ISO 11135:1994
Medical devices -- Validation and routine control of ethylene oxide sterilization
This standard has been revised by: ISO 11135-1:2007
Abstract
Establishes requirements and guidance. Particular attention is drawn to the need for specific testing for safety, quality and efficacy, possibly exceeding the general requirements, which may be necessary for a specific product. Attention is drawn to the existence in some countries of regulations laying down safety requirements for handling ethylene oxide and for premises in which it is used as well as of regulations laying down limits for the level of ethylene oxide residues within medical devices and products.
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Edition: 1 (Monolingual) ICS: 11.080.01 Status: Withdrawn Stage: 95.99 (2008-07-17) TC/SC: ISO/TC 198 Number of Pages: -
Revised by: ISO 11135-1:2007
Revised by: ISO/TS 11135-2:2008
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No corrigenda or amendments available


