DS/EN ISO 10993-7
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization rediduals
inactive
| Organization: | DS |
| Publication Date: | 17 January 1996 |
| Status: | inactive |
| Page Count: | 52 |
| ICS Code (Biological evaluation of medical devices): | 11.100.20 |
scope:
This part of the standard specifies allowable limits for residual limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in ethylene oxide-sterilized medical devices.
Document History
January 17, 2022
Biological evaluation of medical devices – Part 7: Ethylene oxide sterilization residuals – Amendment 1: Applicability of allowable limits for neonates and infants (ISO 10993-7:2008/Amd 1:2019)
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...
November 30, 2009
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals
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...
December 15, 2008
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals
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...
DS/EN ISO 10993-7
January 17, 1996
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization rediduals
This part of the standard specifies allowable limits for residual limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in ethylene oxide-sterilized medical devices.
Biological evaluation of medical devices – Part 7: Ethylene oxide sterilization residuals – Amendment 1 (ISO 10993-7/FDAM 1:2019)
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...
Biological evaluation of medical devices – Part 7: Ethylene oxide sterilization residuals – Amendment 1 (ISO 10993-7/DAM 1:2018)
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...
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/FDIS 10993-7:2008)
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...
Related Products
Searching for related products...