Overview A fully automated POC Auto Dry Biochemistry Analyzer called Mispa Chem Dx, With Just 3 to 4 drops (100ul) of whole blood to test up to 19 General and Special chemistry tests in less than 12 minutes. Mispa Chem Dx works on absorption spectroscopy where a change in absorbance is detected by an absorption spectrum and an algorithm is used to calculate the end concentration of the sample in the reagent dry disc. The reagent disc consists of lyophilized reagent beads, diluent, and calibration details in the QR code. The reagent disc contains an intelligent internal quality control system IQC which continuously monitors the disc function to ensure reaction stability and optimal disc performance, IQC is the engine that drives the Mispa Chem Dx accurately and precisely Low Sample Consumption Easy to Use Maintenance Free Accurate Result Disposable reagent disc Sample volume: 100µl Testing time: 12 minutes / sample Temperature: 37°C ± 0.3°C Resolution: 0.001Abs Absorbance: 0-3.0Abs Sample type: Heparinized whole blood, serum, plasma (heparin) QC&Calibration: IQC (Intelligent Quality Control/Calibration） Work condition: Temperature:10-30°C Humidity: 30%-70% Testing method: End point, kinetic, fixed time, turbidmetry etc Light source: 12V/20W, Halogen tungsten lamp with life span over 2500 hours Power supply: AC 100V-240V, 50-60Hz Display: Android 7.0 inch 800*480, multi-point capacitive touch screen Storage: 500,000 results Printer: Built-in thermal printer Interface: 4 USB ports, 1 LAN port Dimension: 315*375*475mm. 4.2kg(N.W.), 7kg(G.W.)

The AUTION ELEVEN AE-4020 is intended for the qualitative and/or semi-quantitative measurement of several physiological markers in urine: Glucose, Protein, Bilirubin, pH, Blood, Urobilinogen, Ketones, Nitrite,　Leukocytes, Creatinine, Albumin, Specific Gravity, P/C (Ratio of Protein to Creatinine) and A/C (Ratio of Albumin to Creatinine). These measurements are used for screening of kidney disease, liver disease, diabetes mellitus and urinary tract infection in general screening populations. Compact Design: 210(W) x 328(D) x 164(H) mm / Approx. 3.6 kg Processing speed: 514 samples per hour (maximum processing mode: 7 second interval) Auto-start function: Measurement starts automatically when a strip is set on the tray. Test strip can be placed either from the left or the right side. Maximum 11 parameters and color tone can be measured simultaneously by special test strips designed and made by ARKRAY. *Some products including test strips may not be available in all countries. Please check with your local Arkray representative or distributor about product availability in your area. Sample Urine Test Strip / Reagent pack AUTION Sticks / Uriflet S / AUTION SCREEN Measurement item GLU, KET, BIL, NIT, PRO, URO, pH, BLD, LEU, ALB, CRE, Specific Gravity, color tone Measurement range Test strip: As Rank table Color tone: As Color tone classification chart Measurement method Test strip method Dual-wavelength reflection photometric method (single wavelength for BLD) Measurement wavelength 4-wavelength LED (430, 565, 635, and 760 nm) Test strip reaction time 60 seconds Processing speed 514 samples per hour (maximum processing mode: 7-second interval) Display Custom LC display (icons are used) Built-in printer 32-digit thermal printer (58 mm width) External output Conforms to RS-232C standard (serial) Option: Ethernet Memory capacity 520 measurement results Temperature correction Auto-correction by the internal temperature sensor (between 10 to 30 °C) S. G. correction Auto-correction by pH values Chromaturia correction Auto-correction by the color tone correction section on test strips Operating environment Temperature: 10 to 30 °C; Humidity: 20 to 80% R.H. (non-condensing) Measurement environment Temperature: 10 to 30°C; Humidity: 30 to 60% R.H. (non-condensing) *Temperature correction function used DC power requirements(To instrument) 12 Vdc 3 A AC power requirements(To AC adapter) 100-240 Vac 50-60 HZ ,1200 mA Voltage fluctuation allowance is ±10% Power consumption Max. 45 VA Dimensions 210 (width) × 328 (depth) × 164 (height) mm Weight Approx. 3.6 kg

The ADAMS A1c, HA-8180T is a fully automated Glycohemoglobin analyzer based on HPLC (High Performance Liquid Chromatography) and is highly effective for ß-thalassemia testing. Measurement speed: 3.5 minutes/test Measurement Item as below HbA2 HbF HbA1c (Stable HbA1c, S-A1c), HbS, HbC, HbE and HbD can be detected. Column design with no more pre-filter change. Color LCD with reagent level, graphs on screen. Samples Whole blood or hemolysis sample Measurement items HbA1c（Stable HbA1c, S-A1c）, HbA2 and HbF (HbS, HbC, HbE and HbD can be detected.） Reagents *1 ELUENT 80A, ELUENT 80B, ELUENT 80CT and HEMOLYSIS WASHING SOLUTION 80H Column *2 COLUMN UNIT 80T Measurement principle Reversed-phase cation exchange chromatography Detection method Dual-wavelength colorimetry (wavelengths measured: 420nm/500nm） Resolution 0.1% Ratio, 1 mmol/mol Measurement range *3 HbA1c : 3-20%, 9-195 mmol/mol HbA2 : 2-10% HbF : 0-100% Guaranteed measurement range *4 HbA1c : 4.2-12.9%, 22-117 mmol/mol HbA2 : 2.4-6.3% HbF : 0.1-14.3% Processing speed 210 seconds per sample Sample consumption Approx.14μL（whole blood） Sample container Blood collection tube （12.3 to 15mm diameter) × ( 75 to 100mm length） Sample cup（500μL） Sampling method Cap-Piercing Rack type ARKRAY racks Number of measurement samples One-way transportation (factory set) : Maximum 50 samples Loop transportation : Maximum 100 samples Column temperature Approx. 39℃ Display Color graphic LCD with backlight Memory capacity 500 test results ( including calibration results ) Built-in Printer Termal printer, 58mm thermal paper External output Serial 1 port (Can be optionally used as an Ethernet port.) Measurement conditions Temperature : 15-30℃ Humidity : 20-80% relative humidity (non-condensing ) Required sample volume Blood collection tube : Minimum 10mm away from the bottom Sample cup : 400μL or more Warm-up time Maximum 30 min. Dimensions 530（W）×530（D）×530（H）mm (Not including the hemolysis washing solution bottle) Weight Analyzer: Approx. 39kg, Sampler: Approx. 4kg Power supply AC100V-240V ±10% 50/60Hz Power consumption Max. 300 VA *1, *2 Reagents and column are sold separately from HA-8180T analyzer. *3 Error-free measurement ranges. *4 Guaranteed ranges for obtaining results equivalent to those from HA-8160 TP mode measurement. ※Design and specications may be changed without prior notice

The ADAMS A1c, HA-8180 is a fully automated Glycohemoglobin (HbA1c) analyzer based on HPLC (High Performance Liquid Chromatography). HbA1c is a good parameter for long-term blood glucose monitoring in patients suffering from diabetes mellitus. Measurement Speed: 48 sec/test for Fast Mode and 90 sec/test for Variant mode. Measurement items are as follows. HA-8180V, Fast Mode HbA1c (Stable HbA1c, S-A1c) and HbF HA-8180V, Variant Mode　 HbA1c (Stable HbA1c, S-A1c) and HbF HbS and HbC separation and HbE and HbD detection can be performed. ・Column design with no more pre-filter change ・Economical - improved aluminium reagents for more efficient reagent supply ・Color LCD with reagent level, graphs on screen Specifications Configuration Main body, sampler (with sample tube spinning unit) and accessories Measurement objects Whole blood or hemolysis sample Column COLUMN UNIT 80 Reagents ELUENT 80A, ELUENT 80B, ELUENT 80CV and HEMOLYSIS WASHING SOLUTION 80H Measurement items Fast Mode HbA1c (Stable HbA1c, S-A1c) and HbF Variant Mode HbA1c (Stable HbA1c, S-A1c) and HbF (HbS and HbC separation and HbE and HbD detection can be performed) Measurement ranges *1 HbA1C: 3 - 20%, 9 - 195 mmol/mol HbF: 0 - 100% Guaranteed measurement ranges *2 HbA1C: 4 - 16%, 20 - 151 mmol/mol HbF: 0.3 - 5% Measurement principle Reversed-phase cation exchange chromatography Measurement wavelength 420 nm / 500 nm (Dual-wavelength colorimetry) Sample supply Sampler Resolution 0.1 % Ratio, 1 mmol / mol Processing speed Variant mode : 90 seconds / test Fast mode : 48 seconds / test Sample consumption Approximately 14 μL (Whole blood) Required sample volume Sample tube : Minimum 10 mm away from the bottom Sample cup : 400 μL or more Sample container Sample tube : (12.3/15 mm diameter) × (75 to 100 mm length) Sample cup: 500 μL Compatible rack type ARKRAY racks Number of measurement samples One-way transportation (factory-set) : Maximum 50 samples Loop transportation : Maximum 100 samples Column temperature Approximately 40°C Warm-up time Maximum 30 minutes Display Large color LCD with backlight Printer For use with 58-mm width thermal printer paper Memory capacity 900 measurement results (including calibration results) External output Serial 1 port (Can be optionally used as an Ethernet port.) Communication system RS-232C compliant (Switchable between one-way and two-way communications.) Transmission speed RS-232C : Selectable from 300, 600, 1200, 2400, 4800, 9600 and 19200 bps Ethernet: 10BASE-T Dimensions 530 (W) × 530 (D) × 530 (H) mm (Not including the hemolysis washing solution bottle) Weight Main body: Approximately 39 kg, Sampler: Approximately 4 kg Power requirements 100 - 240 V AC ± 10 %, 50 / 60 Hz Power input Maximum 300 VA *1 Error-free measurement ranges *2 Guaranteed ranges for obtaining results equivalent to those from HA-8160 VP mode measurement

identi CRP is an immunoturbidimetry monospecific antisera reagent for CRP analysis in serum. Lower detection limit is 0.1 mg/dL. Linearity of the reagent is 22 mg/dL. Reagent is liquid stable and ready to use

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 the Best 5 Parts Hematology Analyzer – ACCULAB CBC 560+. This Hematology Analyser Machine is an advanced and automatic hematology analyzer, comprising 5 parts, 29 parameters, and 3 histograms assay, offers throughput of 60 tests/hour. Features: Tri-angle laser scatter, Flow cytometry method, Impedance method for RBC and PLT counting and Cyanide-free method for HGB test along with 3D holographic scattergram to display the accurate 5 part differentiation of WBC. Equipped with a 14 inch touch screen and large storage capacity for 100,000 results, this hematology analyzer has interface of 4 USB ports, 1 LAN port Bi-direction LIS, support HL 7 protocol, Internal RFID reader. With CBC mode, CBC+DIFF mode, Venous whole blood, Capillary whole blood and Prediluted test mode, this hematology analyzer is an ideal unit for white blood cell counts, complete blood Measuring principle Tri-angle laser scatter, Flow cytometry method, Impedance method for RBC and PLT counting, Cyanide-free method for HGB test Sample volumes CBC+DIFF mode: ≤ 20 μl CBC mode: ≤ 10 μl Throughput 60 tests/hour Assay Items 29 parameters, 3 histograms Display 14 inch touch screen Storage 100,000 sample results, including histograms, scattergrams and patient information Parameter WBC, RBC, HGB, HCT, MCV, MCH, MCHC, RDW-SD, RDW-CV, PLT, MPV, PCT,PDW, P-LCR, P-LCC, NEU%, LYM%, MON%, EOS%,BAS%,NEU#, LYM#, MON#, EOS#, BAS# 4 Research parameter: ALY%, ALY#, LIC%, LIC# Performance Item Linearity range Carry Over CV WBC 0-300 × 109/L ≤ 0.5% ≤ 2.0 % RBC 0-8.00 ×1012/L ≤ 0.5% ≤ 1.5 % HGB 0-250 g/L ≤ 0.5% ≤ 1.5 % PLT 0-3000 × 109/L ≤ 1.0% ≤ 4.0 % Interface 4 USB ports, 1 LAN port Bi-direction LIS, support HL 7 protocol, Internal RFID reader Power Consumption 400 VA Power Supply AC 220V±10%, 50/60Hz, 110V±10%, 60Hz Packaging dimension (W×D×H) 670 × 590 × 790 mm Gross Weight 53 kg Safety Information All the samples, controls, calibrators, reagents, waste and areas contacted with them are potentially biohazardous. Wear proper personal protective equipment (e.g. gloves, lab coat, etc.) and follow safe laboratory procedures when handling them in the laboratory.

Buy the Best Automated Hematology Analyzers – Acculab CBC 360 Neo. This Hematology Analyser Machine is Truly Automated for self-checking, background test, calibration, sampling, dilution, mixing, printing, dormancy, alarms, cleaning and maintenance. CBC 360 Neo is 3 part hematology analyzer from Accurex & is Automated for Walk-away Operations. Dual Chamber: Measurement of RBC / platelets & WBC / HGB in different chambers ensure accurate counting in a short time. The micro-aperture sizes of both the chambers are well designed to avoid error due to cell misclassification Automation for Walk-away Operation: Auto Self-check : Automatic aspiration of reagents & rinsing of tubings on startup Auto Blank : Background test is run automatically on startup Auto Print : Automatic printing of report with / without histogram Auto Sleep : Dormancy status is entered after a set period of non-operation Auto Alarms : Audio / visual alarms in case of system errors & abnormal results Auto Clean : Automatic rinsing options available to maintain the system Dual Chamber: Measurement of RBC / platelets & WBC / HGB in different chambers ensure accurate counting in a short time. The micro-aperture sizes of both the chambers are well designed to avoid error due to cell misclassification Specifications: Measurement principle: Electrical resistance for counting RBC, WBC & Platelets Colorimetric estimation of HGB at 540 nm Parameters: WBC, LY, MO, GR, LY%, MO%, GR%, RBC, HGB, HCT, MCV, MCH, MCHC, RDW-CV, RDW-SD, PLT, MPV, PDW, PCT, P-LCR Throughput: 60 samples/hour Micro-aperture: WBC : 100 um RBC / PLT : 68 um Sample type: Whole blood or pre-diluted sample Sample volume: Whole blood (venous blood) : 10 ul Chamber: Pre-diluent (capillary blood) : 20 ul, Pre-diluent (capillary blood) : 20 ul Reagents: Dual chamber : RBC / Platelets & WBC / HGB Quality control: 4 QC options : L-J, X-B, X-R & X QC, Graphs plotted with 31 data points Data memory: Upto 100,000 (with histogram) Display: 10.4 inch LCD with 640 x 480 resolution Printer: Built-in thermal printer Interface: Support RS-232C, standard network port and USB; keyboard and mouse Operating environment: Temperature : 15˚C – 35˚C, Humidity : 85% RH Electrical specification: Voltage : AC 110V/230V 23V Frequency : 50/60 Hz, Power : 180W Fuse specification : 250V/3A Dimensions / Weight: 670 x 515 x 640 mm / 27.5 kgs Specification Acculab CBC 360 Neo – Fully Automated Hematology Analyzer Features: 3-part differentiation of WBC Automated for — self-checking, background test, calibration, sampling, dilution, mixing, printing, dormancy, alarms, cleaning and maintenance High processing speed : 60 samples/hour Multi-parameter estimation : 20 parameters categorized according to corpuscle type for easy reporting Direct command keys for Mode, Prime, Flush, Drain & Record / Print for faster operation Run / Standby indicator lights denote the analyzer status i.e. test is being run or analyser is ready to test Whole blood/ Pre-diluent indicator lights denote the sample type in use i.e. whole blood/ pre-diluent Dual sample mode with low sample volume: Whole blood (venous) mode : 10 ul; pre-diluent (capillary) mode : 20 ul Audio alarm indication for abnormal findings or system errors 4 QC methods : L-J, X-B, X-R & X QC Comprehensive QC graphs with 31 data points for each parameter Internal & external probe cleaning facility Dormancy mode available to reduce power consumption Memory : 100,000 (with histogram) Safety Information • Large 10.4 inch single screen color display of all 21 parameters and 3 histograms • Sequential arrangement of WBC, RBC & PLT parameters for convenient reporing •Easy to understand & icon-based arrangement of menu for fast and convenient testing Direction for Use • WBC Histogram: R1, R2, R3, R4 & RM indications on histogram show specific abnormalities in the histogram & the probable causes • Platelet Histogram: PM indication is given when the boundary between PLT & RBC is ill-defined thus avoiding misclassification Other Info High voltage cautery function is useful in disintegrating obstinate protein or serum clog in the tubing

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.