ISO 10993-7:2008
International Standard
Current Edition
·
Approved on
13 October 2008
Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals
ISO 10993-7:2008 Files
English
86 Pages
Current Edition
106.51 OMR
ISO 10993-7:2008 Scope
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.
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