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BSI - BS EN ISO 14630

Non-active surgical implants - General requirements

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Organization: BSI
Publication Date: 31 December 2012
Status: active
Page Count: 26
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

BS EN ISO 14630
December 31, 2012
Non-active surgical implants - General requirements
A description is not available for this item.
BS EN ISO 14630
November 30, 2009
Non-active surgical implants - General requirements
A description is not available for this item.
BS EN ISO 14630
December 31, 2008
Non-active surgical implants - General requirements
A description is not available for this item.
BS EN ISO 14630
August 2, 2005
Non-active surgical implants General requirements
A description is not available for this item.
BS EN ISO 14630
January 15, 1998
General Requirements for Non-Active Surgical Implants
This European Standard specifies general requirements for non-active surgical implants. This standard is not applicable to dental implants, dental restorative materials, transendodontic and...

References

This document references:
BS EN ISO 14937 - 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
Published by BSI on March 31, 2010
A description is not available for this item.
This document references:
BS EN ISO 16061 - Instruments for use in association with non-active surgical implants — General requirements
Published by BSI on April 30, 2021
A description is not available for this item.
This document references:
BS EN ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by BSI on September 29, 2006
A description is not available for this item.
This document references:
BS EN ISO 14937 - 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
Published by BSI on March 31, 2010
A description is not available for this item.
This document references:
BS EN ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by BSI on September 29, 2006
A description is not available for this item.
This document references:
BS EN ISO 16061 - Instruments for use in association with non-active surgical implants — General requirements
Published by BSI on April 30, 2021
A description is not available for this item.
This document is referenced by:
BS EN ISO 22794 - Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file
Published by BSI on September 30, 2009
A description is not available for this item.
This document is referenced by:
BS ISO 23317 - Implants for surgery — In vitro evaluation for apatite-forming ability of implant materials
Published by BSI on June 30, 2014
A description is not available for this item.
This document is referenced by:
BS EN ISO 16672 - Ophthalmic implants - Ocular endotamponades
Published by BSI on October 31, 2021
A description is not available for this item.
This document is referenced by:
BS EN ISO 25539-2 - Cardiovascular implants - Endovascular devices Part 2: Vascular stents
Published by BSI on October 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 11979-8 - Ophthalmic implants - Intraocular lenses Part 8: Fundamental requirements
Published by BSI on June 30, 2017
A description is not available for this item.
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