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Medical Device Directive

См. также в других словарях:

  • Medical Device Directive — Die Richtlinie 93/42/EWG des Rates vom 14. Juni 1993 über Medizinprodukte ist eine EG Richtlinie und wird in Deutschland und Österreich kurz als Medizinprodukterichtlinie bezeichnet. International spricht man von der Richtlinie als Medical Device …   Deutsch Wikipedia

  • Medical Devices Directive — European Union directive: Directive 93/42/EEC Council Directive concerning medical devices Made by Council Made under Art. 100a TEEC …   Wikipedia

  • Medical device — A medical device is a product which is used for medical purposes in patients, in diagnosis, therapy or surgery[citation needed]. Whereas medicinal products (also called pharmaceuticals) achieve their principal action by pharmacological, metabolic …   Wikipedia

  • Medical software — Logo, by Harry Gouvas In computers, medical software is a significant branch of software engineering. Many medical devices that monitor or control patients are predominantly controlled by software. Medical devices are frequently regulated and… …   Wikipedia

  • Italian Device Registration — The Italian Ministry of Health (MOH) has implemented mandatory procedures for the Italian Registration of Medical Devices as of May 1st, 2007. Overview Placing a Medical Device into the European market is contingent upon compliance with the… …   Wikipedia

  • Restriction of Hazardous Substances Directive — European Union directive: Directive 2002/95/EC Directive on the restriction of the use of certain hazardous substances in electrical and electronic equipment Made by Council Parliament …   Wikipedia

  • Combat Medical Badge — Awarded by United States Army Type Badge …   Wikipedia

  • Prime Directive — This article is about the guiding principle in the fictional Star Trek universe. For other uses of Prime Directive, see Prime Directive (disambiguation). In the universe of Star Trek, the Prime Directive, Starfleet s General Order #1, is the most …   Wikipedia

  • European Authorized Representative — A European Authorized Representative (E.A.R.) serves as a legal entity designated by non European Union (EU) manufacturers, to represent them in the EU and ensure their compliance with the European Directives. Overview Regulation of goods… …   Wikipedia

  • MDD — Major Depressive Disorder (Medical » Physiology) * Medical Device Directive (Medical » Hospitals) * Medical Devices Directive (Governmental » US Government) * McDonnell Douglas (Business » Firms) * Mirrored Drive Door (Computing » Hardware) *… …   Abbreviations dictionary

  • Europäische Medizinprodukterichtlinie — Die Richtlinie 93/42/EWG des Rates vom 14. Juni 1993 über Medizinprodukte ist eine EG Richtlinie und wird in Deutschland und Österreich kurz als Medizinprodukterichtlinie bezeichnet. International spricht man von der Richtlinie als Medical Device …   Deutsch Wikipedia

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