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

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

Accu-Chek® Guide Blood Glucose Meter Surprisingly Clever Diabetes is complex. Your testing doesn’t have to be Item Description Diabetes is complex. Your testing doesn't have to be with the Accu-Chek® Guide blood glucose monitoring system. With a spill resistant SmartPack® vial, a strip that lets you place a small drop of blood anywhere along the end, and an app that automatically logs results to your phone, it's a surprisingly simple way to manage your diabetes. Benefits and Features Simple to log results without a paper logbook - automatically logs results right to a mySugr app on your smartphone Simple to take just one strip - spill-resistant SmartPack vial lets you take one and spill none Simple to dispose off used test strips - push-button strip ejector means you don't have to touch used strips Simple to see, day or night - strip port light for testing in daytime, nighttime or anytime Simple to be more accurate - delivers advanced 10/10 accuracy for reliable results you can trust1,2,3 Meter Specifications Models: Accu‑Chek Guide wireless blood glucose meter Serial number: Unique serial number etched into meter back Sample claims: Capillary: Yes Venous: ROW = Yes Arterial: ROW = Yes Non-fingerstick sample claim ROW: Palm, forearm, upper arm Measuring principle: FAD glucose dehydrogenase (GDH) Measuring time: Less than 4 seconds Measuring conditions: 4°C to 45 °C (39°F to 113 °F) Storage conditions: -25 °C to +70 °C (-13 °F to +158 °F) Hematocrit range: 10 to 65% Humidity range: 10 to 90 % Altitude independence: 0 to 3,094 m (10,150 ft) Memory capacity: Up to 720 measurements with date and time; 32 control measurements Test averages: 7, 14, 30 and 90 days Data transfer wireless connectivity: using Bluetooth Smart Low Energy Dimensions: 80 x 47 x 20 mm (L x W x H) Weight Approximately: 40 g with batteries Display: Large backlit LCD display with full-text capabilities Beep tone: Yes (factory setting ON) Batteries: (2) 3-volt lithium coin cell type CR2032 Auto power off: 15 seconds after removing a test strip; 90 seconds otherwise Blood volume: 0.6 μL Measuring range: 10 to 600 mg/dL Sample types: Capillary, venous, arterial and neonate Sample dosing: Capillary fill function; suitable for AST Test strip stability 18 months after production date: Test strips are stable (even after opening) until the expiry date printed on the test strip vial. Note: Test strip container must be tightly closed after each strip is removed. Storage temperature : 4 °C to 30 °C (39 °F to 86 °F)

Product Description: Medica Corporation’s EasyLyte® analyzer is a completely automated, microprocessor-controlled electrolyte system that uses ISE (Ion Selective Electrode) technology to make electrolyte measurements. The EasyLyte measures combinations of Na+, K+, in whole blood, serum, plasma, or urine. EasyLyte incorporates state-of-the-art electronics and an innovative ergonomic design that differentiates it significantly from competitors. The analyzer also stores quality-control data that is easily accessible. Patient histories are immediately retrievable for evaluation. EasyLyte analyzers combine simple yes/no prompted operation, low maintenance, and high reliability into one economical design. Product Features: EasyLyte is Easy to Use, Easy to Operate, Easy to Maintain The entire menu is driven by 2 simple buttons Results are displayed on LCD screen as well as printouts EasyLyte does 2 point as well as 1 point calibration Facility to analyze different type of samples: whole blood, serum, plasma ,urine samples EasyLyte has capillary and syringe sampling facility EasyLyte has auto probe wiping facility Analysis of electrolytes is done using 100ul of blood and 400ul of diluted urine Rate of analysis 55 secs per sample Analyzer is capable of storing 128 patients data with trilevel QC results Analyzer has modular plug in reagent pack system EasyLyte has facility for auto calibrations with a programmed interval of 4 hrs and also calibration on demand Analyzer has facility to upgrade to a walk away Electrolyte station by use of Auto Sampler It has a built in thermal printer and a RS 232 port for interfacing Product Applications: Sodium - Na, Potassium - K CLIA Classification: Moderate Complexity Sample Type: Whole Blood, Serum, Plasma or Urine Sample Size: 100 µL Whole Blood, Serum, Plasma, 60 µL capillary or 400 µL diluted (1:10) Urine Method: Direct measurement by Ion Selective Electrode (ISE) Measurement Range: Blood Urine Na+: 20 – 200 mmol/L Na+: 25 – 1000 mmol/L K+: 0.2 – 40 mmol/L K+: 1.0 – 500 mmol/L Cl-: 25 – 200 mmol/L Cl-: 25 – 500 mmol/L Li+: 0.2 – 5.0 mmol/L Ca++: 0.1 – 6.0 mmol/L pH: 6.0 - 8.0 Units Display Resolution: Na+: 0.1 mmol/L K+: 0.01 mmol/L Cl- : 0.1 mmol/L Li+: 0.01 mmol/L Ca++: 0.01 mmol/L pH: 0.005 units Test Time: Na/K Na/K/Cl Na/K/Li Na/K/Cl/Ca Analysis time (blood) 55 sec 55 sec 55 sec 60 sec Urine mode Yes Yes Yes No Analysis time (urine) 90 sec 90 sec 90 sec N/A EasySampler Yes Yes Yes No Capillary Samples Yes Yes Yes No Data Storage: Patient Results: up to 128 samples QC Results: up to 20 each Normal, Low, and High Calibration: Automatic or On-Demand Output: 128 x 64 pixel graphic display 24 column thermal printer Serial port (RS-232), EasySampler port Ambient Conditions: 15–32oC (60–90oF), <85% humidity Power: 100-240 VAC 50/60 Hz, 0.8A Size & Weight: 9.5”W x 16.5”H x 8.0”D (24 cm W x 42 cm H x 20 cm D) 13 lbs. (5.8 kg) Reagents used with this 'EasyLyte' CLIA Classification: Moderate Complexity Sample Type: Whole Blood, Serum, Plasma or Urine Sample Size: 100 µL Whole Blood, Serum, Plasma, 60 µL capillary or 400 µL diluted (1:10) Urine Method: Direct measurement by Ion Selective Electrode (ISE) Measurement Range: Blood Urine Na+: 20 – 200 mmol/L Na+: 25 – 1000 mmol/L K+: 0.2 – 40 mmol/L K+: 1.0 – 500 mmol/L Cl-: 25 – 200 mmol/L Cl-: 25 – 500 mmol/L Li+: 0.2 – 5.0 mmol/L Ca++: 0.1 – 6.0 mmol/L pH: 6.0 - 8.0 Units Display Resolution: Na+: 0.1 mmol/L K+: 0.01 mmol/L Cl- : 0.1 mmol/L Li+: 0.01 mmol/L Ca++: 0.01 mmol/L pH: 0.005 units Test Time: Na/K Na/K/Cl Na/K/Li Na/K/Cl/Ca Analysis time (blood) 55 sec 55 sec 55 sec 60 sec Urine mode Yes Yes Yes No Analysis time (urine) 90 sec 90 sec 90 sec N/A EasySampler Yes Yes Yes No Capillary Samples Yes Yes Yes No Data Storage: Patient Results: up to 128 samples QC Results: up to 20 each Normal, Low, and High Calibration: Automatic or On-Demand Output: 128 x 64 pixel graphic display 24 column thermal printer Serial port (RS-232), EasySampler port Ambient Conditions: 15–32oC (60–90oF), <85% humidity Power: 100-240 VAC 50/60 Hz, 0.8A Size & Weight: 9.5”W x 16.5”H x 8.0”D (24 cm W x 42 cm H x 20 cm D) 13 lbs. (5.8 kg)

INTENDED USE The Finecare™ FSH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative measurement of follicle-stimulating hormone (FSH) in human whole blood, serum or plasma. This test is used as an aid to evaluate the ovarian functions in clinical. 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.

INTENDED USE The Finecare™ Prolactin Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative measurement of Prolactin (PRL) in human whole blood, serum or plasma. The test is used as an aid to the evaluation of pituitary endocrine function. STORAGE AND STABILITY 1. Store the test kit at 4～30℃ up to the expiration date. 2. If removed from refrigerator, allow the test for 30 minutes to return to room temperature before testing. 3. Do not remove the cassette from the pouch until ready to use. The test cassette should be used within 1 hour once opened.

INTENDED USE The Finecare™ Estradiol (E2) Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters is for quantitative measurement of Estradiol (E2) in human whole blood, serum or plasma. The test is used as an aid to the evaluation of ovarian diseases. STORAGE AND STABILITY 1. Store the test kit at 4～30℃ up to the expiration date. 2. If removed from refrigerator, allow the test for 30 minutes to return to room temperature before testing. 3. Do not remove the cassette from the pouch until ready to use. The Test cassette should be used within 1 hour once opened.

INTENDED USE The Finecare™ Testosterone Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative measurement of Testosterone in human whole blood, serum or plasma. The test is to be used as an aid in the diagnosis of diseases related to abnormal testosterone levels. STORAGE AND STABILITY 1. Store the test kit at 4~30ºC up to the expiration date printed on the package. 2. If removed from refrigerator, allow the test to return to room temperature for 30 minutes before testing. 3. Do not remove the cassette from the pouch until ready to use. The test cassette should be used within 1 hour once opened.

INTENDED USE The Finecare™ AMH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative measurement of AMH in human whole blood, serum or plasma. The test is mainly used in the assessment of the ovarian reserve and as an aid in the diagnosis of polycystic ovary syndrome (PCOS). STORAGE AND STABILITY 1. Store the test kit at 4~30°C up to the expiration date printed on the package. 2. If removed from refrigerator, allow the test to return to room temperature for 30 minutes before testing. 3.Do not remove the cassette from the pouch until ready to use. The test cassette should be used within 1 hour once opened.