INTENDED USE The Finecare™ NGAL Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Neutrophil Gelatinase-Associated Lipocalin (NGAL) concentration in human urine. The test is used as an aid for the diagnosis of kidney injuries. 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.

The advanced BC-6800Plus not only provides more reliable routine CBC plus 5-part DIFF results, but also has a higher throughput of up to 200 samples per hour. Based on the new SF Cube technology platform, the BC-6800Plus could provide more reliable blood cell results and abnormal cells flagging results with anticipated warning messages, exceeding clinicians’ expectations and setting a new standard for blood analysis. SF Cube Technology With the newly designed opticals and reagent systems, the SF Cube technology can help doctors to better differentiate the clusters of cells, which is the key to revealing more abnormal cells. NRBC result in every CBC In WNB scattergram, BC-6800Plus provides NRBC, Basophils and WBC-N* results. It means that the actual number of NRBCs can be measured in routine CBC, if they are present in the sample. Basophils are counted in this counting channel with NRBC results. Basophil and NRBC results are generated on BC-6800Plus without extra reagent or cost. NLR parameter in each CBC+DIFF 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. More accurate RET and PLT-O result By utilizing the new fluorescent dye, the reticulocytes and platelets are more specific stained with stronger fluorescent signal, that brings more reliable reticulocyte and platelet results. Automatic Rerun & Reflex Should the sample results trigger the criteria, the sample rack can automatically step back for a “rerun” or “reflex” check. 200 test/hour BC-6800Plus can load up to 100 samples at a time and offers a throughput of up to 200 tests per hour.

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.

The BC-5390 is a 5-part Auto Hematology Analyzer that delivers high productivity, better accuracy and improved patient care, without sacrificing your budget. The analyzer utilizes the power of three mainstream technologies: laser scatter, flow cytometry, and chemical dye, to provide more accurate clinical information. The BC-5390 has been approved by FDA. Features Robust capacity and functionality Its throughput of 60 samples per hour saves your time, and the capacity of 40 autoloading tubes can extend your walk-away time. More reliable test result.The new reagent, with better anti-aging capacity, helps better differentiate Eosinophils from Neutrophils in the DIFF scattergram, even on samples with high density of Eosinophils. The analyzer is empowered by the fluid sensing technology to detect clot, bubble and insufficient sample, ensuring accurate sample aspiration. Flexible sample aspiration With different holder adapters, the analyzer supports three analysis modes - venous whole blood mode, pre-diluted mode and capillary whole blood mode. Product Specification Model Name/Number BC-5390 Operation Mode Fully Automatic Usage/Application Hospital Brand Mindray Capacity 40 autoloading tubes Throughput 60 samples per hour

STANDARD Mentor BT The pain associated with blood drawing has been minimized by using an amount of blood as minimal as 0.3 µl, and the stored results can be transferred to the smart phone app via Bluetooth technology. NFC communication is also available for the convenience of the user.Advantage Minimized pain associated with blood drawing with an amount of blood as minimal as 0.3 µl No coding Blood glucose data transfer using Bluetooth 4.0 and NFC communication technology. Specification Enzyme Glucose Oxidase biosensor Measurement Range 10 - 600mg/dL (0.6 - 33.3 mmol/L) Test Time 5 sec Sample Volume 0.3 µl Hematocrit 20 - 60% Unit mg/dL Memory Up to 500 tests Battery 3V battery (CR2032) Interpretation of results Cat. No. Product Component Note 01GC520 STANDARD™ GlucoNavii® CodeFree® Plus BT Blood Glucose Monitoring System Meter, Test Strip (10EA) / Lancet(10EA) / Lancing Device / Check Strip 01GC270 STANDARD™ Mentor BT Blood Glucose Monitoring System Meter, Test Strip (10EA) / Lancet(10EA) / Lancing Device / Check Strip 01GS21 STANDARD™ Mentor Blood Glucose Test Strip STANDARD™ Mentor Test Strip (25EA x 2 bottle)

STANDARD Mentor The pain associated with blood drawing has been minimized because it has been developed to measure accurately even with an amount of blood as minimal as 0.3 µl. About this item Approved Glucometer : FDA and KMFDS Approved, Accuracy Criteria : Its Fulfills EN ISO 15197 : 2015 International Standards. Minimum Blood Sample Needed : 0.3 μl, Memories : Standard Mentor Glucometer allows to save previous and up to 500 test Memories Box Included : Glucometer, 10 Lancets, 10 Strips, 1 Lancing Device, 1 Meter Check Strip, 3V Battery type CR2032, Carrying case, User Instruction Guide, Warranty Card. Pre & Post Meal Mark Alarm, No Coding Glucometer, 99.9% Gold Electrode Strip. Authorized Representative : MT Promedt Consulting GmbH - Altenhofstrasse 80 66386 St. Ingbert Germany. Warranty & Support : Standard Mentor Glucometer comes with Lifetime Warranty and support provided by Standard, For any product queries contact (18001023105). Advantage Minimized pain associated with blood drawing with an amount of blood as minimal as 0.3 µl No coding Accuracy that meets international standards

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.

Autozyme Alkaline Phosphatase 60 Diagnostic Reagent (Pack Size : 12 x 5 ml) from Accurex. Alkaline Phosphatase 60 are used in the diagnosis of hepatobiliary disorders and bone disease associated with increased osteoblastic activity. Alkaline Phosphatase high levels may be a sign of a liver problem or a bone disorder Alkaline Phosphatase 60 reagent is set for determination of Alkaline Phosphatase activity based on kinetic method using p-nitrophenyl phosphate (p-NPP), the reagent is a Highly stable reagent & its activity can be determined in just 2.5 minutes. About Autozyme Alkaline Phosphatase is a reagent set for determination of Alkaline Phosphatase 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 Pack Size : 12 x 5 ml Principle The working solution is stablə for 21 days at 2- 8°C. The working solution should be prepared and stored in the dark (working solution bottle) provided.This is critical because the reagent is light sensitive. It should therefore be kept away from direct light. Alkaline Phosphatase cleaves p-nitrophenyl phosphate (p-NPP) into p-nitrophenol and phosphate. p-nitrophenol is a yellow color compound in alkaline medium and absorbs light at 405 nm. The rate of increase in absorbance at 405 nm. is proportional to Alkaline phosphatase activity in specimen. Quality Control To ensure adequate quality control, it is recommended that each batch should include normal and 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 The kit should be stored at 2-8°C and is stable till the expiry date indicated on the label. The working solutions of Non Prostatic Acid Phosphatase & Total Acid Phosphatases are stable for 7 days at 2-8°C.

Product Description: Fully Automated 5 Part Differential Analyser with continuous loading Product Features: Tri angle laser-based flow cytometry for WBC and differentials enumeration 33 reportable parameters including NLR, P-LCC, P-LCR, Mentzer index and RDWI 20 µl sample volume Throughput 80 samples/ hr Large storage capacity of 100000 samples Bidirectional Interfacing Large coloured LCD touch screen of 22 inch Product Application: CBC + Diff Analysis Mode Type: Whole Blood, Predilute, Capillary Autoloader: 60 Tubes; Continuous Loading with Auto-Mixing 33 Parameters: CBC: WBC, RBC, Hb, HCT, MCV MCH, MCHC, RDW-CV, RDW-SD, PLT, MPV, PCT, PDW-SD, PDW-CV, P-LCR, P-LCC, DIFF: Neutrophils % & #, Lymphocytes % & #, Monocytes % & #, Eosinophils % & #, Basophils % & # *ALY % & #, *LIC % & #, *NLR, *Mentzer index and *RDWI *Research use only Principle of Measurement: RBC/PLT/WBC : Electrical Impedance WBC DIFF: Tri-angle Laser Flowcytometry Hb: Cyanide Free Colorimetry MCV: Measured HCT: Calculated Histograms : 3 (RBC/WBC/PLT) Scattergrams : 3 (2D Scattergram), 1 (3D Scattergram) QR Code Reader: For reading sample bar codes & direct input of QC values Sample Volume: Whole Blood: 20 µL Pre- diluted: 20 µL Capillary: 20 µL CBC Mode : 13 µL Linearity Range: WBC : 0 - 300 ( x 103/µL) RBC : 0 - 300 ( x 103/µL) Hb: 0 - 25.0 (g/dL) HCT: 0 - 67 (%) PLT : 0 - 3000 (x 103/µL) Calibrator: ELite H Cal Tri-level Controls: Erba H5 CON L, N, H Open Vial Stability at 2 - 8˚C: 16 Days Throughput: 80 Tests/Hr Quality Control: 500 files with L-J Graph X- Bar Analysis Data Storage: 1,00,000 Results with Graphs Dimension (mm): 650x550x610 Weight (kgs): 59 Reagents: ELite 580 Dil ELite H580Lyse1 ELite H580Lyse2 ELite H580Lyse3 Elite H Clean Interfaces: 4 USB ports ( for connecting external devices including external printers) + 1 LAN Port (HL 7, TCP/IP; LIS connectivity) Operating Environment Temperature: 15-40˚C Humidity: 30-90% Power Requirement: A.C. 100 - 240 V with built-in voltage stabiliser 50/60Hz, 200 VA