Comment Closes On
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Committee
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CH/106/8 |
Document Type
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Draft |
ISBN
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Pages
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Published
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Publisher
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British Standards Institution
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Status
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Superseded |
Superseded By
|
|
ISO 11135:2014
|
Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices |
ISO 1942-1:1989
|
Dental vocabulary Part 1: General and clinical terms |
ISO 14937:2009
|
Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
EN 1041:2008+A1:2013
|
Information supplied by the manufacturer of medical devices |
ISO 10993-7:2008
|
Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals |
ISO 10993-17:2002
|
Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances |
ISO 10993-1:2009
|
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 11607:2003
|
Packaging for terminally sterilized medical devices |
ISO 14971-1:1998
|
Medical devices Risk management Part 1: Application of risk analysis |
ISO 14155:2011
|
Clinical investigation of medical devices for human subjects Good clinical practice |
ISO 11134:1994
|
Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization |
ISO 11137:1995
|
Sterilization of health care products Requirements for validation and routine control Radiation sterilization |
ISO 15223:2000
|
Medical devices Symbols to be used with medical device labels, labelling and information to be supplied |
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