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Medical Equipment

In compliance with out-of-hospital patient transport standards such as EN1789, EN13718-1, IEC60601-1-12 and U.S. military standards, N1 is a highly competent solution for various out-of-hospital transport settings both on land and in air. The N1's exceptional reliability and strong performance enhance your confidence to provide seamless patient care during transport no matter intra or out of hospital. One monitor, Multiple solutions Mirror Mode Two-way screen or remote control functionality and viewing on both the 19" external display and the N1 unit - simultaneously. benevision-n1-fig2-2-pc BeneVision N1 as a Transport Monitor Enhanced data analysis greatly improves parameters' accuracy and anti-interference ability. Its fully integrated sidestream CO2 module monitors the patient's breathing situation by connecting with sampling line directly, freeing caregivers from the shackles of expanding external modules for transport. One monitor, Multiple solutions Mirror Mode Two-way screen or remote control functionality and viewing on both the 19" external display and the N1 unit - simultaneously. benevision-n1-fig2-2-pc BeneVision N1 as a Transport Monitor Enhanced data analysis greatly improves parameters' accuracy and anti-interference ability. Its fully integrated sidestream CO2 module monitors the patient's breathing situation by connecting with sampling line directly, freeing caregivers from the shackles of expanding external modules for transport. benevision-n1-fig2-1-pc BeneVision N1 as a Multi-Parameter Module Slide directly into the module slot or SMR of the N-Series monitor providing an expansive set of parameter measurements. When combined with our additional advanced parameter modules, this solution fits even the highest level of critical care environments. benevision-n1-fig2-3-pc Companion Mode Connect with N-Series host monitor via cable connection to N1 dock and have the ability for dual-screen monitoring and bi-directional control of the bedside monitor - expanding slot space for more advanced parameters and enhanced ICU workflow. Patient-Centric Data Collection When connected to a bedside patient monitor, advanced parameters collected from the host monitor such as AG and BIS, etc., will also be stored in N1 with trend data and alarm events reviewable even when it is disconnected.

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Clinical Chemistry

Best Fully Automated Clinical Chemistry Analyzer – Sphera M from Accurex. This chemistry analyzer is made in Italy & provides Accurate, Precise and Rapid Testing Solution. Sphera M is a Compact, fully automated, open random-access analyzer. The Minimum reaction volume is 210 µl, Minimal < 1L/h water consumption, 80 reusable UV transmitting Bionex® plastic cuvettes, 8-step wash station. It has Removable refrigerated tray with 30 open reagent positions for 50 ml or 20 ml bottles. Multiple virtual reagent disks can be programmed. The Chemistry analyser also does Auto-wash of inner & exterior probe surface. QUALITY CONTROL & CALIBRATION QUALITY CONTROL: • Levey-Jennings plots and Westgard multi rules • Upto 3 QC levels per test • QC monitor and reports • Method statistics: Test counter, CV%, mean, graphical trend analysis CALIBRATION: • Method and reagent monitor (volumes, available tests, calibration, QC status) • Automatic pre-dilution for calibrators • Upto 8 calibrators per method • Auto recalculation of result using last calibration. UNIQUE SOFTWARE DESIGN AND ARCHITECTURE: • Software designed for touch screen use • Intuitive user interface • Continuous loading of samples and reagents • Random-access and STAT • Free choice of execution order • Extended walk-away capability • Results archive with cumulative charts • Programmable automatic start up routine • Multiple work lists INTERFACE: • Bi-directional LIS, ASTM, over ethernet port of the external PC • Positive identification of samples with internal barcode reader (optional) • Printing on any Windows 7®/8® compatible printer • Method defined washing programs SYSTEM PACKS FOR SPHERA™ Accurex has developed dedicated system packs for Sphera™. Our biochemistry reagents have been intensively evaluated and validated to achieve the highest performance in Sphera™. Accurex recommends the use of these system packs according to instructions and applications validated by Accurex. Safety Information 8-step wash station for thorough cleaning of each cuvette (Needles: 6 dispensing, 6 aspiration, 1 cleaning) • Two types of systemic and special washing solutions for removing obstinate probe residues Direction for Use QUALITY CONTROL • Levey-Jennings plots and Westgard multi rules • Upto 3 QC levels per test • QC monitor and reports • Method statistics: Test counter, CV%, mean, graphical trend analysis CALIBRATION • Method and reagent monitor (volumes, available tests, calibration, QC status) • Automatic pre-dilution for calibrators • Upto 8 calibrators per method • Auto recalculation of result using last calibration Other Info Accurex has developed dedicated system packs for Sphera™. Our biochemistry reagents have been intensively evaluated and validated to achieve the highest performance in Sphera™. Accurex recommends the use of these system packs according to instructions and applications validated by Accurex.

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Clinical Chemistry

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

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Biochemistry Analyzer

Yumizen CA40 Semi-automated Clinical Chemistry Analyzer: Yumizen CA40 is a semi-automated Clinical Chemistry analyzer with facility to perform Chemistry, Immunoturbidimetry and Coagulation Tests (PT & APTT). It is an ideal solution for small laboratories with the facility to perform a wide range of biochemical tests. Specification:- Semi-automated Clinical Chemistry analyzer with coagulation tests capacity (PT & APTT) 8 incubation positions for chemistry tests and 5 positions for coagulation tests 8-inch colored touch screen display Tri-level Quality Control with Levey-Jennings chart 6 filters with additional 2 open positions Show less

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immunoassayReagents

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.

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immunoassayReagents

INTENDED USE The Finecare™ S100β Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of S100β in human serum, plasma or whole blood. The test is used as an aid to the assessment of the level of cerebral injury. 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.

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immunoassayReagents

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.

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Intended Use The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C virus in human serum or plasma. It has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigen. Salient Features Based on “Flow Through Technology”, which is similar to Elisa technology because of involvement of washing steps at various levels to enhance the specificity. Use of highly purified HCV antigens for Core, NS3, NS4, NS5 immobilized on the device. Detection of all the subtypes of HCV. Results within 3 minutes. In built quality control dot which validates the test. 100% Sensitivity & 98.9% Specificity as per WHO evaluation. Shelf life : 24 months at 2-8°C

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