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Hematology

VES MATIC 5 is the next-generation automated module manufactured by Diesse Diagnostica (Italy), a highly advanced, Intelligent, Intuitive & Interactive Graphic user Interface for estimating ESR using EDTA samples. Product Features: Automated instrument for the determination of ESR directly from EDTA vacutainers Faster TAT by loading 216 sample tubes at a time Pediatric samples can be processed in microtainers Reliable results with Temperature correction facility Accurate results by eliminating manual HCT correction in Anaemic samples Real-Time monitoring of samples Detection of Lipemic, Hemolyzed, Coagulated samples Standardization in mixing with Inbuilt Mixer Analyser P. Code Product Name Pack size Vesmatic 5 165941 Next 5K Transponder 1x 5000 Vesmatic 5 165942 Next 10 K Transponder 1x 10000 Display - 19" Full HD (1920x1080) LCD with PCAP Touch Screen Peripheral Control - based on Everex distributed control system with peripheral motor control boards Operating system - Linux Analysis module - 89 Positions for Sample Tubes Sample Loading - up to 18 racks simultaneously Throughput - 190 samples per hour. First result after 28 minutes Walk away mode - Supported Continuous loading - Supported Sample mixing - with multiple 180° rotations of the tubes Collection of analysed samples - reinserted into the original loading rack LIS Connection - Multiple LIS connection protocols are available: ASTM / Proprietary Remote diagnostics - available via Ethernet connection. Printer -Alphanumeric with 58mm-wide thermal paper, 36 characters per line, speed 20 mm/sec. Imaging System - 2 high resolution cameras for sample identification and analysis; 1 standard camera for internal inspection Image processor - Dedicated Quad Core CPU with integrated GPU for real-time HD image processing of samples Temperature range in operation - from +15 to + 35°C; Storage from + 5°C to + 45°C Humidity range - from 20% to 80% without condensation Central unit - Quad core ARM Cortex A-53 CPU ARM Cortex A-53, 16 GB eMMC, 4 GB RAM Interfaces - 2 x RS232C, 2 Host USB, 1 Client USB, Ethernet Protection category - CLASS I Safety standard - EN 61010-1, EN 61010-2-081, EN 61010-2-101 EMC - EN61326-1 Installation category - II Mains voltage - 230VAC@50Hz; US/Canada: 110-120Vac@60Hz Electrical energy consumption - 420VA Fuse block - 2 x 5.0 AT (delayed) (5 x 20 mm) UL Dimensions (mm) - 850 (W) x 750 (H) x 830 (D) Weight - 80 kg

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Rapid Test

The OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood. Uses serum, plasma or whole blood specimen Utilizes recombinant antigen derived from the CHIK structure protein IgM immunoassay is the most practical lab method Distinguish from dengue infection which presents with similar symptoms Clinical performance: Sensitivity: 90.4% Specificity: 98.0% comparing to a commercial ELISA Cross-Reactivity: no cross-reactivity found on 10-40 specimens from the 14 disease states and special conditions, such as dengue, Zika, malaria, HIV, TB, HAV, pregnant woman and others No interference with some common substances, such as Acetominophen (20 mg/dL), Heparin (3000 U/L), Ascorbic acid (20 mg/dL), Human IgG (1000 mg/dL), Bilirubin (20 mg/dL), Glucose (55 mmol/L), Creatinine (442 μmol/L), Salicylic acid (4.34 mmol/L), EDTA (3.4 μmol/L), Sodium citrate (3.8%) Individually sealed foil pouches containing: One cassette device One desiccant Capillary tubes (5 μL) Sample diluent (REF SB-R0066, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Inserts U.S. CDC Chikungunya Virus Homepage: (Transmission, Prevention, etc.) WHO: Chikungunya Virus Fact Sheets

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Rapid Test

The OnSite Leptospira IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay that can be performed within 15-20 minutes by minimally skilled personnel, and without the use of laboratory equipment. This test is intended to be used for the simultaneous detection and differentiation of IgG and IgM antibodies to Leptospira interrogans (L. interrogans) in human serum, plasma or whole blood. It is intended to be used as a screening test by professionals, and provides a preliminary test result to aid in the diagnosis of infection with L. interrogans. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Recommended for use: Any person presenting with clinical signs or symptoms consistent with acute infection with interrogans including: high fever, headache, chills, muscle aches, vomiting, jaundice, red eyes, abdominal pain, diarrhea, skin rash After exposure to a known contaminated source Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 μmol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 μmol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant 5 μL capillary tubes Sample diluent (REF SB-R0101, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Inserts U.S. CDC Leptospira Homepage: About Leptospira WHO: Leptospirosis Fact Sheets

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Rapid Test

The OnSite Duo HSV-1/2 IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for qualitative detection and differentiation of antibodies (IgG and IgM) to herpes simplex virus 1 (HSV-1) and herpes simplex virus 2 (HSV-2) in human serum, plasma or whole blood. This test can be performed in 10 minutes by minimally skilled personnel without the use of laboratory equipment. This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with HSV-1 and/or HSV-2. The OnSite Duo HSV-1/2 IgG/IgM Rapid Test uses HSV-1 glycoprotein G1 and HSV-2 glycoprotein G2 for the specific detection and differentiation of IgG and IgM antibodies to HSV-1 and HSV-2 in serum, plasma and whole blood. An HSV-1 and/or HSV-2 IgM positive result indicates an active infection, which may be primary or recurrent. An HSV-1 and/or HSV-2 IgG positive result indicates a recent or past infection. However, a negative test result does not preclude the possibility of infection with HSV-1 and/or HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device. Clinical accuracy: 90.6% sensitivity and 91.4% specificity for anti-HSV-1 IgG detection 93.8% sensitivity and 96.0% specificity for anti-HSV-2 IgG detection 85.0% overall agreement for anti-HSV-1 IgM detection comparing to commercial ELISA 100% overall agreement for anti-HSV-2 IgM detection comparing to BBI Panel (PTH202) Positive rate on random clinical specimens:8% for IgG anti-HSV-1 and 4.9% for IgM anti-HSV-1 (n=10,000); 4.6% for anti-HSV-2 IgG and 1.7% for anti-HSV-2 IgM Cross reactivity: no cross reactivity with the following disease states or special conditions, respectively: palladium, H. pylori, Dengue, Malaria, Typhoid, Toxoplasma, Rubella, CMV, hCG, TB, HAV, HBV, HCV, HEV, HIV, ANA, HAMA, RF (up to 1,000 IU/mL) Interference: No interference was seen with Albumin 60 g/L , Hemoglobin 2 g/L, Bilirubin 20 mg/dL, Heparin 3,000 U/L, Creatinine 442 µmol/L, Salicylic acid 4.24 mmol/L, EDTA 3.4 µmol/L, Sodium citrate 8%, Glucose 55 mmol/L Shelf life: 24 months Individually sealed foil pouches containing: One cassette device One desiccant Capillary tubes (10 µL) Sample diluent (REF SB-R0203, 5 mL/bottle) Package insert (instruction for use) Individually sealed foil pouches containing: One cassette device One desiccant Capillary tubes (10 µL) Sample diluent (REF SB-R0203, 5 mL/bottle) Package insert (instruction for use)

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Hematology

Direct testing with EDTA tubes Quick Infra Red scanning Results in 10 mins Dynamic sedimentation curve available Internal barcode reader and thermal printer Bidirectional LIS Categories: Hematology Analyzer , Hematology Analyzer Instrument Description Technical specifications Product Specification Automation Automatic Brand CPC Model Name/Number YHLO Vision Pro Sample Mode Whole Blood Operating Voltage 240 V Weight 10.5 Kg Dimension 352mmx365mmx325mm Printer Built-In Thermal Printer Test Speed 20 min/cycle Mode Cycle and Random Test Tube Requirement EDTA tube with a diameter of 12/1 3mm Display Type LCD Touch Screen Display Size 7 inch Barcode Reader Internal barcode reader LIS Bidirectional Connect Frequency 50 Hz Product Description Key Facts Direct testing with EDTA tubes Quick Infra Red scanning Results in 10 mins Dynamic sedimentation curve available Internal barcode reader and thermal printer Bidirectional LIS

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Hemoglobin Meter

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

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Glycohemoglobin Analysis

Xpress A1c strips are used for a testing of quantitative determination of glycated hemoglobin(HBA1c) in human whole blood. It is used to monitor metabolic control in diabetic patients. it helps in diagnosis of the diabetes or pre-diabetes in adults. Buy Xpress A1c strips online (Pack of 25 Strips) – the best a1c test strips from Point of Care (POC) Range of Accurex HbA1c strips works as both a pipette and measuring element. A Blood drop of 8uL is needed for measurement. This blood is drawn into the cavity by capillary action. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes. The Xpress A1c strips works as both a pipette and measuring element. A Blood drop of 8uL is needed for measurement. This blood is drawn into the cavity by capillary action. The Xpress A1c strips then needs to be inserted into Xpress A1c meter for hemoglobin measurement, The Xpress A1c meter measures the absorbance of whole blood at Hb isosbestic point. Xpress A1c meter uses two wavelengths of light to calculate Hemoglobin level, user level calibration is not required. How to use: Step 1: Wash hands using soap and warm water. Rinse and dry thoroughly. Step 2: Turn on the meter by pressing-releasing the power button. Step 3: Remove an Xpress A1c strip from the vial. Step 4: Prick a finger to obtain a blood sample. Step 5: Touch and hold the drop of blood to the pointed edge of the Xpress A1c strip. The blood is drawn into the Xpress A1c strip by capillary action Step 6: Once the blood fills the Xpress A1c strip chamber. Insert the Xpress A1c strip into the Xpress A1c meter. Step 7: Your Hemoglobin result will appear on the display window. Step 8: Remove the Xpress A1c strip from the meter and discard it. The meter will automatically turn off or long-press the power button to turn off. The Xpress A1c strips are used to quantitatively measure the concentration of HbA1C in whole blood, suitable for the self-monitoring of HbA1C for diabetes patients. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes. is used to quantitatively measure the concentration of HbA1C in whole blood, suitable for the self-monitoring of HbA1C for diabetes patients. It helps users to understand their diabetes control status or to monitor their risk of developing diabetes.Features: Sample Type: Whole Blood/EDTA Blood/Capillary Blood Measuring Range: 0 to 25 g/dl Temperature: 0°C-50°C Storage Temperature: Room Temperature Expiry: Long Expiry(min 02 yrs) Pack Size: 25 Test/Vial LIMITATION AND WARNING: 1. This product is used for In Vitro Diagnostics only, not for in vivo use. 2. This product should not be used past the expiration date. 3. If there is evidence of microbial contamination or browning, discard the vial. 4. This product is not intended to be used as an HbA1c standard. 5. Preservatives contained in the control, rinse with water if splash into the mouth or eyes, and seek medical help as soon as possible. 6. Potential biological risk. Direction for Use This product should be run in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. (1) Dissolution: Open the cap of the vial, and then add 2 drops of Buffer A. Close the cap, and slightly shake the vial until the powder dissolved completely. And please shake it well before using it. (2) Testing in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. Please refer to the B Storage: 1. This product will be stable for 24 months when stored tightly capped at 2-8℃. 2. After dissolved, the product can be stable for 8 hours at 10-30℃, or 5 days at 2-8℃. Do not freeze it. COMPOSITION: This product is prepared from human blood and contains normal hemoglobin, preservatives and stabilizers. The control is provided in lyophilized powder form for increased stability. The kit contains two levels of control, level 1 is with yellow cap, and level 2 is with green cap.

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Glycohemoglobin Analysis

Accurex Xpress A1c Glycohemoglobin Analysis System Kit . The Kit contains HbA1c Meter, 1 Sampler, 1 box of 25 test strips, Buffer A, Buffer B. Glycohemoglobin Analyzer It is used for testing glycohemoglobin concentration as an aid to monitor the risk of developing diabetes & control the status of diabetes. Buy Xpress A1c Meter Kit Online from Accurex Point of Care (POC ) Range – The HbA1c analyzer is specifically designed to be used with the corresponding test strip. HbA1c analyzer Hemoglobin A1C is a common blood test that measures blood glucose levels over the past two to three months. •Glycohemoglobin Analyzer •Handheld HbA1c Meter •Battery Operated •No Pipetting, No Lysing •Lab like Accuracy •Battery Operated •Truly Portable •Voice prompt for •User Guidance • Accurate result with cv <3% •Lab like accuracy with 95% •No interference of HB Variant •No pipetting •No lysing •Reagent: Suitable to store at room temperature (upto 30º C) The Power of HbA1c in your Hand esting Principle: Boronate Affinity Chromatography Testing Parameter: Glycohemoglobin (HbA1c) Measuring Range: 4.0% – 14.0% Precision: CV <3% (HbA1c: 4.0% – 6.5%) Blood Sample: Finger Prick or Venous Blood ( EDTA Anticoagulant) Blood Volume: About 3ul Testing Time: About 5 minutes Data Unit: Set in Advance the Data Unit • NGSP%; IFCC mmol/mol; eAG* mmol/l Voice Prompt: Voice Prompt to Guide the user Data Storage: 1000 Testing Data Data Port: Mini USB data interface can be connected with HIS/LIS; System Thermal Printer Power Required: AAA Battery x 4 Analyzer Dimension: 61.6 x 122.9 x 24.5 mm Screen Size: 47 x 32 mm” Safety Information LIMITATION AND WARNING: 1. This product is used for In Vitro Diagnostics only, not for in vivo use. 2. This product should not be used past the expiration date. 3. If there is evidence of microbial contamination or browning, discard the vial. 4. This product is not intended to be used as an HbA1c standard. 5. Preservatives contained in the control, rinse with water if splash into the mouth or eyes, and seek medical help as soon as possible. 6. Potential biological risk. Direction for Use This product should be run in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. (1) Dissolution: Open the cap of the vial, and then add 2 drops of Buffer A. Close the cap, and slightly shake the vial until the powder dissolved completely. And please shake it well before using it. (2) Testing in accordance with instructions accompanying BioHermes Glycohemoglobin Test Kit and Glycohemoglobin Analyzer. Please refer to the B Other Info Storage: 1. This product will be stable for 24 months when stored tightly capped at 2-8℃. 2. After dissolved, the product can be stable for 8 hours at 10-30℃, or 5 days at 2-8℃. Do not freeze it. COMPOSITION: This product is prepared from human blood and contains normal hemoglobin, preservatives and stabilizers. The control is provided in lyophilized powder form for increased stability. The kit contains two levels of control, level 1 is with yellow cap, and level 2 is with green cap.

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Hematology

A Truly Automated Walkaway ESR Analyzer for Midsize labs (Meets CLSI and ICSH Guidelines) Product Features: Gold Standard Method -Measures all three phases of sedimentation as per Westergren method Dry Technology - No sample & reagent consumption, no waste generation Faster TAT - Throughput of 60 samples/hr Zero consumption cost by using EDTA tubes HCT correction feature eliminates manual correction in Anaemic samples Temperature correction at 18° ensures reliable results No additional cost of Calibration Analyzer Product Code Product Name Pack size ESL 30 122020 SMART CARD 2500 1x 2500 ESL 30 122021 SMART CARD 5000 1x 5000 ype of Sample : EDTA Sample Volume : > 1.5 ml Display : TFT high resolution 640 * 480 dots with LED Backlight Result Cycle Time : < 25 min Measuring Range : 0-140 mm/hr Touch screen : 5.7 inch resistive TFT high resolution Temperature Correction : At 18 Degree HCT Correction : HCT Correction facility available for Anaemic samples QC : Inbuilt Quality Control program with LJ Graphs Quality Control Level : 3 Level QC with LJ Graph QC Data Storage : 250 QC results Sample position : 30 sample position Throughput : 60 samples per hour Sample Consumption : No Type of Mode : Continuous mode STAT Facility : Available Calibration Requirement : No Mixer : Inbuilt Mixer Printer : Inbuilt Printer Barcode reader : Inbuilt Barcode reader Data Storage : 5000 results Operating Temperature : 20 - 30 Degree Celsius Storage Temperature : 15 - 35 Degree Celsius Relative Humidity : Max. 80% RH Power Adapter external : 240V DC , 90W Main supply : 100V-240V AC, 50/60 Hz (input for power adapter ) Dimension (mm) : 550(L) x 500 (W) x 395 (H) Weight : 20 kg (Approx )

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