Search results
Results from the WOW.Com Content Network
General use: Fitting to ensure leak-free connection in medical fluid administration systems [5] Penrose drain: Charles Bingham Penrose: Surgery: Tube allowing for postoperative drainage from surgical sites
A medical device hijack (also called medjack) is a type of cyber attack. The weakness they target are the medical devices of a hospital. This was covered extensively ...
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 medical device is any device intended to be used for medical purposes. Significant potential for hazards are inherent when using a device for medical purposes and thus medical devices must be proved safe and effective with reasonable assurance before regulating governments allow marketing of the device in their country.
Uses; Bandage: material used to support a medical dressing or injured body part Bedpan: for patients who are unconscious or too weak to sit up or walk to the toilet to defecate: Cannula: to create a permanent pathway to a vein (or artery) for the purpose of repeated injections or infusion of intravenous fluids: Catheter
A major branch is medical biostatistics, which is exclusively concerned with medicine and health. [66] Bipolar disorder – is a mental disorder that causes periods of depression and periods of abnormally elevated mood [67] [68] [69] Birth control – also known as contraception and fertility control, is a method or device used to prevent ...
Single-use medical devices include any medical equipment, instrument or apparatus having the ability to only be used once in a hospital or clinic and then disposed. The Food and Drug Administration defines this as any device entitled by its manufacturer that it is intended use is for one single patient and one procedure only. [ 1 ]
The practice of reusing medical devices labeled for only one use began in hospitals in the late 1970s. [8] After a thorough review by the U.S. FDA in 1999 and 2000, [8] the agency released a guidance document for reprocessed SUDs that began regulating the sale of these reprocessed devices on the market, [9] under the condition that third-party reprocessors would be treated as the manufacturer ...