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in microscopy, serology, etc. as the solid backing on which test samples are Petri dish: used for preparation of culture media and the culture of organisms they are in Glass beaker: reagent storage Glass flask: gastric acid, or other fluid titration: Pasteur pipette: for aspiration and addition of reagents Graduated pipettes
Infection control equipment: as in gloves, gowns, bonnets, shoe covers, face shields, goggles, and surgical masks for preventing nosocomial or healthcare-associated infection: Instrument sterilizer: to sterilize instruments in absence of an autoclave: Kidney dish: as a tray for instruments, gauze, tissue, etc. Measuring tape
Clinical laboratory in a hospital setting showing several automated analysers.. A medical laboratory or clinical laboratory is a laboratory where tests are conducted out on clinical specimens to obtain information about the health of a patient to aid in diagnosis, treatment, and prevention of disease. [1]
In medicine, sampling is gathering of matter from the body to aid in the process of a medical diagnosis and/or evaluation of an indication for treatment, further medical tests or other procedures. In this sense, the sample is the gathered matter, and the sampling tool or sampler is the person or material to collect the sample.
Barcode technology is ideally suited for tasks in which a human being is stationary and objects are moving (e.g. blood sample collection and labeling). Barcoding technology in healthcare will eventually begin to shift over to the use of 2-D symbologies to accommodate size restrictions and the growing need for large amounts of data.
Variety of microbiological samples. A laboratory specimen is sometimes a biological specimen of a medical patient's tissue, fluids, or other samples used for laboratory analysis to assist in differential diagnosis or staging of a disease process. These specimens are often the most reliable method of diagnosis, depending on the ailment.
This article needs to be updated.The reason given is: the section related to E.U. needs further updates (esp. in sections 3.2 and 4.2.2) as the directives 93/42/EEC on medical devices and 90/385/EEC on active implantable medical devices have been fully repealed on 26 May 2021 by Regulation (EU) no. 2017/745 (MDR); furthermore, Brexit triggers updates in these sections (U.K. developed their own ...
Every medical treatment facility should have policies and processes on equipment control and asset management. Equipment control and asset management involves the management of medical devices within a facility and may be supported by automated information systems (e.g., enterprise resource planning (ERP) systems are often found in U.S. hospitals, and the U.S. military health system uses an ...
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