Resumen
ISO 18113-2:2009 specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents for professional use.
ISO 18113-2:2009 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for professional use.
ISO 18113-2:2009 can also be applied to accessories.
ISO 18113-2:2009 applies to the labels for outer and immediate containers and to the instructions for use.
Informaciones generales
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Estado: RetiradaFecha de publicación: 2009-12Etapa: Retirada de la Norma Internacional [95.99]
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Edición: 1Número de páginas: 10
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Comité Técnico :ISO/TC 212ICS :11.100.10
- RSS actualizaciones
Ciclo de vida
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Ahora
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Revisada por
PublicadoISO 18113-2:2022