Resumen
ISO/TS 20993:2006 describes a process by which a manufacturer can identify the biological hazards associated with medical devices, estimate and evaluate the risks, control these risks and monitor the effectiveness of the control.
Informaciones generales
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Estado: RetiradaFecha de publicación: 2006-08Etapa: Retirada de la Norma Internacional [95.99]
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Edición: 1Número de páginas: 4
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Comité Técnico :ISO/TC 194ICS :11.100.20
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