ISO 10993-7:2008 — Biological evaluation — Part 7: Ethylene oxide sterilization residuals

ISO 10993 Series ISO 2008-10-01
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Summary

Specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices, and procedures for measurement of residual EO and ECH. Critical for devices sterilized with ethylene oxide.

Standard Details

This standard is referenced in the harmonized standards lists for the EU Medical Device Regulation (MDR) 2017/745, EU In Vitro Diagnostic Regulation (IVDR) 2017/746, and is recognized by regulatory authorities worldwide including the FDA, Health Canada, and TGA.

Document Details

Document IDISO 10993-7:2008
TypeISO 10993 Series
AuthorityISO
Publication Date2008-10-01

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TypeISO 10993 Series
Published ByISO
Date2008-10-01

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