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Vabandust – see toode pole enam saadaval

prEN ISO 10993-7

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO/DIS 10993-7:2024)

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ISO/DIS 10993-7; prEN ISO 10993-7
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Kuupäev
Tüüp
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Põhitekst
prEN ISO 10993-7
01.02.2022
Muudatus
01.02.2022
Põhitekst + muudatus
06.01.2010
Parandus
09.01.2009
Põhitekst
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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