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JSA - JIS T 6541

Contents of technical file for dental implant systems

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Organization: JSA
Publication Date: 1 September 2013
Status: active
ICS Code (Dental implants): 11.060.15

Document History

JIS T 6541
September 1, 2013
Contents of technical file for dental implant systems
A description is not available for this item.

References

This document references:
ISO 10993-9 - Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products
Published by ISO on November 1, 2019
This document provides general principles for the systematic evaluation of the potential and observed degradation of medical devices through the design and performance of in vitro degradation...
This document references:
ISO 14405-2 - Geometrical product specifications (GPS) - Dimensional tolerancing - Part 2: Dimensions other than linear or angular sizes
Published by ISO on December 1, 2018
This document illustrates the ambiguity caused by the use of dimensional specifications to control properties other than linear or angular size and the benefit of using geometrical specifications...
This document references:
ISO 14801 - Dentistry - Implants - Dynamic loading test for endosseous dental implants
Published by ISO on November 1, 2016
A description is not available for this item.
This document references:
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 ISO on October 15, 2009
Inclusions This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation and routine monitoring and control of a...
This document references:
ISO 17664 - Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices
Published by ISO on October 1, 2017
This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of a medical device that requires cleaning followed by disinfection...
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