Intended Use Dengue Day 1 Test is a rapid solid phase immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen and differential detection of IgM and IgG antibodies to Dengue virus in Human serum/plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue infection & presumptive diagnosis between primary and secondary Dengue infection. Salient Features First line testing kit for detecting dengue infection from day 1 using NS1 Antigen & differential detection of IgM & IgG Antibodies. Diagnosis of both Primary & Secondary Infection. Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4). Highly Sensitive & Highly Specific Long shelf life: 30 months at 2-30°C. Convenient pack sizes: 10 Tests, 30 Tests & 50 Tests.

The GLUCOCARD Vital is everything a blood glucose meter should be - fast, accurate and easy to use. A small 0.5 µL sample size in our GO-based test strip platform gives accurate results in as little as 7 seconds. This auto coded meter has a 250-test memory, records 14- and 30-day averaging and is downloadable. Sample volume: 0.5 μL Test time: 7 seconds Meter range: 20-600 mg/dL Results: Plasma referenced Calibration: Auto coding Display: LCD Memory: 250 tests with time & date stamp Averaging: 14- and 30-day averaging Downloadable: Yes

Autozyme Alkaline Phosphatase 300 Diagnostic Reagent from Accurex (Pack Size : 30 x 10 ml). Alkaline Phosphatase reagent is used for determination of Alkaline Phosphate activity based on kinetic method using p-nitrophenyl phosphate (p-NPP). Alkaline Phosphatase is a single reagent system using one step procedure & Alkaline Phosphatase activity can be determined in just 2.5 minutes & is is a Highly stable reagent. Alkaline Phosphatase cleaves p-nitrophenyl phosphate p- NPP in the presence of magnesium ions to form p nitrophenol & phosphate. About Method – p-NPP-DEA Buffer – Kinetic reaction with 60 seconds lag phase – Easy reconstitution : Tablet + Diluent – High liquid stability : 21 days Autozyme Alkaline Phosphatase is a reagent set for determination of Alkaline Phosphate 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 Principle Alkaline Phosphatase cleaves p-nitrophenyl phosphate p- NPP) in the presence of magnesium ions to form p nitrophenol and phosphate. The intensity of the yellow color formed is directly proportional to the Application alkaline phosphatase activity in the specimen and measured kinetically. Quality Control To ensure adequate quality control, it is recommended that each batch should include normal and an 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 Two liquid reagent systems. Stable till the expiry date indicated on the label when stored in 2-8°C.

The HumaStar 300SR is the latest member of HUMAN's clinical chemistry systems. Based on the proven hardware and software quality of HumaStar 100/200 it uses the time-tested system reagent kits of HumaStar 600 with perfectly matching methods, calibrators and controls. Throughput: up to 300 tests/h Sample positions: 60 Reagent positions: 40 Prefilled and validated system reagents 2 kit sizes per assay available Open channels: 3 Low water consumption (< 3 l/h) Intuitive and powerful software Multi-language: English, Spanish, French Intuitive and powerful software > Full traceability to reagents (e.g. lot & bottle), calibrations, users and settings > Searchable result database > Onboard and calibration stability monitoring > Automatic outlier detection and unit conversion > Method specific wash options > Designed for touchscreen Flexible system reagent concept > Plug & run HumaStar system reagents > Ready-to-use and available in two kit sizes > Usable for HumaStar 300SR and HumaStar 600 > Prefilled barcoded reagent bottles > Validated assay settings for highest quality > Up to 56 days reagent onboard stability > High quality reagents “Made in Germany” Eco-friendly ProClean 2.0 Technology > Minimal carry-over – dual solution wash station > Low water consumption – less than 3 l/h > Separation and reduction of biohazard waste Easy and efficient operation > Multi-step cuvette wash station for reaction cuvettes > Pre and post dilution for long walk-away time > Bottle cap holder prevents bottle mix-ups and saves time > Quick user- and service-friendly maintenance HUMAN‘s reagent production facility In Magdeburg, Germany we produce our reagents in accordance with the latest quality standards, guaranteeing consistent quality at the highest level. HUMAN Gesellschaft für Biochemica und Diagnostica mbH Max-Planck-Ring 21 · 65205 Wiesbaden · Germany Tel. +49 6122-9988-0 · Fax +49 6122-9988-100 · e-mail: human@human.de · www.human.de Immune Status anti-Streptolysin-O, Complement C3 and C4, CRP, Immunoglobulins IgA, IgG, IgM Liver Panel Albumin, Alkaline Phosphatase, Bilirubin Total and Direct, Cholinesterase, gamma-GT, GOT (ASAT), GPT (ALAT), Total Protein Kidney Panel Calcium, Creatinine, Cystatin-C, Inorganic Phosphorus, Magnesium, Microalbumin, Potassium, Sodium, Urea/BUN, Uric Acid, Urinary Total Protein Arteriosclerosis Cardiac Risk Assessment Cholesterol, HDL-/LDL-Cholesterol, Homocysteine, Triglycerides Anemia Iron, Total Iron Binding Capacity, Transferrin Pancreatic Tests alpha-Amylase, Lipase, Pancreatic Amylase Water & Electrolyte Balance Albumin, Chloride, Potassium, Sodium, Total Protein Cardiac Panel CK-NAC, CK-MB, GOT (ASAT), GPT (ALAT), Homocysteine, LDH Diabetes Glucose, HbA1c, Microalbumin, Triglycerides, Urinary Total Protein Prostata Acid Phosphatase HumaStar 300SR Broad range of clinical chemist

INTENDED USE The Finecare™ Vitamin D Rapid Quantitative Test along with Finecare™ FIA Meter is a fluorescence immunoassay quantitative determination of total 25(OH) D2/D3 level in human serum or plasma. Results are to be used in conjunction with other clinical and laboratory data to assist the clinician in the assessment of vitamin D sufficiency. STORAGE AND STABILITY 1. Store at 4°C～30°C up to the expiration date. 2. The solid marker bottle can be stored at 2°C～8°C for 28 days after being reconstituted. 3. Do not remove the device from the pouch until ready to use. The Test Cartridges should be used within 1 hour once opened.

Intended Use Advantage Dengue NS1 Ag card is a rapid solid phase Immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen in Human serum /Plasma.This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue Infection. Salient Features Rapid test based on lateral flow technique. Detection of Dengue in the seronegative stage i.e. from Day 1 of fever. Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4). Results with in 20 minutes Longer shelf life : 30 months at 2-30°C. Convenient pack size : 25 tests Sensitivity-96% and Specificity- 98%

Intended Use Dengue NS1 Antigen FP is a rapid solid phase immuno- chromatographic test for the qualitative detection of Dengue NS1 Antigen in human Whole Blood/ Serum/ Plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of dengue infection. Salient Features Rapid ,visual test for the qualitative detection of Dengue NS1 Antigen in whole blood/serum/Plasma. Sample can be taken from Finger prick and sample required is 4µl. Based on Sandwich principle. Detection of Dengue in Seronegative stage i.e From Day 1 of fever. Detection of all 4 serotypes of dengue virus. Reliable diagnosis of both primary and secondary infection. 100% Sensitivity & 99.96 % Specificity. Shelf life: 24 month at 2-30 °C Convenient pack Size: 10 Test. Evaluated By Referral Medical college / Hospitals /Research institutes / Labs.

Intended Use Dengue NS1 Antigen self-test is a rapid solid phase immune-chromatographic test for the qualitative detection of Dengue NS1 Ag in human whole blood/serum/plasma. This test is intended to be for home use with self-collected whole blood specimens from individuals aged 18 years or above( or collected by adults for individuals below 18 years of age) as well as for professional use with venous Whole blood/Serum/Plasma samples. This test is for in-vitro diagnostic use only & is designed as an aid in the early diagnosis of dengue infection patients with clinical symptoms. Salient Features Rapid, Visual, Home test for qualitative detection of Dengue NS1 antigen detection in human whole blood/serum/plasma. Finger prick sample can be used. Single test pack. All material to perform the test & its disposal are provided with the kit. Based on Sandwich principle.\ Detection of Dengue in Seronegative stage i.e. from Day 1 of fever. Detection of all 4 serotypes of dengue virus. Reliable diagnosis of both primary and secondary infection. 100% Sensitivity & 100 % Specificity. Shelf life: 30 month at 2-30 °C.

Semiautomatic Clinical Chemistry & Turbidimetry Analyzer completely managed by microprocessors and equipped with a wide graphic display, 10 position thermostat programmable from 20°C to 40°C. The 3000 Evolution stores up to 120 different test programmers which can be easily programmed. Stable optics and automatic filter selection assures reliable and repeatable measurements. Calculations are performed automatically so that results are displayed or printed out directly in the required measuring unit.