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XT Anesthesia Workstation, an automated dispensing cabinet used in hospital operating rooms. Automated dispensing is a pharmacy practice in which a device dispenses medications and fills prescriptions. ADCs, which can handle many different medications, are available from a number of manufacturers such as BD, ARxIUM, and Omnicell.
The central sterile services department (CSSD), also called sterile processing department (SPD), sterile processing, central supply department (CSD), or central supply, is an integrated place in hospitals and other health care facilities that performs sterilization and other actions on medical devices, equipment and consumables; for subsequent ...
A hybrid operating room is an advanced surgical theatre that is equipped with advanced medical imaging devices such as fixed C-arms, X-ray tomography (CT) scanners, or magnetic resonance imaging (MRI) scanners. [1] These imaging devices enable minimally-invasive surgery.
For example, sterile equipment and fluids are used during invasive medical and nursing procedures. [11] The largest manifestation of such aseptic techniques is in hospital operating theaters, where the aim is to keep patients free from hospital micro-organisms. [12] Packaged, sterilized surgical instruments
Suction device: to suck up blood or secretions Surgical scissors: used for dissecting or cutting Thermometer: to record body temperature: Tongue depressor: for use in oral examination Transfusion kit: to transfuse blood and blood products Tuning fork: to test for deafness and to categorize it Ventilator
Medical nursing homes, including residential treatment centers and geriatric care facilities, are health care institutions which have accommodation facilities and which engage in providing short-term or long-term medical treatment of a general or specialized nature not performed by hospitals to inpatients with any of a wide variety of medical ...
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as the directives 93/42/EEC on medical devices and 90/385/EEC on active implantable medical devices have been fully repealed on 26 May 2021 by Regulation (EU) no. 2017/745 (MDR); furthermore, Brexit triggers updates in these sections (U.K. developed their own ...
The U.S. congressional review concluded medical devices would require actual device experience in a clinical setting and sufficient reporting of adverse data events. The legislation would encompass medical devices demonstrating the potential for life-threatening events and accurate adverse data collection would be required for informed ...