LED Lifespan is >50,000 hrs :Enormous cost saving Only 1/10th of the power consumption compared to the other Fluorescence Microscope. No UV radiation emission & explosion proof Provison for digital camera with 50/50 beam splitter that eliminates the need to transit between camera and eye pieces Transmitted light is integrated for bright & dark field microscopy and can be upgraded for phase contrast. Categories: Fully Automated Immunoassay Analyzer, Fully Automated Immunoassay Analyzer category, Fully Automated Immunoassay Analyzer instruments Product Description Product Description:- LED Lifespan is >50,000 hrs :Enormous cost saving Only 1/10th of the power consumption compared to the other Fluorescence Microscope. No UV radiation emission & explosion proof Provison for digital camera with 50/50 beam splitter that eliminates the need to transit between camera and eye pieces Transmitted light is integrated for bright & dark field microscopy and can be upgraded for phase contrast. Intoduction:- The LED fluorescence microscope EUROStar III Plus has been precisely tailored to the requirements of indirect immunofluorescence. A camera can be attached directly to the integrated photo tube for capturing digital images. Switching between the ocular and the camera is no longer necessary owing to the convenient 50/50 beam splitter. Euroimmun also offers the highly functional EUROPicture software for displaying and handling of the digital images. Information:- Constant fluorescence excitation due to regulated LED for reliable and reproducible results Long life span of over 50,000 hours, low current consumption and full light intensity immediately after being switched on Environmentally friendly without mercury cLED available as separate module for equipping various other microscopes Screen diagnostics and digital image acquisition using optional camera with EUROPicture software 50/50 beam splitter for microscopy without switching between the ocular and the optional camera

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.

Getein 1180 Immunofluorescence Quantitative Analyzer is used to measure the concentration of biomarkers in human whole blood, serum, plasma, urine, nasal swab, or saliva samples. Getein 1180 Immunofluorescence Quantitative Analyzer (hereinafter called Getein 1180) is an analyzer for processing and analysis of Getein test kits including biomarkers for cardiovascular diseases, renal function, inflammation, fertility, diabetes mellitus, bone metabolism, tumor, and thyroid function, etc. Getein 1180 is used to measure the concentration of biomarkers in human whole blood, serum, plasma, urine, nasal swab, or saliva samples. The results can be used as an aid in clinical diagnosis of laboratory and point-of-care testing. It is applicable in Emergency, Clinical labs, Outpatient, ICU, CCU, Cardiology, Ambulance, Inpatient Wards, etc.

Designed to fulfill the clinical requirements of minimally invasive surgeries, Mindray's HD3 endoscope camera system comes with the advanced 3-chip CMOS sensor, premium optical lens, real-time optimization software and a FHD screen. Through delivering exceptional image quality and user experiences, the HD3 endoscope camera system enables surgeons to focus on their patients, helping facilitate more accurate diagnosis and treatments. HD3 Camera System 3-chip CMOS sensor FHD picture taking and video recording with USB port Advanced parfocal technology 2X optical zoom Focal length: 14mm-30mm Laparoscopes · High-resolution images and outstanding color rendition · Scratch-resistant sapphire lens · Fog reduction function · Autoclavable lens · Compatible with third-party optical fiber cables HS50 Insufflator · Maximum flow rate: 50L/min · Large 7-inch touchscreen · Gas heating function · Smoke evacuation · Automatic flow compensation · Auto-switchover between veress needle mode and trocar mode · Up to 5 insufflation modes, satisfy all insufflation needs HB200L LED Light Source · Equivalent to 300W Xenon light source · Autoclavable light cable · Auto-detection of light guide cable · Light intensity indicator · LED life expectancy: 40,000 hours PV27 FHD Monitor · 1920*1080 resolution · Picture-in-picture mode · Adjustable brightness · Flexible input: DVI,SDI,S-video,VGA

BC-6800 Today, laboratories not only need more reliable routine CBC plus 5-part diff WBC testing by way of high processing speed, but are also looking for options that extend the analyzer's output in form of Reticulocytes, Nucleated RBCs, Fluorescent Platelet counts etc. for wider clinical application and research. On the other hand, they are restricted by limited budgets. BC-6800 can help to meet all these needs just perfectly and even exceed the expectations. Additional parameters for further clinical applications IMG(#,%) parameters provide information about immature granulocyte, including promyelocytes, myelocytes and metamyelocytes. HFC*(#,%) parameters represent high fluorescent cell population, such as blasts and atypical lymphocytes. RET(#,%) extend valuable help in the differential diagnosis and/or therapeutic monitoring of anemias. IRF is parameter concerning immature reticulocytes, which can assist in early diagnosis of anemia and monitoring the bone marrow response to therapy. InR*(#,‰) are parameters regarding infected red blood cell. The red blood cells may infected by plasmodium, which can cause malaria. * means research parameters SF Cube Technology SF Cube is a pathbreaking technology for reliable blood cell analysis, including WBC differential, Reticulocytes and NRBC with efficient flagging. After reaction with proprietory reagents, the targeted blood cells undergo 3D analysis using information from scatter of laser light at two angles and fluorescence signals. The 3D scattergram builds the power to better identify and differentiate blood cell populations, especially to reveal abnormal cell population undetected by other techniques. Minimizing interference to ensure more accurate results NRBCs are counted in a dedicated channel by SF cube method, which automatically corrects total WBC count and 5-part Diff results when NRBCs are detected. The Focusing Flow-DC method minimizes the interference traditionally encountered in DC technology to produce near gaussian histograms. PLT-O result avoids the interference from microcytic and fragmented RBCs, large platelets and/or platelet clumps by fluorescent stain, and enhances the results accuracy and sensitivity. High automation to minimize the workload Throughput for 125 tests/hour, autoloader for 100 sample tubes capacity Bi-directional LIS with HL7 or ASTM communication protocol Customizable re-exam rules allow users to define their re-exam criterion according to lab’s practice

The new and improved RTR-1 uses an image processing method. During measurement, the lateral flow device is captured using a 5-mega pixel camera and the picture is analyzed using image processing algorithms for identification of either presence or absence of test line bands or test line band intensity levels. The reader converts the image into a grayscale and then classifies the intensity levels of the image in 0 to 255 grayscale range. The image processing algorithm undergoes various levels of filtering and segmentation to yield the correct intensity levels from the picture. Based on the preconfigured intensity levels, the reader classifies the band intensity and reads out the results as either positive or negative. ACCURACY: Less than 3% intra-run CV Eliminates subjective interpretation by operator FLEXIBILITY: Single mode for low volume test setting Batch mode allows for high volume test setting Result output as semi-quantitative line intensity and visual image EASE-OF-USE: Built in barcode reader provides faster test setup Touch screen interface for easy operation Lightweight (0.7kg) and portable DATA MANAGEMENT: Results presented on screen, on a printout or uploaded to reader database Storage capacity of 1,000 test results (including images) Laboratory Information System (LIS) and Wi-Fi compatible Human Machine Interface 4-inch resistive touch screen Camera 5 mega pixel CMOS camera Barcode Scanner Integrated 1 dimensional barcode scanner Printer 48 mm inbuilt thermal printer Mode Single mode and batch mode operations Port/USB Data export and software upgrade through 2 USB ports Storage Storage capacity of 1000 test results (including images) Result output “Positive or Negative” as well as quantitative test line intensity Power 12V 2A Processor ARM Cortex-A53 Platform Embedded Linux Dimension 220 mm X 170 mm X 110 mm (L x B x H) Weight 0.7 kg (Approx CATALOG # PRODUCT RTR-1 Rapid Test Reader OTHER PRODUCTS YOU MIGHT BE INTERESTED IN.. CATALOG # PRODUCT ADX-110 ELISA Reader ADX-120 Microplate Washer

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 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.

Autozyme Alkaline Phosphatase 300 Diagnostic Reagent from Accurex (Pack Size : 30 x 10 ml). Alkaline Phosphatase reagent is used for determination of Alkaline Phosphate activity based on kinetic method using p-nitrophenyl phosphate (p-NPP). Alkaline Phosphatase is a single reagent system using one step procedure & Alkaline Phosphatase activity can be determined in just 2.5 minutes & is is a Highly stable reagent. Alkaline Phosphatase cleaves p-nitrophenyl phosphate p- NPP in the presence of magnesium ions to form p nitrophenol & phosphate. About Method – p-NPP-DEA Buffer – Kinetic reaction with 60 seconds lag phase – Easy reconstitution : Tablet + Diluent – High liquid stability : 21 days Autozyme Alkaline Phosphatase is a reagent set for determination of Alkaline Phosphate activity based on kinetic method using p-nitrophenyl phosphate (p-NPP) Autozyme Alkaline Phosphatase is a single reagent system using one step procedure Autozyme Alkaline Phosphatase has one step reconstitution. It involves dissolving substrate tablet in diluent Autozyme Alkaline Phosphatase is a Highly stable reagent Autozyme Alkaline Phosphatase activity can be determined in just 2.5 minutes Principle Alkaline Phosphatase cleaves p-nitrophenyl phosphate p- NPP) in the presence of magnesium ions to form p nitrophenol and phosphate. The intensity of the yellow color formed is directly proportional to the Application alkaline phosphatase activity in the specimen and measured kinetically. Quality Control To ensure adequate quality control, it is recommended that each batch should include normal and an abnormal commercial reference control serum. It should be realized that the use of quality control material checks both instrument and reagent functions together. Factors which might affect the performance of this test include proper instrument function, temperature control, cleanliness of glassware and accuracy of pipetting. Other Details Two liquid reagent systems. Stable till the expiry date indicated on the label when stored in 2-8°C.