Resumen
This document provides guidance on the maintenance management of medical devices that are under the supervision of healthcare delivery organizations.
This document is not applicable to:
a) modification, refurbishment or remanufacturing of medical devices;
b) manufacturers that are responsible for installation, testing, maintenance, and servicing on medical devices that they have placed on the market; or
c) implantable or single-use medical devices.
Informaciones generales
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Estado: En desarrolloEtapa: Estudio de CD iniciado [30.20]
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Edición: 1
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Comité Técnico :ISO/TC 210
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