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05/30060678 DC : DRAFT SEP 2005

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

BS EN ISO 22794 - DENTISTRY - IMPLANTABLE MATERIALS FOR BONE FILLING AND AUGMENTATION IN ORAL AND MAXILLOFACIAL SURGERY - CONTENTS OF A TECHNICAL FILE

Superseded date

31-08-2007

Superseded by

BS EN ISO 22794:2009

Published date

23-11-2012

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BS EN ISO 22794

Committee
CH/106/8
DocumentType
Draft
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

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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