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DIN EN ISO 11979-5

Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO 11979-5:2006); German version EN ISO 11979-5:2006

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Organization: DIN
Publication Date: 1 November 2010
Status: active
Page Count: 34
ICS Code (Ophthalmic equipment): 11.040.70

Document History

DIN EN ISO 11979-5
May 1, 2021
Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO 11979-5:2020); German version EN ISO 11979-5:2020
A description is not available for this item.
DIN EN ISO 11979-5
June 1, 2019
Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO/DIS 11979-5:2019); German and English version prEN ISO 11979-5:2019
A description is not available for this item.
DIN EN ISO 11979-5
November 1, 2010
Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO 11979-5:2006); German version EN ISO 11979-5:2006
A description is not available for this item.
DIN EN ISO 11979-5
September 1, 2006
Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO 11979-5:2006); German version EN ISO 11979-5:2006
A description is not available for this item.
DIN EN ISO 11979-5
November 1, 2004
Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO/DIS 11979-5:2004); German version prEN ISO 11979-5:2004
A description is not available for this item.
DIN EN ISO 11979-5
December 1, 1995
Optics and optical instruments - Intraocular lenses - Part 5: Biocompatibility (ISO/DIS 11979-5:1995); German version prEN ISO 11979-5:1995
A description is not available for this item.
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References

This document is referenced by:
DIN EN ISO 11979-10 - Ophthalmische Implantate - Intraokularlinsen - Teil 10: Klinische Pruefungen von Intraokularlinsen zur Korrektion der Ametropie in phaken Augen (ISO 11979-10:2018); Deutsche Fassung EN ISO 11979-10:2018
Published by DIN on August 1, 2018
Dieses Dokument legt Anforderungen für Intraokularlinsen fest, die zur Implantation in den Vorderabschnitt des Auges vorgesehen sind mit der primären Indikation, dessen Brechkraft zu modifizieren. Es...
This document is referenced by:
DIN EN ISO 11979-6 - Ophthalmic implants - Intraocular lenses - Part 6: Shelf-life and transport stability testing (ISO 11979-6:2014); German version EN ISO 11979-6:2014
Published by DIN on February 1, 2015
Dieser Teil von ISO 11979 legt Prüfverfahren fest, mit denen die Haltbarkeit steriler Intraokularlinsen (IOL) in ihrer Endverpackung bestimmt werden kann. Diese Prüfverfahren beinhalten Verfahren zur...
This document is referenced by:
DIN EN ISO 11979-1 - Ophthalmic implants - Intraocular lenses - Part 1: Vocabulary (ISO 11979-1:2018); German version EN ISO 11979-1:2018
Published by DIN on May 1, 2019
A description is not available for this item.
This document is referenced by:
DIN EN ISO 11979-4 - Ophthalmic implants - Intraocular lenses - Part 4: Labelling and information (ISO 11979-4:2008 + Amd.1:2012); German version EN ISO 11979-4:2008 + A1:2012
Published by DIN on January 1, 2013
Dieser Teil von ISO 11979 legt Anforderungen an die Etikettierung von Intraokularlinsen (IOLs) und die in oder auf deren Verpackung anzugebenden Informationen fest. ANMERKUNG Dieser Teil von ISO...
This document is referenced by:
DIN EN ISO 11979-7 - Ophthalmische Implantate - Intraokularlinsen - Teil 7: Klinische Pruefungen von Intraokularlinsen fuer die Korrektion von Aphakie (ISO 11979-7:2018); Deutsche Fassung EN ISO 11979-7:2018
Published by DIN on August 1, 2018
Dieses Dokument legt die besonderen Anforderungen an die klinische Prüfung von Intraokularlinsen (IOL) fest, die zur Korrektur von Aphakie in das Auge implantiert werden.
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