Resumen
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for professional use.
This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use.
This document can also be applicable to accessories.
This document does not apply to:
a) instructions for instrument servicing or repair;
b) IVD reagents, including calibrators and control materials for use in control of the reagent;
c) IVD instruments for self-testing.
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Informaciones generales
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Estado: PublicadoFecha de publicación: 2022-10Etapa: Norma Internacional publicada [60.60]
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Edición: 2Número de páginas: 10
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Comité Técnico :ISO/TC 212ICS :11.100.10
- RSS actualizaciones
Ciclo de vida
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Anteriormente
RetiradaISO 18113-3:2009
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Ahora
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