human blood. The test is used as an aid to monitor long-term glycemic status in patients with diabetes mellitus. 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.

Finecare™ 2019-nCoV Antigen Test Antigen testing indicates the active infection of 2019-nCoV. For areas with limited PCR resources, antigen testing can be used for aiding in the diagnosis of COVID-19 suspect patients.

Intended Use Covid 19 Ag Card Test is designed for in vitro qualitative detection of Covid 19 antigen in human nasopharyngeal, nasal swab specimens. The kit is intended for professional use and as a screening test and is an aid in early diagnosis of SARS COV-2 infection in patients with clinical symptoms. Salient Features Rapid Visual Test for the Qualitative Detection of Covid-19 (SARS-COV-2) antigen in Human nasopharyngeal and nasal swab specimens. Based on Sandwich Immunoassay principle. Results within 20 minutes. Single step test procedure. Evaluated & Validated by ICMR Centre ; Sensitivity -91.5% (<30 CT) & Specificity -100% against RT-PCR. Long Shelf life:30 months at 2-30° C. No Instruments required. Convenient pack sizes . 10T,25T,50T,100T & 200T.