Resumen
ISO 10993-7:2008 specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices, procedures for the measurement of EO and ECH, and methods for determining compliance so that devices may be released. Additional background, including guidance and a flowchart showing how the standard is applied are also included in informative annexes.
EO-sterilized devices that have no patient contact (e.g., in vitro diagnostic devices) are not covered by ISO 10993-7:2008.
Informaciones generales
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Estado: En desarrolloEtapa: Informe completo distribuido: DIS aprobado para su registro como FDIS [40.99]
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Edición: 3Número de páginas: 118
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Comité Técnico :ISO/TC 194ICS :11.100.20
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Ciclo de vida
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Anteriormente
PublicadoISO 10993-7:2008
PublicadoISO 10993-7:2008/Amd 1:2019
PublicadoISO 10993-7:2008/Cor 1:2009
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Ahora