Urodynamic Measuring System

8''All Infrared Detection Body Temperature Intelligent Fast Face Recognition Android all-in-one machine Suitable for scenic spot,office,hotel,school,shopping mall,community or any other places require auto face recognition.

7ich screen 4gb capacity core 200w piexl camera

The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip. The system is intended to be used by a single patient and should not be shared. The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is intended for self-testing outside the body (in vitro diagnostic use) by people with diabetes at home and with their healthcare professionals in a clinical setting as an aid to monitor the effectiveness of diabetes control. The OneTouch® Selectâ?¢ Plus Blood Glucose Monitoring System is not to be used for the diagnosis of or screening of diabetes or for neonatal use. The system is intended to be used by a single patient and should not be shared. Test Principle Glucose in the blood sample mixes with the enzyme Glucose Oxidase (see page 130) in the test strip and a small electric current is produced. The strength of this current changes with the amount of glucose in the blood sample. Your meter measures the current, calculates your blood glucose level, displays the blood glucose result, and stores it in its memory. Use only OneTouch® Selectâ?¢ Plus Control Solutions and Test Strips with the OneTouch® Selectâ?¢ Plus Meter.

Product description Partial discharge inspection instrument is a digital partial discharge charged detection instrument designed by our company based on years of experience in partial discharge measurement. It adopts two emerging technologies, ultra high frequency (UHF) measurement and ultrasonic (US) measurement. This system uses modern electronic and computer integrated technology to realize signal amplification, filtering, data acquisition, data processing, partial discharge parameter calculation, map drawing, and automatic generation of test reports, thereby completing the intelligent measurement and analysis of partial discharge. This device adopts handheld design and Wince system development; the device is lightweight, convenient to carry, fast to measure, and easy to use on the spot; it has friendly interface, simple operation, and high refresh rate; and the device has complete functions, strong anti-interference ability, and accurate measurement. This instrument has no damage to the power equipment to be tested during the testing process, and has no impact on the operation of the equipment. According to the maps obtained by the multiple detection modes of the UHF and US methods, the diagnostic analysis of the detection of insulation defects or hidden dangers of power equipment can be performed to clearly determine the operating status of the power equipment. Technical index Host parameters Number of interfaces 2 interfaces 1 UHF interface 1 US interface Sampling accuracy 12bit Way of synchronization Internal synchronization,External synchronization, Light synchronization UHF parameters Measurement frequency range 300MHz-1.5GHz Output method Output with SMA head Receiving method Receive with antenna Transfer method Coaxial cable Sensitivity 70dB Mean sensitivity 50dB Dynamic Range 80dB Hardware Display screen 4.3 TFT true color LCD screen Resolution 480 272

The Herpes Simplex Virus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of IgG antibodies to Herpes Simplex Virus (HSV) in human serum/plasma samples. HSV-1 is usually associated with infection in oropharyngeal area and eyes, while HSV-2 causes mostly genital and neonatal infections (5, 6), however, the tissue specificity is not absolute (7). HSV-2 can be isolated occasionally from the oropharynx and 5-10% of primary genital infections may be caused by HSV-1. Infants infected with HSV appear normal at birth, but almost invariably develop symptoms during the newborn period (5, 8, 9). Neonatal HSV infection may remain localized or become disseminated. Localized infection may involve one or a combination of sites. These are skin, eyes, mouth or the central nervous system. Disseminated infection is manifested by pneumonitis, hepatitis, disseminated intravascular coagulopathy and encephalitis. Of the infants with neonatal HSV, about one half of those surviving will develop severe neurological or ocular sequelae. A number of serological procedures have been developed to detect antibodies to HSV. These include complement fixation, indirect immunofluorescent antibody, plaque neutralization, and ELISA (6, 8, 10). Antibody of the IgG class is produced during the first 2-3 weeks of infection with HSV and exists only transiently in most patients. Serologic procedures, which measure the presence of IgG antibodies, help discriminate between primary and recurrent infections, since IgG antibodies is rarely found in recurrent infections. High affinity IgG antibodies to HSV, if present in a sample, may interfere with the detection of IgG specific antibody (9). High affinity IgG antibody may preferentially bind to HSV-1 antigen leading to false negative IgG results. Also, rheumatoid factor, if present, along with antigen specific IgG, may bind to IgG causing false positive IgG results. Both problems can be eliminated by deactivating IgG in the sample before testing for IgG.

Supplier: Covid 19 antigen rapid test kit, antibody test, antigen test, poct, point of care testing, hba1c, bgms for human and pets, blood glucose monitoring system, diagnostic reagents, diagnostic instruments, medical devices, glucose, lipid(tc, tg, hdl, cal ldl) monitoring system, hemoglobin measuring system

The GENEDIA W COVID-19 Ag is an in vitro diagnostic single-use test and qualitative immunoassay to detect SARS-CoV-2 antigen in nasopharyngeal swab and sputum specimen from human. This assay is designed for professional personnel in laboratory and at point-of-care as an aid in screening patients suspected of being infected and asymptomatic patients. Allow wider testing with fast test time (10 minutes) Clinically proven data of asymptomatic patients available Separately packed extraction solution to minimize the possibility of contamination No additional instruments required Package Unit : 20 Tests/Kit Expiration Date : 24 Months (while sealed in the original aluminum foil pouch) GCMS manufactures COVID-19 antigen test kit, the GENEDIA W COVID-19 Ag which is listed on the EU common list, also with GMP and ISO certifications. GENEDIA W COVID-19 Ag is unaffected based on the in-silicon analysis of the mutations in the nucleocapsid (N gene) of Omicron viruses. Letter of statement is available upon your request. To get over COVID-19 pandemic, especially the recent Omicron breakout, currently we are doing big promotions for three kinds of COVID-19 Ag kit. All are in stock and available right away. 1. Nasopharyngeal 2. Nasal 3. Saliva The price is negotiable according to the amount of your order and shipping term. No MOQ is required but we prefer 1 pallet with 9,600 tests. (20 tests/kit, 30 kits/carton, 16 cartons/pallet)