Getein 1100 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 diagnostics of laboratory and point-of-care testing. It is applicable in Emergency, critical care (ICU, CCU), outpatient, cardiology, inpatient wards, clinical laboratories, etc.

Using best-in-class technology, the Mindray CL-6000i is a chemiluminescence immunoassay analyzer with high throughput, high performance and high reliability. Features Throughput: up to 480 tests per hour Measurement principle: enhanced ALP-AMPPD method Reagent carousel: 36 reagent positions with non-stop refrigerating Sample handling: up to 300 samples can be loaded in one batch, sample loading and offloading continuously by sample racks, fast prioritizing STAT samples Sample volume: 5-110 μL Continuously loading of reagents, substrate, cuvettes, wash buffer and waste bags Zero daily maintenance Product Specification Model Name/Number CL-6000i Usage/Application Hospital Brand Mindray Sample Volume Range 5-110 microlitre Throughput up to 480 tests per hour Measurement Principle enhanced ALP-AMPPD method Reagent Carousel 36 reagent positions with non-stop refrigerating Sample Handling up to 300 samples can be loaded in one batch,sample loading and offloading continuously by sample r

We bring forth for our clients an excellent quality of Filter Paper Whatman with the best quality. These papers are processed by making use of optimum quality basic pulp material and advanced technology under the strict industry laid norms. Our offered papers are available in different specifications to meet the requirements of the clients. Product Details: Brand Whatman Type Qualitative Packaging Type Box Shape Round Diameter 110 mm Pattern Plain

High Performance "Full Automated System" Color Touch Panel for good usability 7 inch WVGA color touchscreen with high operability displays measurement results, instrument conditions and operating instructions. "Sample delivery system" enables micro volume samples to be measured As the sample is drawn through the nozzle and delivered correctly and quantitatively to each pad of the strip, the micro volume samples (minimum 1mL) can be measured easily. No cross contaminations are found on the reagent portions despite high sample volume. Sample Urine Test items Glu, Pro, Bil, Uro, Ket, pH, Nit, Bld, Leu, S.G., Alb, Cre(Alb/Cre ratio, Pro/Cre ratio can be calculated), turbidity and color tone Wavelength 5 LED wavelengths (430, 500, 565, 635, 760nm) Measurement principle Test strip :Dual-wavelength reflectance method (One-wavelength for Bld) Specific gravity :Reflection refractometryColor hue :Light-transmission measurementTurbidity :Light-scattering measurement method Test strip AUTION Sticks (10EA & 10PA) , Uriflet S 11UA Reaction time Approximately 60 seconds Throughput 225 samples per hour Strip storage Maximum 400 strips (200 strips x 2 feeder boxes) Required sample volume Normal, STAT measurement: Minimum 2 mL Small volume measurement: Minimum 1 mL Sample consumption Normal, STAT measurement: Maximum 0.90 mL Small volume measurement: Maximum 0.45 mL Sample container Sample tubes (length: 95 - 110 mm, diameter: ø14.0 - 15.8 mm) Maximum sample load 100 samples (Circulation) Data memory Normal, STAT, small volume measurement: 2500 tests Control measurement: 200 tests Check measurement: 50 tests Trouble list: 100 tests Display Large color liquid crystal display (800 × 480 dots) Built-in printer 58-mm width printer paper (24 digits) External output 1 port (Replaceable with the optional Ethernet terminal) Communication method RS-232C compliant (Switchable between one-way and two-way) Measurement environment Temperature: 10 - 30°C; Humidity: 30 - 60% RH (No condensation) Power requirements 100 - 240 V AC (Maximum power line fluctuation of ±10%), 50/60 Hz Power consumption 150VA (Maximum) Dimensions 530 (W) × 530 (D) × 550 (H) mm (including the sampler) Weight Main body: Approximately 36 kg Sampler: Approximately 4 kg

SD CodeFree A representative model of of SD BIOSENSOR which is easy to use and provides accurate results without the need for coding. The SD Codefree Blood Glucose Meter is a compact, hand-held, and easy-to-read monitor that stores up to 500 test results. It provides an accurate picture of your blood glucose level at the time of the test from a small droplet of blood. Specification Enzyme Glucose Oxidase biosensor Measurement Range 10 - 600mg/dL (0.6 - 33.3 mmol/L) Specimen volume 5 sec Sample Volume 0.9 µl Hematocrit 20 - 60% Unit mg/dL Memory Up to 500 tests Battery 3V battery (CR2032) Interpretation of results Cat. No. Product Component Note 01GC110 SD CodeFree™ Blood Glucose Monitoring System Meter, Test Strip (10EA) / Lancet(10EA) / Lancing Device / Check Strip 01GS11 SD CodeFree™ Blood Glucose Test Strip SD CodeFree™ Test Strip (25EA x 2 bottle)

The EUROIMMUN Analyzer I is an open system for fully automated ELISA processing of up to 7 microplates and 180 patient samples in one run. The combination of EUROIMMUN ELISAs and EUROIMMUN Analyzer I enables a quick and simple, but also a secure routine operation, owing to the automatic recognition and allocation of reagents and the import of QC data via Data Matrix codes. A further quality feature is the optionally available climate control unit, which ensures constant incubation conditions — regardless of fluctuating or excessively high laboratory temperatures. The EUROIMMUN Analyzer I is designed for medium to high sample volumes. Fully automated ELISA processing for medium to high sample volume with minimal manual input High reliability and traceability due to automatic identification of barcodes of patient samples and ready-to-use reagents Fast processing of up to 70 tests per hour and up to 7 plates and 180 samples per run Convenient operation of the software including scanning of QC certificates using a 2D-hand barcode scanner Specifications Sample types Plasma, serum, CSF and stool Patient sample capacity up to 180 samples Plate capacity up to 7 Parameter capacity per run up to 54 Shakeable incubators 4 Throughput up to 70 tests per hour Sample tubes Outer diameter 10 – 16 mm, height up to 100 mm Traceability integrated code scanner for identification of samples and reagents User interface Microsoft ® Windows ® 10 Enterprise 2019 LTSC (64 Bit) Online connection ASTM interface, bi-directional Dimensions (WxDxH) 1100 mm x 750 mm x 1000 mm Weight 130 kg

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 Vitamin D Rapid Card Test (10 Tests) Online from Accurex. The Vitamin D test kit consists of 25 AccuTest Vitamin D individually packed test, devices in foil pouches, 25 pipettes for collecting 10 ul of whole blood, 25 lancets, 1 Buffer Vial (Buffer 5 mL) with stabilizers and, thimerosal, 1 Package Insert. Vitamin D Fast test kit is a rapid chromatographic immunoassay for the semi quantitative detection of Vitamin D levels in human blood/serum. This Vitamin D test provides a preliminary screening test result. INTENDED USE AccuTest Vitamin D is a rapid chromatographic immunoassay for the semi quantitative detection of Vitamin D levels in human blood/serum. This assay provides only a preliminary screening test result. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. The performance characteristics of this assay have not been established in a pediatric population. PRINCIPLE AccuTest Vitamin D is based on the principle of a competitive enzyme immunoassay. The assay is based on the competition for 25-OH Vitamin D present in blood/serum sample and Vitamin D present on the test line for fixed number of antibody-gold conjugate. Depending upon the concentration of Vitamin D in blood/serum, there will be free antibody-gold conjugate molecules that will bind to Vitamin D on the test strip and will show a colored line in the test line zone. A control line is present in the test window to work as procedural control. PRECAUTIONS 1. For in vitro diagnostic use only. 2. The test is designed for use with human blood/serum only. 3. Reagents must be at room temperature (8⁰C – 30 ⁰C). 4. Do not use if test device packaging is open or damaged. 5. Do not use the product beyond expiration date. 6. Handle all specimens as potentially infectious. Proper handling and disposal methods should be used according to good laboratory practices. 7. Read test results for 10 minutes as required. Results may deteriorate and may not be consistent after 10 minutes. 8. In order to avoid variable results, mix the blood sample thoroughly. 9. A serum sample subjected to repeated freeze thaw cycles may give variable results Direction for Use PROCEDURE 1. Remove the cassette from the sealed pouch and place it on a hard flat surface with the view window facing up (use the cassette as soon as possible). 2. Using a micropipette, add 10 µl of whole blood or 5ul of serum sample directly into the rectangular specimen well (marked with Red drop) of the cassette. 3. Add 3 full drops of Buffer into the square buffer well of the cassette (Do not move the cassette after addition of buffer). 4. Let the cassette sit for 10 minutes and read your results immediately. Results may deteriorate after the 10 minute mark. Other Info STORAGE AND STABILITY The test device should be stored at 8 ⁰C – 30 ⁰C and will be stable until the expiration date stated on the package. The product is humidity sensitive and should be used immediately after being open. INTERPRETATION OF RESULTS Match the color of the test line with the chart provided.

Buy AccuTest Typhoid IgG/IgM Rapid Card Test (5 Tests) Online from Accurex. The Typhoid IgG/IgM Rapid Test is used for detection & differentiation of anti-Salmonella typhi (S. typhi) IgG and IgM in human whole blood / serum / plasma. This Typhoid test is used as a screening test and as an aid in the diagnosis of infection with S. typhi. Salmonella typhi bacteria causes typhoid Typhoid fever, typhoid symptoms symptoms are likely to develop gradually – appearing one to three weeks after exposure to the disease. There are various typhoid treatment & typhoid vaccine which can be opted after the detetction of Typhoid. Typhoid fever is caused by S. typhi, a Gram-negative bacterium. Worldwide an estimated 17 million cases and 600,000 associated deaths occur annually. Patients who are infected with HIV are at significantly increased risk of clinical infection with S. typhi. Evidence of H. pylori infection also presents an increased risk of acquiring typhoid fever. 1-5% of patients become chronic carrier harboring S. typhi in the gall bladder. The clinical diagnosis of typhoid fever depends on the isolation of S. typhi from blood, bone marrow or a specific anatomic lesion. In the facilities that can not afford to perform this complicated and time-consuming procedure, Filix-Widal test is used to facilitate the diagnosis. However, many limitations lead to difficulties in the interpretation of the Widal test. In contrast, the Typhoid IgG/IgM Rapid Test is a simple and rapid laboratory test. The test simultaneously detects and differentiates the IgG and the IgM antibodies to S. typhi specific antigen thus to aid in the determination of current or previous exposure to the S. typhi. PRINCIPLE The Typhoid IgG/IgM Rapid Test is a lateral flow immunochromatographic assay. The test cassette consists of: 1) a pink-purple colored conjugate pad containing recombinant S. typhi H antigen and O antigen conjugated with colloid gold (Typhoid conjugates) and rabbit IgG-gold conjugates, 2) a nitrocellulose membrane strip containing two test region (Test line M and G) and a control region (control line). The test line ‘M’ is pre-coated with monoclonal anti-human IgM for the detection of IgM anti-S. typhi, test line ‘G’ is pre-coated with monoclonal anti-human IgG for the detection of IgG anti-S. typhi , and the C band is pre-coated with goat anti rabbit IgG. When an adequate volume of test specimen is dispensed into the sample well of the cassette, the test specimen migrates by capillary action across the test cassette. Anti-S. typhi IgM if present in the patient specimen will bind to the Typhoid conjugates. The immunocomplex is then captured on the membrane by the pre-coated anti-human IgM antibody at test region ‘M’, forming a pink-purple line at ‘M’ region, indicating a S. typhi IgM positive test result. Anti-S. typhi IgG if present in the patient specimen will bind to the Typhoid conjugates. The immunocomplex is then captured by the pre-coated reagents on the membrane, forming a pink-purple line at test region ‘G’, indicating a S. typhi IgG positive test result. Absence of any pink-purple line at test region (M and G) suggests a negative result. The test contains an internal control (control line) which should exhibit a pink-purple line of the immunocomplex of goat anti rabbit IgG/rabbit IgG-gold conjugate regardless of the color development on any of the test region. Otherwise, the test result is invalid and the specimen must be retested with another device. PRECAUTION 1. This package insert must be read completely before performing the test. Failure to follow the insert gives inaccurate test results. 2. Do not open the sealed pouch, unless ready to conduct the assay. 3. Do not use expired devices. 4. Bring all reagents to room temperature (15°C-30°C) before use. 5. Do not use the components in any other type of test kit as a substitute for the components in this kit. 6. Do not use hemolized blood specimen for testing. Wear protective clothing and disposable gloves while handling the kit reagents and clinical specimens. Wash hands thoroughly after performing the test. 7. Users of this test should follow the US CDC Universal Precautions for prevention of transmission of HIV, HBV and other blood-borne pathogens. 8. Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled. 9. Dispose of all specimens and materials used to perform the test as biohazardous waste. 10. Handle the Negative and Positive Control in the same manner as patient specimens. 11. The testing results should be read within 15 minutes after a specimen is applied to the sample well or sample pad of the device. Read result after 15 minutes may give erroneous results. 12. Do not perform the test in a room with strong air flow, ie. an electric fan or strong air-conditioning. Other Info STORAGE AND STABILITY Typhoid IgG/IgM test card should be stored at 4-40°C. The card may be stored at room temperature but not exceeding 40°C in the original sealed pouch. The shelf life or expiry of the card is printed on Pouch as well as carton label. The test kit should be kept away from direct sunlight, moisture and heat.