ADVIA 2400 Chemistry System The right balance of speed and efficiency The ADVIA® 2400 Clinical Chemistry System manages the most demanding workloads and meets high turnaround-time (TAT) goals. Its menu includes methods for testing drugs-of-abuse, therapeutic drugs (TDM) and new assays such as cystatin C and CardioPhase® hsCRP. The ADVIA 2400 Clinical Chemistry System offers: High throughput of up to 2400 tests/hour (1800 photometric and 600 ISE) to manage heavy workloads Rapid, consistent, 2-second cycle time for faster tube speed and test throughput User-defined automatic repeat, dilution, and reflex testing Large onboard reagent capacity and optional concentrated reagents help to minimize intervention demands Refrigerated onboard storage of controls and reagents for extended stability and increased productivity Automation-ready design: no additional hardware required Features & Benefits The ADVIA 2400 Clinical Chemistry System meets today’s high turnaround-time goals with a throughput of up to 2400 tests/hour. In addition to assays for general and specialty chemistries, its menu includes assays for specific protein measurement, drugs-of-abuse testing (DAT), and therapeutic drug monitoring (TDM). Interesting new assays such as cystatin C, HbA1c with automated sample pretreatment, and CardioPhase® hsCRP can now be included in your routine testing. The ADVIA 2400 Chemistry System pushes productivity levels while maintaining the reliability and stability that keep laboratories up and running. A rapid, 2-second probe cycle time maximizes tube speed and test throughput and combines with the system’s efficient automation-readiness to provide the turnaround time needed for high-volume laboratories Superior Speed and Productivity Throughput of up to 2400 tests/hour (1800 photometric and 600 ISE) to manage the heaviest workloads Rapid, consistent, 2-second cycle time Throughput of 200 tubes per hour, even when running three ISE tests and nine photometric tests per sample Automatic Sample Retain technology, auto-repeat, auto-dilution, and auto-reflex testing Automation-ready Point-in-space aspiration enables connectivity to a track. Redundant sample loading provides built-in backup and easy handling of non-routine samples. Direct sampling from track prevents tubes being detained at an analyzer and reduces aliquoting. Minimal Need for Operator Intervention Minimal-maintenance ISEs Large onboard reagent capacity and optional concentrated reagents for fewer interruptions No-maintenance, 37°C incubation oil bath Auto-calibration and auto-QC from refrigerated onboard calibrators and controls Microvolume technology with 32,000 tests onboard and up to 60 days' onboard stability for improved walkaway time. Concentrated reagents for increased maximum capacity. Remote diagnostics and Inter-Laboratory Quality Control (ILQC) options Exceptional Reliability Sample integrity check for icterus, hemolysis, and lipemia Sample probe with automatic clot/clog detection, liquid-level sensing, short-sample detection, and crash protection Advances in onboard reagent stability, calibration frequency, reduction in interferences, and expanded assay linearity

The OnSite HSV-2 IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to herpes simplex virus 2 (HSV-2) in human serum, plasma or whole blood. Unique test that utilizes glycoprotein G2 to differentiate between HSV-1. and HSV-2 that allows for an early start of treatment action. Immediate determination of either acute or chronic infection by detecting and differentiating IgG and IgM anti-HSV-2. High confidence as test is in agreement with market leading European ELISA: 95.3% IgG; 100% IgM. Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation. Small sample volume (10 µL) enables multiple testing on the same specimen without having to re-draw the patient. Initial treatment action can begin during patient’s visit as test results are available in 10 minutes. Easily transported, and can be stored for 24 months, 2-30oC. Individually sealed foil pouches containing: One cassette device One desiccant Capillary tubes (10 µL) Sample diluent (REF SB-R0213, 5 mL/bottle) Package insert (instruction for use) CTK Products at a Glance HSV-1 & HSV-2 Flyer Insert U.S. CDC HSV Homepage: Genital Herpes Fact Sheets WHO: Herpes Simplex Virus Fact Sheets

Buy Accurex H12 Hemoglobin Test Strips Online – for better result & accuracy. These Hemoglobin strips are used with URIT Hemoglobin Meter, for the quantitative measurement of total hemoglobin in capillary and venous whole blood. These hb strips are to be used by health care professionals only, not to be used for patient self-testing. Accurex HB Test Strips come with a pack size of 50 strips. The Accrues test strip utilizes Dry Chemistry Colorimeter Method (Azido methemoglobin Method). Meter’s optical detectors automatically measure the change in the membrane Buy Accurex H12 Hemoglobin Test Strips Online – for better result & accuracy. These Hemoglobin strips are used with URIT Hemoglobin Meter, for the quantitative measurement of total hemoglobin in capillary and venous whole blood. These hb strips are to be used by health care professionals only, not to be used for patient self-testing. Accurex HB Test Strips come with a pack size of 50 strips. The Accrues test strip utilizes Dry Chemistry Colorimeter Method (Azido methemoglobin Method). Meter’s optical detectors automatically measure the change in the membrane Operation Principle: The test strip utilizes Dry Chemistry Colorimeter Method (Azido methaemoglobin Method). When a drop of whole blood is applied to the test spot on the strip, blood immediately disperses within the membrane, contacting the reagent. The meter’s optical detectors avtomatically measure the change in membrane reflectance. The intensity of reflectance is inversely proportional to the hemoglobin concentration. Blood Sample Collection: Fresh or EDTA-anticoagulated capillary or venous whole blood may be used. If an EDTA – treated sample is refrigeratted to come to the room temperature before testing. EDTA treated blood samples should be mixed using end to and inversions at least 8 times prior to use, and should be tested within 24nours Do not use the haemolytic sample anticogulants other than EDTA are not recommended for use. Caution: 1. Same as all diagnostic tests, hemoglobin test results should be evaluated with the specific patient’s condition. Any results demonstrating the inconsistency with the patient’s clinical status should be repeated or supplemented with additional test data. 2. Do not touch the test membrane by hand 3. H12 Hemoglobin Test Strips are one-off product, do not use again Storage & Preparation: 1.H12 Hemoglobin Test Strips should be stored at O C-30 C dry and dark places, 2 C – B C is the best storage environment emperatures recommended. Keep away from direct sunlight and heat, must not be frozen, If the container was stored in refrigerated before first use, please don’t take it back into the refrigerator again after first use. 2. H12 Hemoglobin Test Strips are ready to use. No additional preparation is required 3. Enclosed desiccants with lest strip. Remove only those strips needed for testing. The remaining lest strips should be resealed in their onginal container and used up in 3 months after first use. Do not use lest strips and throw away alter expiry date. 4. Use the strip immediately once taking it out af the container, otherwise the result will be incorrect 5. Do not fold or cut the test strip. 6. Used lest strips cannot be used again, dispose them as normal medical waste Direction for Use Operating Instructions: 1. URIT Hemoglobin Meter, H12 Hemoglobin Test Strip, Lancing Device, and disposable blood taking needle. 2. Test steps: 1) Turn the meter on and input the Code Card. Check the Code Card displaying on the meter to ensure it to match the Code Card printed on the lest strip container. Otherwise, the result is incorrect. 2) Massage the patient’s finger from the knuckle up to the tip to stimulate blood flow. Clean the sample area with alcohol and wipe it dry with a sterile gauze pad. 3) Insert the lest strip into the strip holder with the notched end in first and the hole facing up. 4) Puncture the skin on the lower side of fingertip with blood collection needle, and remove 13-15 TIL of whole biood with capillary or other micro blood collection apparatus. While waiting for the instrument to display the blood drop symbol, quickly add the drops to the test hole on the reagent sheet. Please make sure that the blood drop volume can completely cover the test hole but not overflow the test hole. 5) The meter starts the test automatically after the blood sample disperses Once the lest is in process do nol disturb or move the meter or test strip, or press any key. The test result will display within 12 seconds. Qualtiy Control Procedure: Use only H12 Hemoglobin Test Strip with QC substance to perform QC. The range of QC substance is the numerical range indicated on the label of the QCsubstance or test strips. When to do a QCtest: 1. Whenever you suspect that the meter or test strips are not working properly. 2. If your hemoglobin test results are not consistent with how you feel. Other Info Limitations of test Method: H12 Hemoglobin Test Strip is only suitable for testing fresh or whole capillary blood or whole venous blood containing EDTA anticoagulants. Do not use serum, plasma or arterial blood

Product Description: It’s an advanced analyzer for Complete Hemostasis. This four channel coagulation analyzer redefines the benefits in its class. Erba ECL 412, can perform PT, APTT, Fibrinogen, Thrombin Time , All Factors, Lupus , Protein S, Protein C , Antithrombin III and DDimer. Product Features: Clotting Tests such as PT, aPTT, Fibrinogen, Thrombin time, Factors, Lupus anticoagulant, Protein S performed using Light scatter principle. Protein C, Antithrombin III done by Chromogenic Principle Tests like D Dimer performed using Immuno-turbidimetry principle Interactive touch screen interface Clotting Graph provides details of the clotting test Cuvette and reagent management software Twelve levels of QC with Levy-Jennings Plot- Identifies random and systematic errors Temperature stability at 37 degree C to perform the tests Low Reagent Consumption USB Connectivity CE mark Product Applications: ECL 412 has uses in various routine IVD labs for doing routine PT and aPTT It has application in Blood Banks for Quality Control of Fibrinogen and Factor VIII It is used as Standby to bigger systems, in accredited centers It is used in Research Facilities to perform PT and aPTT on animal samples such as rat, mouse, rabbit, hamsters etc General Specifications: 4 channel semi-automated hemostasis instrument It can perform 4 simultaneous tests of the same parameter Sample id can be 14 digits alphanumeric, with progressive id or custom id options It is also possible to have a second row of assay preparation/incubation during the analysis of the current line, using preparation line option It can run assays in single or duplicate (programmable per assay) Optically detects and automatically moves to the next assay steps and auto starts the measurements Tests principles: Clotting (scattered light at 640nm) Chromogenic (colorimetry at 405nm) Immuno-turbidimetric (turbidimetry at 800nm) Dimensions / Weight: Dimension : 300 x 290 x 90 mm Weight : 3 kgs Environmental requirements: Operating Temperature : 17-32°C Humidity: Max. 80% Relative Humidity, non-condensing Power: Power Supply: 100-240 VAC and 50/60 Hz Power Consumption: 45 Watts In-Rush Power: 150VA or less Calibrations: Up to 6 calibration levels per assay Storage of the active calibration curve Quality Controls: Up to 12 different control names total can be assigned to any given assay Automatic Levey-Jennings plotting Automatic statistics calculation Storage of Quality Control results Stored results: Independent storage allocation in the instrument memory for Quality Control (QC) and patient determinations Up to 600 results for QC determinations (run in duplicate) Up to 900 results for patients (run in duplicate) New results automatically replace the oldest results of the appropriate category past the maximum storage allowance Reaction curves are exclusively stored on the external USB pendrive. Regular backup and file purging is recommended from the USB pendrive to insure rapid operations. (We recommend at least a monthly purge from a computer to back up and remove CH files) USB pendrive , FAT32 formatted

Vitamin B12 Rapid Quantitative Test The Finecare™ Vitamin B12 Rapid Quantitative Test along with Finecare™ FIA Meters is a fluorescence immunoassay quantitative determination of vitamin B12 level in human serum or plasma. The test is used as an aid in the diagnosis of Vitamin B12 deficiency.

INTENDED USE The Finecare™ LH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Luteinizing hormone (LH) in human whole blood, serum or plasma. This test is used as an aid to diagnose the ovulation cycle, premature ovarian failure and gonadal hypoplasia. 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™ 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™ β2-MG Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of β2-MG (Beta-2-Microglobulin) concentration in human plasma, serum or whole blood. The test is used as an aid for the diagnosis of renal disease. 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™ Lp-PLA2 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System for quantitative determination of Lp-PLA2 in human serum, plasma or whole blood. The test is used as an aid to the assessment of the coronary heart disease (CHD) and ischemic stroke. 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.