A "premium tonometer" typically refers to a high-quality, advanced device used to measure intraocular pressure (IOP) in the eye. Intraocular pressure is the fluid pressure inside the eye, which is an important indicator of eye health and is particularly crucial in conditions such as glaucoma. Premium tonometers often incorporate advanced technology and features to provide accurate and reliable measurements of intraocular pressure. Here are some characteristics commonly associated with premium tonometers: Accuracy: Premium tonometers are designed to provide highly accurate measurements of intraocular pressure. They often use sophisticated sensors and calibration methods to ensure precision. Ease of Use: These tonometers are usually user-friendly, with intuitive interfaces and ergonomic designs. They may feature automated measurement functions to streamline the testing process. Versatility: Premium tonometers may offer versatility in terms of measurement methods. For example, some tonometers use applanation tonometry, where a small probe gently flattens a portion of the cornea to measure pressure, while others may use techniques such as air puff tonometry or rebound tonometry. Data Management: Many premium tonometers include features for storing and managing measurement data. This may include digital storage capabilities, connectivity options for transferring data to electronic medical records systems, or integration with software for analysis and reporting. Quality Construction: Premium tonometers are typically constructed with durable materials and undergo rigorous quality control to ensure reliability and longevity. Calibration: These devices often have built-in calibration systems or mechanisms to maintain accuracy over time. Regular calibration ensures that the measurements remain consistent and reliable. Professional Use: Premium tonometers are commonly used in clinical settings by ophthalmologists, optometrists, and other eye care professionals who require precise intraocular pressure measurements for diagnostic and monitoring purposes.
A "premium tonometer" typically refers to a high-quality, advanced device used to measure intraocular pressure (IOP) in the eye. Intraocular pressure is the fluid pressure inside the eye, which is an important indicator of eye health and is particularly crucial in conditions such as glaucoma. Premium tonometers often incorporate advanced technology and features to provide accurate and reliable measurements of intraocular pressure. Here are some characteristics commonly associated with premium tonometers: Accuracy: Premium tonometers are designed to provide highly accurate measurements of intraocular pressure. They often use sophisticated sensors and calibration methods to ensure precision. Ease of Use: These tonometers are usually user-friendly, with intuitive interfaces and ergonomic designs. They may feature automated measurement functions to streamline the testing process. Versatility: Premium tonometers may offer versatility in terms of measurement methods. For example, some tonometers use applanation tonometry, where a small probe gently flattens a portion of the cornea to measure pressure, while others may use techniques such as air puff tonometry or rebound tonometry. Data Management: Many premium tonometers include features for storing and managing measurement data. This may include digital storage capabilities, connectivity options for transferring data to electronic medical records systems, or integration with software for analysis and reporting. Quality Construction: Premium tonometers are typically constructed with durable materials and undergo rigorous quality control to ensure reliability and longevity. Calibration: These devices often have built-in calibration systems or mechanisms to maintain accuracy over time. Regular calibration ensures that the measurements remain consistent and reliable. Professional Use: Premium tonometers are commonly used in clinical settings by ophthalmologists, optometrists, and other eye care professionals who require precise intraocular pressure measurements for diagnostic and monitoring purposes.
An "ECO tonometer" is a type of tonometer used to measure intraocular pressure (IOP) in the eye. Intraocular pressure is the fluid pressure inside the eye, and it's an important aspect of eye health to monitor, especially in conditions like glaucoma, where elevated intraocular pressure can lead to optic nerve damage and vision loss. The "ECO" in ECO tonometer might stand for "Electronic Contact Ophthalmodynamometer." This type of tonometer typically uses electronic sensors and probes to measure intraocular pressure. Contact Method: ECO tonometers usually involve direct contact with the surface of the eye. The device gently touches the cornea to measure the pressure within the eye. Electronic Sensors: These tonometers utilize electronic sensors to detect changes in pressure. When the probe makes contact with the cornea, it measures the force required to slightly flatten the cornea, providing a measurement of intraocular pressure. Digital Display: ECO tonometers often have a digital display that shows the measured intraocular pressure in millimeters of mercury (mmHg) or another applicable unit. Accuracy and Precision: These tonometers are designed to provide accurate and precise measurements of intraocular pressure, which is essential for monitoring eye health and diagnosing conditions like glaucoma.
WHO Approved, First Response Syphilis Anti-TP Card Test is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative, screening, in vitro diagnostic test for the detection of antibodies of all classes specific to Treponema pallidum in human serum, plasma or Venous or capillary whole blood. Product specifications : 100% - Specificity 100% - Sensitivity Detects antibodies specific to Treponema pallidum Rapid Result time within 20-25 Minutes Storage at 4-30C Specimen Type Whole blood, serum, plasma Shelf Life: 24 Months
HCG Urine Pregnancy Test measures the presence of the pregnancy hormone (HCG) in your urine for the early detection of pregnancy.
STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes. Easy to use, Easy to read and interpret Room temperature storage Performance Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
CTK Biotech's, CE Certified , the OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood. Product Description Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity Differentiates Between Igg And Igm To Determine Stage Of Infection One Step Procedure Minimizes Operator Error Due To Sample Preparation High Level Of Reproducibility Test Kits Can Be Used And Stored In A Wide Range Of Temperatures Product Specification:- Brand Name : CTK Biotech Pkg Qty : 1 Number Of Items : 30 Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)
CE certified, Qualitative detection of troponin in anticoagulated (EDTA or heparin) venous whole blood Reaction time: 15 min. A positive result from a threshold (cut-off) of 100 ng/L Storage at 2 to 8 C Test can be used immediately after removal from the refrigerator Storage for 4 weeks at room temperature (15 to 25 C) Roche TROP T sensitive rapid assay is available in 5 and 10 pack sizes Content: 5 disposable test strips (individually sealed) 5 pipettes (150 L) disposable labels 1 package insert
Abbott BinaxNOW S. pneumoniae Antigen Card provides accurate, rapid identification of S. pneumoniae antigen in patients with pneumococcal pneumonia and pneumococcal meningitis with an easy-to-use technology, aiding physicians in providing rapid, focused therapy. Time to Result: 15 minutes Performance data: Urine Sensitivity/Specificity 86% / 94% CSF Sensitivity/Specificity 97% / 99% Ordering Information Cat No. Description Specimen Pack size 710000 Streptococcus Urine, CSF 22 Tests Pneumoniae Ag card
Cat No. 7D2543. By detecting early markers of Hepatitis B infection, the Alere Determineâ?¢ HBsAg helps to diagnose acute infection and confirm chronic infection - allowing healthcare professionals to initiate prompt and appropriate follow-up action for infected patients. Rapid in-vitro qualitative ICT for detection of HBsAg Sample Type: Serum/Plasma/Whole Blood Sample Volume: 50�µL Early marker of infection- helps in diagnosis Facilitates appropriate follow-up of infected patients Collection can be done by fingerprick or venipuncture Clear, dependable results in 15 minutes Quick Reference Card for the detection of HBsAg in human serum/plasma or whole blood.
Cat. No: 03FK10CE. Sd bioline hiv 1/2 pack size: 1 x 30 test one step rapid immunochromatrographic test for the detection of anti - hiv 1/2 in human serum, plasma or whole blood
CAT No : 11621947196. Qualitative detection of troponin in anticoagulated (EDTA or heparin) venous whole blood Reaction time: 15 min. Positive result from a threshold (cut-off) of 100 ng/L Storage at 2 to 8C Test can be used immediately after removal from the Refrigerator Storage for 4 weeks at room temperature (15 to 25 C) Roche TROP T sensitive rapid assay is available in 5 and 10-pack sizes Content: 5 disposable test strips (individually sealed) 5 pipettes (150L) Disposable labels 1 package insert
Cat No : 05FK80I40. The SD BIOLINE Malaria Ag P.f/Pv test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood. Specomen: Whole blood Time to result: 15 -30 minutes Storage: 1-40 degree C for 24 months Performance: Sensitivity: Pf-99.7%, Pv-95.5% Specificity: 99.5 % Optimal screening test for Plasmodium falciparum and Plasmodium vivax.
CAT No : 7D2343. A rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2) Clear, dependable results in 15 minutes Requires minimal training and no equipment So easy it can be used at the lowest levels of health care service Can use whole blood or serum/plasma Collection can be by fingerstick or venipuncture No refrigeration required Storage conditions 2-30C
Cat. No : 11FK45. SD BIOLINE Dengue Duo (Dengue NS1 Ag + IgG/IgM) The SD BIOLINE Dengue Duo kit is a rapid, an in-vitro immunochromatographic, one step assay designed to detect both dengue virus NS1 antigen and antibodies to Dengue virus (Dengue IgG/IgM) in human serum, plasma or whole blood. SD BIOLINE Dengue Duo rapid test contains two test devices (left side ; Dengue NS1 Ag test, right side ; Dengue IgG/IgM test). The SD BIOLINE Dengue Duo kit is intended only for an initial screening test and reactive samples should be confirmed by a supplemental assay such as RT-PCR, IgM / IgG ELISA or HI (Hemagglutination inhibition) test. Detect Dengue Ag and Ab simultaneously at once. Cover acute to convalescence stage Performance: Sensitivity : 92.4% (Dengue NS1 Ag), 94.2% (Dengue IgG/IgM) Specificity : 98.4%(Dengue NS1 Ag), 96.4% (Dengue IgG/IgM) In primary infection with the dengue virus, IgG antibody appears a few days after IgM. In primary infections, IgG antibodies are produced at a lower level compared to IgM but will persist for many years after infection. In secondary infections, IgG response may rise quickly before or simultaneously with an IgM response and will become the predominant immunoglobulin isotype in secondary infections.
Cat No. 08FK50. SD BIOLINE TB Ag MPT64 Rapid is a rapid immune chromatographic identification test for the M. tuberculosis complex. M. tuberculosis has been known to secrete more than 33 different proteins. One of the predominant proteins, MPT64 was found in the culture fluid of only strains of the M. tuberculosis complex. Rapid discrimination between the M. tuberculosis complex and MOTT bacilli Identification of the M. tuberculosis complex in combination with culture systems Sample: Colony, Condensation fluid(Solid cultures) or Liquid cultures Interpretation time: 15minutes Detection limit: 105CFU/ml.
Cat No.02FK10I30. SD BIOLINE HCV test is an immunochromatographic rapid visual test for the qualitative detection of antibodies specific to HCV in human serum, plasma or whole blood Immobilized material: Recombinant HCV Core, NS3, NS4, NS5 Ag Specimen Type: Serum, Plasma, Whole blood Sample Volume: 10MuL Shelf Life: 24months Storage: 2-30oC Performance: Sensitivity: 99.5% and Specificity: 98% One Step Hepatitis C Virus Test.
The Alere SD BIOLINE Malaria Ag P.f/Pan test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and common Plasmodium lactate dehydrogenase (pLDH) of Plasmodium species in human whole blood. Optimal screening test for P.falciparum and other Plasmodium species Ordering Information Cat No. Description Type Pack size 05FK63I01 SD Malaria Device 1 Test
CAT No : RK026-30. STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes. Easy to use, Easy to read and interpret Room temperature storage Performance Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
CAT No : RK025-40. One step, rapid immunothematographic test for the differential detection between Plasmodium falciparum Histidine- Rich Protein II (HRP II) and Plasmodium species (P. falciparum , P vivax P. ovale, P. malariae) lactate dehydrogenase (pLDH) in human whole blood Kit Contents: Standard Q Malaria Pf/PV Ag cassette x 40 Specimen transfer device 3 microlitre x 40 Butter bottle 3m1 x 02 Instructions for use x 01 STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and CAT Cat.No : RK025-40. Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity Advantage: Distinguish the infection between P.falciparum and P.vivax Optimized on-site diagnosis with the small diagnostic kit Able to read positive/negative infections fast and accurately with a little blood (5�µl) Room temperature storage.
