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'unique features analysis endpoint'

Items tagged with 'unique features analysis endpoint'

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Clinical Chemistry

Product Specification Model Name/Number HumaStar 200 Brand Human Automation Fully Automatic Display Digital Dimensions 69 x 76 x 52 cm (WxDxH) Frequency 50/60 Hz Voltage 220-240 or 110-120 Vac Temperature 16-30 Degree C Throughput Up to 200 t/h throughput Weight 51 kg Reaction volume 210-350 il Wash station 6 dispensing needles Water consumption < 2 l/h (8 ml/test) Languages English, French, Spanish Software (other languages can be added) Humidity < 80 % non-condensing Data External computer required (Pentium IV, 2 GHz Mode Open, random-access, STAT Product Description Product Detail : Unique Random-Access Analyzers for Small to Medium Size Laboratories Unique design Unique software architecture Unique features Analysis Endpoint (bichromatic), Differential endpoint (with sample blank), Fixed time, Kinetic (bichromatic) Multi-standard (up to 8), factor, linear, non linear (cubic-spline, poly-linear and logit-log four parameters) Samples Removable sample tray 60 positions: primary tubes 12–12.5x100 mm and 10 mm cups Optional: sample tray for 20 primary tubes 12–16x100 mm and 20 cups 3.5 ml Sample volume: 2–300 µl Internal barcode reader Automatic pre- and post-dilution Test profiles and replicates Reagents Removable reagent tray 30 reagent / diluent positions 50 and 20 ml bottles, adapter for tubes and cups Reagent volumes: 5–350 µl Refrigeration to ~9 Degree C below ambient (at bottom of bottle) Substrates, Enzymatic, Turbidimetric Reaction Reaction volume: 210–350 µl 80 reusable Bionex® cuvettes 6 mm optical path Heat transfer by air Pipetting Needle shock detector Capacitive liquid level detector Wash station 8-step cuvette wash station Systemic and special washing solution HumaStar 200: 6 dispensing needles Water consumption < 2 l/h (8 ml/test) Optical system 9 discrete wavelengths (340, 405, 505, 546, 578, 600, 650, 700 nm, one free position) Band pass: +/– 5 nm Photometric linearity: 0–2.5 Abs Stability: <1 % drift per day Management 20 GB HDD, 512 MB RAM, CD/R, USB) Windows 7® with .NET framework 4.0 English, French, Spanish OS recommended Core i3TM or dedicated graphic card recommended Minimum 900 dots resolution Designed for touch screen (1280x1024 pixel) LIS: Bi-directional, polling mode, ASTM, ethernet Printouts By patient, single test, complete sample, work sheet, method and QCs, calibration curves, kinetics, continuous printing

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Laboratory Usage

Backed by a team of experienced professionals, we are offering Water & Soil Analysis Kits Digital with 7 Parameters. The given product is available on numerous specifications in promised time-frame as per the customer’s demand. Offered product is manufactured as per industry standard by our workforce at our manufacturing unit using finest material. This product is checked on numerous parameters so as to deliver a flawless range. Features: Precisely designed Easy to use Durability Product Details: Application Laboratory Use Brand Swastik Type Soil Analyzer Kit No of Parameter 7 Display Digital Usage To Analyze Water and Soil

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Hemostasis Analyzer

Product Description: It’s a modern and advanced analyzer in Hemostasis. This single channel coagulation analyzer redefines the benefits in its class Erba. ECL 105 can perform PT, APTT, Fibrinogen, Thrombin Time, All Factiors, Lupus and DDimer. Product Features: Clotting Tests such as PT, aPTT, Fibrinogen, Thrombin time, Factors, Lupus anticoagulant performed using Light scatter principle Tests like D Dimer performed using Immuno-turbidimetry principle Interactive touch screen interface Clotting Graph provides details of the clotting testCuvette 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 105 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 centres It is used in Research Facilities to perform PT and aPTT on animal samples such as rat, mouse, rabbit, hamsters etc Key Specifications: Single channel semi-automated hemostasis system It can analyze 1 test at a time Sample id can be 14 digits alphanumeric, with progressive id or custom id options It is also possible to have a second position of assay preparation/incubation during the analysis of the current one, using preparation line option Optically detects and automatically moves to the next assay steps and auto starts the measurements Tests principles: Clotting (scattered light at 640nm) Immuno-turbidimetric (turbidimetry at 800nm) Dimensions / Weight: Dimension : 216 x 205 x 75 mm Weight : ~1 kg 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 : 150 VA or less Calibrations: Up to 6 calibration levels per assay Storage of the active calibration curve Quality Controls: Up to 12 different control 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 1000 results for QC determinations Up to 1000 results for patients 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 pen drive. Regular backup and file purging is recommended from the USB pen drive to insure rapid operations. USB pen drive, FAT32 formatted

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Clinical Chemistry

Product Description: An advanced & versatile semi automated analyzer for all Clinical chemistry, Electrolytes, Immunoturbidimetric assays and Coagulation test Product Features: Semi automated analyzer 56 direct access keys Temperature selection for 20oC - 40oC in steps of 1oC 5 reporting formats Online display of reaction curve Result recalculation Three levels of quality control with Levy Jennings plot 5 reporting formats USB port interface for PC & printer Product Applications: Entire range of Clinical chemistry, Electrolytes, Immunoturbidimetric assays and Coagulation Optical Module: Static photometer with photometric range (340-670) 8 Interference filters 340, 405, 450, 505, 546, 578, 600 and 670 n.m. Silicon photodiode detectors Photometric range from 0 to 3.0 OD Quartz Halogen lamp of 12V, 20W Measuring Module: Unique Triple cuvette system 18 µl Flow cell 10 mm Square cuvette 6 mm Round glass tube with adaptor Peltier temperature control: 20°C-40°C in steps of 1°C Peristaltic Pump Minimum aspiration volume 200 µl Analysis Modes 1-point linear Rate A non-linear 2-point linear 1-point sample blank linear 1-point non-linear 1-point sample blank non-linear 2-point non-linear Absorbance Rate A linear Coagulation Memory: 200 User defined test programs 1000 test result Reagent Blank 3 Levels of QC Result Recall: Collated Reports by Date, ID, Date & ID Test & Date wise Patient Demographics Built-in QC: Daily and monthly monitoring for 3 Levels Levy-Jenning QC graphs Display: High resolution graphics LCD with backlight. View Area: 120 x 92 mm Keyboard: 41 Multifunction Keys and 6 dynamic keys Printer: In built high resolution graphic thermal printer Interface: USB connectivity to PC Direct printer connectivity through USB port Port for External keyboard Power: External Universal SMPS adapter 18V DC, 70W, 115/230V AC (± 10%), 50/60 Hz Size: (mm): 205 (H) x 450 (W) x 300(D) Weight: Approx. 7 Kgs. Optional Accessories: External 16 Position Dry Block Incubator

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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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Rapid Test

Intended Use Diagnos Dengue card is a rapid solid phase Immuno-chromatographic test for the qualitative 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 for presumptive diagnosis between primary and secondary dengue infection. Salient Features Rapid, visual and qualitative Immunoassay. Differential detection of IgM & IgG Antibodies. Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4). See through device for easy interpretation of results. Unique sample processing method ensures highest accuracy in results. Results with in 20 minutes. Longer shelf life : 30 months at 2-30°C. Convenient pack size : 10 tests Sensitivity-95% and Specificity- 97%. Principle

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Rapid Test

ntended Use The 4th Generation DIAGNOS HCV BI-DOT is a visual, rapid, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C Virus in human serum or plasma. The 4th Generation DIAGNOS HCV BI-DOT has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigens. Salient Features Rapid ,visual 4th generation test. Based on Flow Through Technology. Use of unique combination of Core, NS3, NS4, NS5 antigen. Detects all the subtypes of HCV. Result with in 3 min. Shelf life : 24 months at 2-8°C. Sensitivity- 100 %. Specificity- 99.8 %.

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Rapid Test

Intended Use The 4th Generation HIV TRI-DOT + Ag test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 p24 antigen and HIV-1 & HIV-2 antibodies (IgM,IgG & IgA) in Human Serum or Plasma. The test is a screening test for p24 antigen (HIV-1), anti-HIV-1 & anti-HIV-2 and is for in vitro diagnostic use only. It is intended for screening of blood donors or other individuals at risk for HIV-1 & HIV-2 infection and for clinical diagnostic testing. Salient Features Rapid visual test ,based on enzyme immuno assay & Flow Through Technology. Rapid test for simultaneous and differential detection of p24 Antigen & antibodies for HIV on the same device. Ideal for Blood screening: detects sero-negative HIV Cases. Use of gp-41, C terminus of gp120 for HIV-1 antibodies & gp-36 for HIV -2 antibodies. Detection of Group ‘0’ & subtype ‘C’ of HIV-1, which is most prevalent in India. Unique washing steps for clear Interpretation of Results. Evaluated by National Institute of Biologicals- 100 % Sensitivity & 100 % Specificity. Long Shelf life: 15 months at 2-8° C.

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Instruments

The SV300 is a state-of-the-art ventilator that's simple to configure, easy to operate, and versatile in use. It treats pediatric and adult patients with all acuity levels at ICUs and Intermediate Care. Adaptive With its comprehensive list of standard features, including the latest modes of ventilation, the SV300 is appropriate for all levels of patient acuity and in all care settings, from the patient's bedside to transport to another point of care. Comprehensive Equipped with functions that are usually found on intensive care ventilators, the SV300 comes with extensive ventilation modes and unique features that make it a top level ventilator. p84-s4-1 Volumetric CO₂ measurement p84-s4-2 Weaning indicators p84-s4-3 O₂ Therapy p84-s4-4 Intelli Cycle Thanks to the intuitive UI design of the SV300, each function is in logical order so that clinicians do not need to navigate a complex menu. In addition, both the valves and flow sensor support autoclaving. This safety concept is designed to meet the current clinical trends of protecting patients even under the most demanding conditions.

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