International standardization and regulations for medical electrical equipment

LOZNEN, Steli

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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