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International standardization and regulations for medical electrical equipment

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dc.contributor.author LOZNEN, Steli
dc.date.accessioned 2019-11-01T11:20:56Z
dc.date.available 2019-11-01T11:20:56Z
dc.date.issued 2014
dc.identifier.citation LOZNEN, Steli. International standardization and regulations for medical electrical equipment. In: Health Technology Management. Book of abstracts: proc. of the 3nd Regional Workshop, April 10-11, 2014. Chişinău, 2014, pp. 15. ISBN 978-9975-45-303-5. en_US
dc.identifier.isbn 978-9975-45-303-5
dc.identifier.uri http://repository.utm.md/handle/5014/5837
dc.description Abstract en_US
dc.description.abstract Medical electrical equipment is highly regulated and held to a higher level of safety than nearly all other types of equipment on the market. This kind of equipment refers to any piece of equipment that runs on electric power, battery or mains (plug-in or permanently connected). Over the last 50 years, medical offices have become increasingly populated with highly complex equipment used to diagnose and treat medical conditions. The complexity of the task of ensuring that this equipment maintains the safety of the patient and the operator has grown as the equipment‘s complexity has grown. en_US
dc.language.iso en en_US
dc.publisher Tehnica UTM en_US
dc.rights Attribution-NonCommercial-NoDerivs 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/us/ *
dc.subject medical electrical equipment en_US
dc.subject health en_US
dc.subject equipment en_US
dc.title International standardization and regulations for medical electrical equipment en_US
dc.type Article en_US


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