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VE: vaginal examination (manual examination) VEB: ventricular ectopic beat: VED: Vacuum Erection Device VEE: Venezuelan equine encephalitis: VF V-fib: ventricular fibrillation: VFSS: videofluoroscopic swallow study: VH: visual hallucinations vaginal hysterectomy VHL: Von Hippel–Lindau disease: VIN: vulvar intraepithelial neoplasia VIR ...
The main discussion of these abbreviations in the context of drug prescriptions and other medical prescriptions is at List of abbreviations used in medical prescriptions. Some of these abbreviations are best not used, as marked and explained here.
Global Medical Device Nomenclature (GMDN) is a system of internationally agreed generic descriptors used to identify all medical device products. This nomenclature is a naming system for products which include those used for the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.
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).
Embotrap III Revascularization Device [7] Embovac Aspiration Catheter [8] Cerenovus Large Bore Catheter [9] Cerenovus Nimbus [10] Cerebase DA Guide Sheath [11] Trufill n-BCA Liquid Embolic System [12] Orthopedics (DePuy Synthes) Velys Digital Surgery platform [13] Attune Cementless Fixed Bearing Knee [14] Actis Hip Stem [15] Inhance Shoulder ...
cite journal}}: CS1 maint: multiple names: authors list : Auvard's speculum: Alfred Auvard: Gynaecology: vaginal speculum [4] Luer taper, Luer lock: Hermann Wülfing Luer: General use: Fitting to ensure leak-free connection in medical fluid administration systems [5] Penrose drain: Charles Bingham Penrose: Surgery
Medical devices first came under comprehensive regulation with the passage of the Federal Food, Drug, and Cosmetic Act of 1938 (FD&C), [9] which replaced the earlier Pure Food and Drug Act of 1906. The FD&C allowed the FDA to perform factory inspections and prohibited misbranded marketing of cosmetic and therapeutic medical devices. [10]
Pronunciation follows convention outside the medical field, in which acronyms are generally pronounced as if they were a word (JAMA, SIDS), initialisms are generally pronounced as individual letters (DNA, SSRI), and abbreviations generally use the expansion (soln. = "solution", sup. = "superior").
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