ISO 10993-7:2008
$55.25
Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals
Published By | Publication Date | Number of Pages |
ISO | 2008-10 | 94 |
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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.
Published Code | ISO |
---|---|
Published By | International Organization for Standardization |
Publication Date | 2008-10 |
Pages Count | 94 |
Language | France |
Edition | 2 |
File Size | 1.9 MB |
ICS Codes | 11.100.20 - Biological evaluation of medical devices |
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