With the built-in oxygen concentration monitoring system and effective cable management system, the HyPort R80 is capable of creating a reliable and streamlined ICU environment to ensure patient safety. Recovery The lighting system of the HyPort R80 aims to create a comfortable, near-natural light ICU environment to enhance patient recovery. 1234 1 Circadian Light Simulating 24-hour natural daylight change to reflect circadian rhythm. 2 Examination Light Up to 10,000 lux, 5-level adjustable illuminance meets various needs of head and abdominal examination. 3 Reading Light Effectively avoid invalid glare to meet the reading needs of rehabilitating patients. 4 Navigation Light Providing enough lighting with less glare for medical staff’s easy observation and intervention. Efficiency The HyPort R80 is a highly integrated bedside device management system that helps caregivers organize medical devices to meet various clinical needs. It makes efficient use of beside space with a series of easy-to-use designs, enabling a more efficient workflow for medical staff. Folding-shelf design Suitable for both portable ventilators and integrated ventilators. p46-s3-2-web Bag-valve-mask management Making sure bag valve mask is easy to access and ready for emergency situations anytime when needed. p46-s3-3-web Partition management The pump separation layout allows medical staff to easily identify infusion pumps and feeding pumps. p46-s3-4-web Smooth movement The advanced braking technology ensures stability of the column when moving. NextPrevious Variety The HyPort R80 has been designed to meet the demands of different ICU layouts to create a safer, more efficient and comfortable ICU environment with patient-centric design.ICU double room solution A Product Specification Usage/Application Hospital Brand Mindray Model Name/Number HyPort B80 Features 60 Degreepanel interface for easier plug-in of gas and electricity Color White Panel Interface 60 Degree Product Description Gas and electricity separated 60°panel interface for easier plug-in of gas and electricity Flexible movement of sliding and rotating of the distributions Additional accessories for better management of details Considerate lighting option Safer and more effective workflow Gas and electricity separated 60°panel for easier plug-in of gas and electricity Better management Customized drawer solutions Wire basket - dfferent size options available Cable management solutions

ULTRA Malaria P.F/Pan Ag Ultra Malaria P.f/Pan is an immunochromatographic assay for the differential detection between Plasmodium falciparum Histidine-Rich Protein II (HRP II) and Plasmodium species (Plasmodium falciparum, P.vivax, P.ovale, P malariae) Lactate Dehydrogenase (pLDH) in human whole blood. This test is intended for professional use, only for an initial screening and reactive specimen should be confirmed by a supplemental assay such as microscopic examination of thin blood smear.

ULTRA Malaria P.F/P.V Ag Ultra Malaria P.f/Pv is an immunochromatographic assay for the differential detection between Plasmodium falciparum Histidine-Rich Protein II (HRP II) and pLDH (plasmodium lactate dehydrogenase) specific to Plasmodium vivax in human whole blood.This test is intended for professional use,only for an initial screening and reactive specimen should be confirmed by a supplemental assay such as microscopic examination of thin blood smear.

The OnSite Leptospira IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay that can be performed within 15-20 minutes by minimally skilled personnel, and without the use of laboratory equipment. This test is intended to be used for the simultaneous detection and differentiation of IgG and IgM antibodies to Leptospira interrogans (L. interrogans) in human serum, plasma or whole blood. It is intended to be used as a screening test by professionals, and provides a preliminary test result to aid in the diagnosis of infection with L. interrogans. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Recommended for use: Any person presenting with clinical signs or symptoms consistent with acute infection with interrogans including: high fever, headache, chills, muscle aches, vomiting, jaundice, red eyes, abdominal pain, diarrhea, skin rash After exposure to a known contaminated source Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 μmol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 μmol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant 5 μL capillary tubes Sample diluent (REF SB-R0101, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Inserts U.S. CDC Leptospira Homepage: About Leptospira WHO: Leptospirosis Fact Sheets

Product Details: Wavelength Range 195-1000 nm Display Digital Brand Thermo Sample Compartment 4 Position Cuvette Holder Interface RS-232C Packaging Type Carton Box We are the leading manufacturer of a wide range o These products are UV-VIS Spectrophotometer easy to operate and highly appreciated for its durability. Applications: Microprocessor based UVVIS Spectrophotometer is an analytical instrument that is commonly used in various physics & chemical laboratories to make qualitative and quantitative analysis of under focus materials in the presence of ultraviolet and visible spectrum range. It is widely used in fields such as clinical examination, medicine, petro-chemical industry, biochemistry, bio technology, quality control and environmental protection. It is also used in study at molecular level in of DNA and Proteins. It is non-destructive and easy to use in nature. Salient Attributes of the product: Cover 195 to 1000 nm 4 Position Cuvette Holder RS-232C Computer Interface High wavelength Precision Compact & Good Looking Shape Highly Accurate & Stable

Get the fastest hemoglobin and HCT test within 10 seconds, Buy Accurex URIT-12 Hemoglobin Meter Online. This Hemoglobin tester gives Accurate & Reliable Result. The Urit 12 hemoglobin machine is the best digital hemoglobin Meter with easy 3-step operation. The hb meter is is perfectly fit for the filtration of the numbers of blood donors, POCT, and hemoglobin testing in medical examination center. etc. It works on the prinicple of Optical reflectance. Sample: Capillary or venous whole blood (13~15 ul) & Strips: Accurex H12 Hemoglobin Test Strip URIT-12 is an easy-operation, fast-testing and portable hemoglobin testing Meter, which is perfectly fit for the filtration of the numbers of blood donors, POCT, and hemoglobin testing in medical examination center (MEC) etc. Compared to HiCN-HB method, the results are satisfactory. • Fast hemoglobin and HCT test within 10 seconds • Accurate & Reliable Result • Easy 3-step operation Parameter: Hemoglobin, HCT (Hematocrit) Principle: Optical reflectance Strip: H12 Hemoglobin Test Strip Speed: 10 seconds Sample: Capillary or venous whole blood (13~15 ul) Memory: 250 test results Measuring Range: 4.0g/dL 24.0g/dL(g/L optional) Quality Control: HQ-A Hemoglonbin control solution Calibration: Factory calibrated according to ICSH Power: DC 6V (Two CR2032 Batteries) Automatization: Self-checking, auto-judging and displaying malfunction Dimension: 102mm 50mm 19mm Accuracy: accuracy ≥ 96%,the correlation is very good in the comparison between URIT-12 and ICSH method. Precision: CV < 5%,testing samples including high, medium & low concentration, the CV of 10 repeated test results is 1.8% 2.2% 2.7% respectively. Hematology analyzer is not suitable for the fast and single hemoglobin testing out of the laboratory and the fast hemoglobin filtration for numbers of blood donors, therefore, it’s very necessary to find a kind of method for fast and accurate hemoglobin testing. When a drop of whole blood is applied to the test spot on the strip, blood immediately disperses within the membrane, contacting the reagent. The meter’s optical detectors automatically measure the change of reflectance in membrane. The intensity of reflectance is inversely proportional to the hemoglobin concentration. Other Info Hemoglobin testing is one of the important clinical hemanalysis items. It is useful for the diagnosis of all kinds of anemia. In clinical laboratory, many test items including hemoglobin can be gotten from hematology analyzer.

Buy AccuTest HCV Rapid Card Test (30 Tests) Online from Accurex. HCV means Hepatitis C Virus which is a is a small, enveloped, positive-sense, single-stranded RNA virus. Hepatitis C symptoms are fever, fatigue, decreased appetite, nausea, vomiting, abdominal pain, dark urine, pale feces, joint pain and jaundice. HCV test is a rapid Chromatographic Immunoassay work on principle of the double antigen sandwich technique, Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. AccuTest HCV Test is a rapid Chromatographic Immunoassay for the Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. Hepatitis C Virus (HCV) is a small, enveloped, positive-sense, single-stranded RNA virus. Antibody to HCV is found in over 80% of patients with well documented non-A, non-B hepatitis. Conventional methods fail to isolate the virus in cell culture or visualize it by electron microscope. Cloning the viral genome has made it possible to develop serologic assays that use recombinant antigen, multiple antigens using recombinant protein and/or synthetic peptides have been added in new serologic tests to avoid nonspecific cross-reactivity to increase the sensitivity of HCV antibody tests. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or quest Principle: AccuTest HCV Rapid Hepatitis C Virus Test (Serum/Plasma/Whole Blood) is a lateral flow chromatographic immunoassay based on the principle of the double antigen-sandwich technique. The membrane is coated with recombinant HCV antigen on the test line region of the device. During testing, the serum/plasma or W.Blood specimen reacts with HCV antigen coated particles. The mixture migrates upward on the membrane chromatographically by capillary action to react with recombinant HCV antigen or membrane and generate a colored line. Presence of this colored line indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that the correct volume of specimen has been added and membrane wicking has occurred. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Safety Information •Positive: If a distinct purple line is formed at the test one marked ‘T’ (Test Line) and the Control Zone marked ‘C’ (Control Line) the test result is positive, indicating the sample contains Hepatitis C antibody. The interpretation of test results (+ve for hepatitis) remains unchanged even if there is a difference in intensity of color in positive line and control line as is many a time found. •Negative: If a distinct purple line is formed only at the control zone marked ‘C’ (control line) the test result is negative • Invalid: A total absence of color in both © and (T) regions or no colored band appears on the control © region is an indication of procedure error and/or the test reagent has deteriorated. Repeat with a new test kit. Direction for Use Test Procedure 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Other Info Storage and Stability AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch.

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.