delSRPS EN ISO 10993-7:2011/prA11:2024

Биолошко вредновање медицинских средстава – Део 7: Остаци после стерилизације етилен-оксидом - Измена 11

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals

Апстракт

This part of ISO 10993 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 this document is applied, are also included in the informative annexes. EO-sterilized devices that have no patient contact (e.g., in vitro diagnostic devices) are not covered by this part of ISO 10993

Повезане директиве

НАПОМЕНА: Уколико се у пољу са називом директиве не налази реч „хармонизован“ (обележена зеленом бојом), то значи да европски стандард није цитиран у OJEU.