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DIN EN ISO 10993-7

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)

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Organization: DIN
Publication Date: 1 February 2009
Status: active
Page Count: 98
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

DIN EN ISO 10993-7
September 1, 2022
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008 + Cor 1:2009 + Amd 1:2019)
A description is not available for this item.
DIN EN ISO 10993-7/A1
August 1, 2018
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Amendment 1 (ISO 10993-7:2008/DAM 1:2018); German and English version EN ISO 10993-7:2008/prA1:2018
A description is not available for this item.
DIN EN ISO 10993-7
June 1, 2011
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008); Corrigendum 1 to English translation of DIN EN ISO 10993-7:2009-02
A description is not available for this item.
DIN EN ISO 10993-7
February 1, 2009
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
A description is not available for this item.
DIN EN ISO 10993-7
November 1, 1995
Biological evaluation of medical devices - Ethylene oxide sterilization residuals (ISO 10993-7:1995)
A description is not available for this item.

References

This document is referenced by:
DIN EN ISO 7199 - Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO 7199:2016 + Amd 1:2020) (includes Amendment :2020)
Published by DIN on October 1, 2020
A description is not available for this item.
This document is referenced by:
DIN EN ISO 7198 - Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016)
Published by DIN on July 1, 2017
This International Standard specifies requirements for the evaluation of vascular prostheses and requirements with respect to nomenclature, design attributes and information supplied by the...
This document is referenced by:
DIN EN ISO 15621 - Absorbent incontinence aids for urine and/or faeces - General guidelines on evaluation (ISO 15621:2017)
Published by DIN on September 1, 2017
This document gives guidelines for evaluating absorbent incontinence aids for urine and/or faeces. It provides a context for the procedures described in other International Standards and published...
This document is referenced by:
DIN EN ISO 10993-4 - Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)
Published by DIN on December 1, 2017
This document specifies general requirements for evaluating the interactions of medical devices with blood. It describes a) a classification of medical devices that are intended for use in contact...
This document is referenced by:
DIN EN ISO 16671 - Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2015 + Amd 1:2017) (includes Amendment :2017)
Published by DIN on March 1, 2018
This International Standard defines requirements with regards to safety for the intended performance, design attributes, preclinical and clinical evaluation, sterilization, product packaging, product...
This document is referenced by:
DIN EN ISO 17664 - Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)
Published by DIN on April 1, 2018
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...
This document is referenced by:
DIN EN ISO 8637-2 - Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018)
Published by DIN on December 1, 2018
WARNING — Other requirements and other EU Directives may be applicable to the product(s) falling within the scope of this document. This document specifies requirements for the blood circuit for...
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