Oscar Troponin-I is an in vitro diagnostic test based on immunochromatographic assay. It is designed for qualitative determination of Cardiac Troponin-I (cTnI) in human serum / plasma as an aid in the diagnosis of acute myocardial infarction (AMI). For professional and in-vitro diagnostic use only. Pack Size: 10 Tests

Troponin-I WHOLE BLOOD RAPID TEST For Qualitative Detection of Troponin-I Whole Blood Rapid Test Type : Device Pack Size : 25 T

The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Troponin I (cTnI) in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL. It can be performed within 15 minutes by minimally skilled personnel, and without the use of laboratory equipment. The OnSite Troponin I Combo Rapid Test is intended to be used by healthcare professionals as an aid in the diagnosis of acute myocardial infarction (AMI). Any use or interpretation of this preliminary test result must also rely on patient’s symptoms and the professional judgment of a physician. A more precise test method such as an instrument method must be used to confirm the test result obtained by this device. Normally the level of cTnI in the blood is very low. cTnI is released into the blood stream in forms of free cTnI and cTnI-C-T complex at 4-6 hours after myocardial cell damage. The elevated level of cTnI could be as high as 50 ng/mL during 60-80 hours after AMI and remains detectable for up to 10-14 days post AMI. Therefore, circulating cTnI is a specific and sensitive marker for AMI. Clinical performance: Relative Sensitivity: 95.8% (95% CI: 91.5-97.9%) compared to a reference CLIA Relative Specificity: 99.7% (95% CI: 98.8-99.9%) Analytical sensitivity: The detection limit of cTnI is 1.0 ng/mL or greater in serum, plasma or whole blood specimen Cross-reactivity: No cross reactivity with 10 µg/mL skeletal muscle TnI, 2,000 ng/mL cardiac muscle TnT, 20 µg/mL cardiac muscle Myosin Dose hook effect: No hook effect was observed for cTnI at concentrations up to 3,521 µg/mL Interference: No interference was seen with 20 mg/dl Acetaminophen, 20 mg/dl Acetylsalicylic acid, 10.5 g/dl Albumin, 20 mg/dl Ascorbic acid, 1,000 mg/dl Bilirubin, 20 mg/dl Caffeine, 800 mg/dl Cholesterol, 200 mg/dl Creatinine, 20 mg/dl Gentistic acid, 1,000 mg/dl Hemoglobin, 600 mg/dl Oxilic acid, 1,600 mg/dl Triglycerides Shelf life: 24 months Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample diluent (REF SB-R3002, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Insert MedlinePlus: Troponin Test Poster

INTENDED USE The Finecare™ One Step cTn I/CK-MB/Myo Rapid Quantitative Test a fluorescence immunoassay to be used along with Finecare™ FIA System for quantitative determination of cardiac Troponin I (cTn I), MB Isoenzyme of Creatine Kinase (CK-MB) and Myoglobin (Myo) in human whole blood, serum or plasma. The test is used as an aid to the diagnosis of myocardial infarction. STORAGE AND STABILITY 1. Store Finecare™ One Step cTn I/CK-MB/Myo Rapid Quantitative Test at 4 ℃~30 ℃. Do not freeze. Shelf life is up to 24 months, refer to label for expiration date 2. If removed from refrigeration, allow the Test Cartridge for 30 minutes to reach room temperature (25±2℃) before testing. 3. Once opened, commence to use the Test Cartridge within an hour. 4. Do not remove the device from the pouch until ready to use. Keep the Test Cartridges away from light.

INTENDED USE The Finecare™ cTn I/NT-proBNP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of cardiac Troponin I (cTn I) and N-terminal prohormone of brain natriuretic peptide (NT-proBNP) in human whole blood, serum or plasma. This test is used as an aid to assist in the diagnosis of myocardial infarction and suspected congestive heart failure. 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.

Fully Automatic Oscar Om 511 Hematology Analyzer, For Clinical, User Input: Touch Instrument Name Haematology Analyzer Usage/Application All Automation Fully Automatic Brand OSCAR Parameters CBC + 5 Diff Differential Type 5-Part Number Of Chambers 2 User Input Touch / Manual Number Of Parameters ALL Parameters Instrument Type 5 PART Cell Counter Model Name/Number OM-511 Type Of Blood Analyzer Fully Automatic Sample Mode All Method All Throughput 60 Samples Per Hour Display Digital Features Catalogs Attached Sample Volume 15ul Storage 1 Lac Results No. Of Reagents Used 2 Lyse 1 Diluent Accessories Keyboard ,Mouse ,Tubing Set ,Power Adaptor, Print Roll Calibration Automatic / Manual Chamber Type Double Chamber Depth Of Chamber 100un Detector Yes Dilution Ratio 1.0 Loading Pattern Manual Measuring Method Electric Impedance & Cytometric Measuring Principle Electric Impedance & Cytometric Measuring Range 2 SD Measuring Time 52 Sec Number Of Reading Channels 2 Number Of Squares 4 Operating Voltage 220 Power Supply 220 Reagent System Close with RFID Sample Type Whole Blood Slide Size 0.3un Test Volume 15ul Wavelength 546 Weight 20 Kg Zero Setting Blank Aperture Size RBC 80 , WBC 100 , Plt 60 Is It Portable Yes Measurement Range Mm Hr 60 Test Per Hour Portable Yes Reading Chambers 2 Direct Sample Yes Optical System Wavelength Optical Source Flow cell Height 470mm Point Of Care Yes Dimension 365x470x525mm Printer Yes - Internal Humidity 88% Operational Ambient Temperature 37% Atmospheric Pressure 85 kpa User Interface Yes Reliable Yes Minimum Order Quantity 1 Product Description Company : OSCAR MEDICARE PVT LTD Brand : OM-511 CBC 5 Part Hematology Products Specification : The Brand New Autometed 5-Part Differentials hematology analyzer. Try-angular laser scatter + flow cytometry for 5 Part WBC Counting. Whole Blood, Peripheral Blood, Pre-diluted blood. Throughput with 60 Samples / hour. 29 Parameters (Include 4 research Parameters 3 Reagents with orignal QC & Carlibrators

Oscar Typhoid IgM / IgG TEST DEVICE is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane for differential detection of IgM and IgG antibodies to Salmonella typhi (S. typhi) in human serum, plasma or whole blood. For professional use only. Sensitivity: 92% for IgM and 93% for IgG Specificity: 99% for IgM and 99% for IgG Pack Size: 50 Tests

OSCAR Syphilis / TP Test Device is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for qualitative determi- nation of antibodies (IgG/ IgM/ IgA) to Treponema pallidum (TP) a marker for diagnosis of Syphilis. For professional use only. Pack Size: 50 Tests

OSCAR Preg Sign Test Device is a rapid, qualitative, two site sandwich immunoassay for the determination of human chorionic gonadotropin (hCG), a marker for pregnancy, in urine specimens. For professional use only. Sensitivity: The test has been standardized to the World Health Organization International Standard Pack Size: 50 Tests