Abstract
ISO 11137-2:2006 specifies methods of determining the minimum dose needed to achieve a specified requirement for sterility and methods to substantiate the use of 25 kGy or 15 kGy as the sterilization dose to achieve a sterility assurance level (SAL) of 10-6. It also specifies methods of dose auditing in order to demonstrate the continued effectiveness of the sterilization dose.
ISO 11137-2:2006 defines product families for dose establishment and dose auditing.
General information
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Status: WithdrawnPublication date: 2006-04
Corrected version (en): 2006-07
Corrected version (fr): 2006-07Stage: Withdrawal of International Standard [95.99] -
Edition: 1Number of pages: 60
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Technical Committee :ISO/TC 198ICS :11.080.01
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Life cycle
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Previously
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Now
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00
Preliminary
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10
Proposal
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20
Preparatory
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30
Committee
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40
Enquiry
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50
Approval
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60
Publication
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90
Review
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95
Withdrawal
Corrigenda
Correct the current edition; free; not included in the text of the existing standard.WithdrawnISO 11137-2:2006/Cor 1:2009
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00
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Revised by
WithdrawnISO 11137-2:2012