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.

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.

Buy AccuTest Syphilis Rapid Card Test (50 Tests) Online from Accurex. This Syphilis test is a special test kit designed to detect Syphilis (Treponema Pallidum- IgA, IgM, IgG) antibodies in serum/plasma. Syphilis is caused by the bacterium Treponema pallidum. There different types of test like VDRL test, RPR test, FTA-ABS, etc. AccuTest Syphilis Test Kit is easy to use at home and gives you 99% accurate result in just 5 -20 minutes, with sensitivity & specificity of 99.67%. Recombinant syphilis antigen (17KDa, 15KDa, 47KDa) is immobilized in the lest line region of the device. AccuTest Syphilis Rapid Test is a special test kit designed to detect Syphilis (Treponema Pallidum- IgA, IgM, IgG) antibodies in serum/plasma. This kit is easy to use at home and gives you 99% accurate result in just 5 -20 minutes, with sensitivity and specificity of 99.67%. 1. AccuTest Syphilis is a chromatographic immunoassay kit for rapid qualitative detection of Treponemal antibodies (IgA, IgM, IgG) generated against Treponema pallidum Antigens (17KDa, 15KDa, 47KDa) in human serum or plasma with high sensitivity and specificity. 2. Results just in 5-20 minutes 3. Accu Test Syphilis exhibits sensitivity and specificity of 99.67%. Features: Based on Chromatographic Immunoassay assay for detection of Treponema pallidum antigens Sample: Human Serum or Plasma 2-3 drops of Serum/Plasma sample required for testing Fast: 1 step method, result in just 5 to 20 minutes Excellent sensitivity and specificity of 99.67% Store unused kit at 2-30C Pack size: 50 T Recombinant syphilis antigen (17KDa, 15KDa, 47KDa) is immobilized in the lest line region of the device. After the specimen is added to the specimen well in the device, it reacts with syphilis antigen coated particles in the test. The mixture migrates chromatographically along the length of the test strip and interacts with the immobilized syphilis antigen. The double antigen test format can detect IgA, IgG & IgM in specimens. If the specimen contains TP antibodies a coloured band will appear in the lest line region indicating a positive result. In the absence of TP antibodies a coloured band will not appear in the region indicating a negative result. To serve as a procedural control, a coloured band will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Based on Chromatographic Immunoassay assay for detection of Treponema pallidum antigens Sample: Human Serum or Plasma 2-3 drops of Serum/Plasma sample required for testing Fast: 1 step method, result in just 5 to 20 minutes Excellent sensitivity and specificity of 99.67% Store unused kit at 2-30C Pack size: 50 T Direction for Use Procedure: 1. Bring the pouch to room temperature before opening to avoid condensation of moisture on the membrane of the device. Also bring the specimen to R.T. prior to testing. 2. Label the device with patient’s identification. 3. Add 2-3 drops (approx. 30 pl) of sample into the sample well of the test device. Avoid overflowing. 4. Wait for 5 – 20 minutes and read the result. It is important that the background is clear beforg the result is read. Note: Do not read the result after 30 minutes since specimen back flow may cause false result. STORAGE, STABILITY & HANDLING 1. The kit should be stored at 2 – 30° C. Do not freeze. 2. Do not use the kit past the expiration date stated on label. 3. Take off the device from the sealed pouch just before use as the device is sensitive to humidity and heat.

Oscar Typhoid IgM / IgG TEST DEVICE is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane for differential detection of IgM and IgG antibodies to Salmonella typhi (S. typhi) in human serum, plasma or whole blood. For professional use only. Sensitivity: 92% for IgM and 93% for IgG Specificity: 99% for IgM and 99% for IgG Pack Size: 50 Tests

HCG MidStream Test is a device for the rapid, qualitative and visual detection of hCG in the human urine. This test can be used by self at home or at clinic. Presence of hCG in urine indicates early stage of pregnancy and allows to consult with the doctor / gynecologist for the management of pregnancy and precautions to be taken during the stage of pregnancy. Sensitivity: 25 mIU HCG / ml Specificity: 99.5% Pack Size: 5 Tests

Malaria Pv/ Pf Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of specific antigens of Plasmodium vivax (Pv) pLDH and Plasmodium falciparum (Pf ) HRP-2, in human whole blood. For professional use only. Relative Sensitivity for Pf HRP II: 98.5% Relative Sensitivity for pv LDH: 100% Relative Specificity for Pf HRP II: 99% Relative Specificity for pv LDH: 99% Pack Size: 50 Tests

Malaria Pan/ Pf Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane for simultaneous and differential detection of Pan (LDH antigens of Plasmodium vivax, Plasmodium falciparum, Plasmodium ovale and Plasmodium malariae) and Plasmodium falciparum HRP-Il, in human whole blood. For professional use only. Relative Sensitivity for pHRP II: 98.5% Relative Sensitivity for pan LDH: 100% Relative Specificity for pHRP II: 99% Relative Specificity for pan LDH: 99% Pack Size: 10 Tests

Malaria Pan/ Pf Antigen Test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of Pan LDH antigens of Plasmodium vivax, Plasmodium falciparum, Plasmodium ovale and Plasmodium malariae and Plasmodium falciparum HRP-II, in human whole blood. For professional use only. Relative Sensitivity for pHRP II: 98.5% Relative Sensitivity for pan LDH: 100% Relative Specificity for pHRP II: 99% Relative Specificity for pan LDH: 99% Pack Size: 50 Tests

The Malaria Antigen test - Pf is an in-vitro diagnostic ready to use test based on the principle of lateral flow chromatographic immunoassay for qualitative detection of histidine rich protein (HRP-II) of Plasmodium falciparum (P.f.) in human whole blood. Relative Sensitivity: 99% Relative Specificity: 98% Pack Size: 50 Tests