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ISO 10993-7:2026
Biological evaluation of medical devices
Part 7: Ethylene oxide sterilization residuals
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 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
Replaces
13/10/2008
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Previous versions
17/01/2026
Forthcoming
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13/10/2008
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, Under review
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