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ISO 10993-7:2026

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

Summary

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.

Notes

60.00 : Norme internationale en cours de publication

Technical characteristics

Publisher International Organization for Standardization (ISO)
Publication Date 01/17/2026
Edition 3
Page Count 126
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ISBN ---
Weight (in grams) ---