TACHOMETER/STROBOSCOPE, Model : BP-2259 ( 2 in 1, DIGITAL PHOTO TACHOMETER with DIGITAL STROBOSCOPE ) FEATURES* Intelligent, microprocessor circuit design, high accuracy, wide range, digital readout.* One instrument include two functions of " Digital Photo Tachometer " & " Digital Stroboscope "* Digital Stroboscope :Wide setting range from 100 RPM to 100,000 RPM, digital display with high accuracy. Modern solid state high visible orange light, long life, almost maintenance free. It is ideal for inspectingand measuring the speed of moving gears, fans, centrifuges, pumps, motors and other equipment used in general industrial maintenance, production, quality control, laboratories and as well as for schools and colleges for demonstrating strobe action.* Digital Photo Tachometer :No contact RPM measurement, wide measuring range from 0.5 to 100,000 RPM. 0.1 RPM resolution for the measured value < 1000 RPM. The last value, max., value, min. value can be stored into the memory automatically & be obtained by pressing " Memory Call Button ". High visible LCD display gives RPM reading exactly with no guessing or errors.* The use of durable, long lasting components, including a strong, light weight ABS plastic housing.Cabinet has been carefully shaped to fit comfortable in either hand. GENERAL SPECIFICATIONS Display 5 digits, 10 mm ( 0.4" ) LCD Operation 0 - 50 (32 - 122 ). ( Liquid Crystal display ) with Temperature function annunciation. Operating Less than 80% RH.Accuracy ± ( 0.1 % + 2 digit ). Humidity Sampling Time 1 second ( 60 RPM ). Size 215 x 65 x 38 mm.Time base:Quartz crystal. (8.5 x 2.6 x 1.5 inch). Circuit Exclusive one-chip design Weight 300g(0.66 LB)/including battery.microprocessor LSI circuit. Accessories : Carrying case ................... 1 PC.Battery 4 x 1.5V AA ( UM-3 ) battery. Operation manual ..............1 PC.ELECTRICAL SPECIFICATIONS ( PHOTO TACHOMETER )Measurement Range 5 to 99,999 RPM Resolution 0.1 RPM ( < 1,000 RPM ) 1 RPM ( 1,000 RPM )Photo Tach. detecting distance 50 to 150 mm/2 to 6 inch. * Typical max. 300 mm/12 inch depending upon ambient light.ELECTRICAL SPECIFICATIONS ( STROBOSCOPE )Stroboscopic 100 to 100,000 FPM/RPM Flash tube High efficiency orange LED Flash Rate FPM: flash per minute lamp.RPM : round per minute Flash Duration Approximately 60 to 1,000Flash Adjust 3 ranges : microseconds. Range Range A: 100-1,000 FPM Flash color Orange Range B: 1,000-10,000 FPM Flash Duration Approx. 16% of period time. Range C: 10,000-100,000 FPM Flash Adjust Coarse adjust knob and Resolution 0.1 FPM/RPM. Knob Fine adjust knob.(Less than 1,000 FPM/RPM) Calibration Crystal time base and1 FPM/RPM microprocessor circuit, don't(Over 1,000 FPM/RPM) necessary take any external calibration process. OPERATIONS PROCEDURES ( STROBOSCOPE )Preparation Determine the range switch to " 1000 RPM " ," 10,000 RPM " or" 100,000 RPM " position.Checking When checking speed, care must be taken to insure that the strobe is flashing in Speed unison (one to one) with the object being monitored. A Stroboscope will also stop motion at 2:1, 3:1, 4:1 et., this is normally referred to as harmonies. To be sure of unison, turn the dial until two images appear - this will double the actual speed. Then lower the flashing rate until a single and stationary image appears -this is the actual true speed.Checking For motion analysis, simply locate the actual speed as mentioned above and then Motion turn the dial slowly up or down. This will give a slow motion effect allowing complete inspection.

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 Diagnos Celiac Card is a visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of anti tTG IgA, IgG & IgM antibodies in Human Serum or Plasma. The assay is intended to be used as an aid in the recognition and diagnosis of Celiac disease. Salient Features Rapid, Visual and Qualitative Antibody Test. Excellent Sensitivity: 99.26% & Specificity: 99.50%. Results within 20 minutes. Long Shelf life 24 months at 2-8°C. Bio-hazard free, fully covered, see-through Device. No instrument required.

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 %.

Intended Use Advantage Leptospira IgM & IgG card is visual, rapid, sensitive and qualitative immunoassay for the detection of Leptospira specific IgM & IgG antibodies in human serum or plasma. Salient Features Rapid qualitative test for differential detection of Leptospira specific IgM and IgG Antibodies in Human serum/plasma. One step test procedure, add sample & read results Infection free see through device. Results with in 20 minutes. Shelf life of 30 months at 2-30°C. Excellent Sensitivity- 99 % and Excellent Specificity- 99.5%

Intended Use Advantage Malaria PAN+Pf Card is a rapid, visual and sensitive immunoassay for the qualitative diagnosis of infection with P.falciparum and other Plasmodium species (P.falciparum/P.vivax/P.malariae/P.ovale) in human whole blood only. Salient Features Detects P.f. (HRP-2) and PAN(pLDH) Individually pouched Single tests- Practical & Safe Infection free- See through Device Easy to perform test Easy to interpret Colour bands Results within 20 minutes Sensitivity of 100% & Specificity of 99.80% Longer shelf life -30 months, storage at 4-30° C

A high-end ventilator featured with 1080P HD wide screen, combines an intuitive customized UI with powerful assistive tools and modules. Operate with Ease In the modern busy clinical environment, ease of use is a fundamental requirement for all medical devices. With this in mind, the new SV800/SV600 ventilators enable clinicians to set and deliver ventilation therapies quickly and easily via the intelligent ergonomic design and flat user interface. Intelligent Decision Making Ventilation modes and decision-supporting tools like SBT are developed on the basis of clinical needs and professional guidelines to help free up medical personnel’s time on device operation and focus more on their patients. p68-s4 Extensive ventilation therapy and decision support tools Smart ventilation solution: AMV TM + IntelliCycle TM Emergency solution: CPRV TM Sequential treatment regimen: Non-invasive ventilation & high flow oxygen therapy Dual channel auxiliary pressure measurements Lung protection kit Expandable Capabilities Securing your devices future is reliant on being able to expand your devices capabilities by interacting or integrating new features and technologies. The SV800/SV600 ventilators allow just this. Thanks to latest software and platform it is utilizing, your device is ready to embrace new technological advancement with ease. p68-s0-0 Integrated neonatal module with tidal volume setting down to 2ml Plug & Play modules , including SpO₂, mainstream or sidestream CO₂ Backup air supply in case of central air supply failure and during intra-hospital transport Seamlessly connected to the hospitals clinical information system via the Mindray BeneLink and eGateway modules, or directly via the HL7 p68-s5 Brand - Mindray Model Name/Number SV800 Patient Age Group Adult, Pediatrics & Neonatal Tidal Volume For adult : 100 to 4000 ml, For Pediatric 20 to 300 ml, For neonatal : 2 to 100 ml Ventilation Mode V-A/C, P-A/C, V-SIMV,P-SIMV, Duolevel, CPAP, PSV, APRV, PRVC, NIV, PRVC-SIMV, AMV, CPRV, PSV-S/T, nCPAP, VS Respiratory Rate For adult/pediactrics : 1 to 100/min,for neonate :-1 to 150/min Additional Details Weight 45 kg ventilator + 16.3 kg trolley Plateu (%) OFF, 5% to 60% Peak airway pressure 0 to 100 cm H2O SIMV Rate ,Cycle/min 1 to 60 rpm Mounting type Trolley I:E Ratio 1:10 to 4:1 Touch screen 18.5 inch color active matrix TFT touch screen RSBI 0-9999/1/(L-min) Features Customizing the UI Graphic guidelines Single level menu design Dual channel auxiliary pressure monitore

The OnSite Troponin I Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of cardiac Troponin I (cTnI) in human serum, plasma or whole blood at a level equal to or higher than 1 ng/mL. It can be performed within 15 minutes by minimally skilled personnel, and without the use of laboratory equipment. The OnSite Troponin I Combo Rapid Test is intended to be used by healthcare professionals as an aid in the diagnosis of acute myocardial infarction (AMI). Any use or interpretation of this preliminary test result must also rely on patient’s symptoms and the professional judgment of a physician. A more precise test method such as an instrument method must be used to confirm the test result obtained by this device. Normally the level of cTnI in the blood is very low. cTnI is released into the blood stream in forms of free cTnI and cTnI-C-T complex at 4-6 hours after myocardial cell damage. The elevated level of cTnI could be as high as 50 ng/mL during 60-80 hours after AMI and remains detectable for up to 10-14 days post AMI. Therefore, circulating cTnI is a specific and sensitive marker for AMI. Clinical performance: Relative Sensitivity: 95.8% (95% CI: 91.5-97.9%) compared to a reference CLIA Relative Specificity: 99.7% (95% CI: 98.8-99.9%) Analytical sensitivity: The detection limit of cTnI is 1.0 ng/mL or greater in serum, plasma or whole blood specimen Cross-reactivity: No cross reactivity with 10 µg/mL skeletal muscle TnI, 2,000 ng/mL cardiac muscle TnT, 20 µg/mL cardiac muscle Myosin Dose hook effect: No hook effect was observed for cTnI at concentrations up to 3,521 µg/mL Interference: No interference was seen with 20 mg/dl Acetaminophen, 20 mg/dl Acetylsalicylic acid, 10.5 g/dl Albumin, 20 mg/dl Ascorbic acid, 1,000 mg/dl Bilirubin, 20 mg/dl Caffeine, 800 mg/dl Cholesterol, 200 mg/dl Creatinine, 20 mg/dl Gentistic acid, 1,000 mg/dl Hemoglobin, 600 mg/dl Oxilic acid, 1,600 mg/dl Triglycerides Shelf life: 24 months Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample diluent (REF SB-R3002, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Insert MedlinePlus: Troponin Test Poster

The OnSite hCG Combo Rapid Test is a lateral flow chromatographic immunoassay for the early detection of pregnancy, by providing a quick direct visual test for the placental hormone, hCG in human serum, plasma and urine. It can be performed within 5-10 minutes by minimally skilled personnel, and without the use of laboratory equipment. The OnSite hCG Combo Rapid Test is not intended for quantitative results, nor for over the counter (OTC) sales. It is intended to meet all requirements for yielding rapid, easily read, qualitative results for the purpose of early pregnancy detection via assay of hCG, a placental hormone that may be present in human serum, plasma or urine. The hCG detection limit the OnSite hCG Combo Rapid Test is 12.5 mIU/mL in serum or plasma specimen, and 25 mIU/mL in urine specimen. It is designed for professional use only, and provides only preliminary analytical data. For a final diagnosis of pregnancy, a more specific alternative clinical method must be used to obtain a confirmed analytical result. Clinical accuracy: In comparison with a reference chemiluminecsence or ELISA, hCG detection is 100% sensitivity and 100% specificity in urine specimens 100% sensitivity and 99.5% specificity in serum specimens Analytical sensitivity: 100% positive detection rate at 12.5 mIU/mL in serum/plasma specimens and 100% positive detection rate at 25 mIU/mL in urine specimens Analytical specificity: no cross reactivity with 1,000 mIU/mL human luteinizing hormone (hLH), 1,000 mIU/mL human follicle stimulating hormone (hFSH), and 1,000 mIU/mL human thyroid stimulating hormone (hTSH) Dose hook effect: no dose hook effect was observed for hCG at concentrations up to 500,000 mIU/mL in urine specimens Interference: No interference was seen with 35 biological and chemical analytes commonly found in OTC, prescriptions or abuse drugs in urine or serum/plasma specimens, as well as pH 4-9 (see detail in the package insert) Shelf life: 24 month Kit box package: 1. Individually sealed foil pouches containing; a. One dip strip device b. One desiccant 2. One package insert (instruction for use) Tube package: 1. Strip Package 2. One desiccant 3. One package insert (instruction for use) CTK Products at a Glance Drugs.com: Overview of Human Chorionic Gonadotropin Inserts