Resumen
ISO 10993-11:2017 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
Informaciones generales
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Estado: En desarrolloEtapa: Estudio de CD iniciado [30.20]
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Edición: 4
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Comité Técnico :ISO/TC 194
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Ciclo de vida
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Anteriormente
PublicadoISO 10993-11:2017
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Ahora
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