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Medical halogen penlight: to see into the eye, natural orifices, etc. and to test for pupillary light reflex, etc. Medical ultrasound: to create an image of internal body structures Nasogastric tube: for nasogastric suction or the introduction of food or drugs into the body Nebulizer: to produce aerosols of drugs to be administered by ...
A medical device is an instrument, apparatus, implant, in vitro reagent, or similar or related article that is used to diagnose, prevent, or treat disease or other conditions, and does not achieve its purposes through chemical action within or on the body (which would make it a drug).
A portable drug-delivery device, comprising an insulin container (prefilled for disposable pens, or refillable with cartridges); a dialing system to select the dose (in increments of 0.5 or 1 Unit); and a button which delivers the drug when pressed; disposable needles are attached prior to each use. To administrate insulin under the skin. [10]
I. Ice pack; Impedance cardiography; Inadine; Incentive spirometer; Incubator (culture) Inhaler spacer; Injector pen; Instruments used in cardiology; Instruments used in dermatology
Many drugs have more than one name and, therefore, the same drug may be listed more than once. Brand names and generic names are differentiated by capitalizing brand names. See also the list of the top 100 bestselling branded drugs , ranked by sales.
used for puncturing into the spine (or cisterns or fontanelles of a new born) for cerebro-spinal fluid aspiration or for injection drugs, specially anesthetics in spinal blocks, epidurals, etc. Ryle's tube or Nasogastric tube: used for nasogastric suction of ingested toxins (or at times introduction of food or drugs). video link
Drug delivery devices are specialized tools for the delivery of a drug or therapeutic agent via a specific route of administration. Such devices are used as part of one or more medical treatments . Contents
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as the directives 93/42/EEC on medical devices and 90/385/EEC on active implantable medical devices have been fully repealed on 26 May 2021 by Regulation (EU) no. 2017/745 (MDR); furthermore, Brexit triggers updates in these sections (U.K. developed their own ...
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