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ISO 11135-1:2007 PDF

ISO 11135-1:2007 PDF

Name:
ISO 11135-1:2007 PDF

Published Date:
05/01/2007

Status:
[ Withdrawn ]

Description:

Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices

Publisher:
International Organization for Standardization

Document status:
Active
Format:
Electronic (PDF)
Delivery time:
10 minutes
Delivery time (for Russian version):
200 business days
SKU:
Choose Document Language:
$56.7
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Identical versions for sale:
Outside United States: BS EN ISO 11135-1:2007
German: DIN EN ISO 11135-1:2007
Spanish: UNE EN ISO 11135-1:2007

ISO 11135-1:2007 specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.

Sterilization processes validated and controlled in accordance with the requirements of ISO 11135-1:2007 are not assumed to be effective in inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeld Jacob disease. Specific recommendations have been produced in particular countries for the processing of materials potentially contaminated with these agents.


File Size : 1 file , 310 KB
Note : This product is unavailable in Ukraine, Russia, Belarus
Published : 05/01/2007
Same As : ISO 11135-1:2007

History

ISO 11135:2014
ISO 11135:2014
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Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
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ISO 11135-1:2007
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Published Date: 05/01/2007
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
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ISO 11135:1994
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