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DIN EN ISO 16671

Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2015 + Amd 1:2017); German version EN ISO 16671:2015 + A1:2017

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Organization: DIN
Publication Date: 1 March 2018
Status: active
Page Count: 36
ICS Code (Ophthalmic equipment): 11.040.70
scope:

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Document History

DIN EN ISO 16671
March 1, 2018
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2015 + Amd 1:2017); German version EN ISO 16671:2015 + A1:2017
.
DIN EN ISO 16671/A1
April 1, 2017
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2015/DAM 1:2017); German and English version EN ISO 16671:2015/prA1:2017
A description is not available for this item.
DIN EN ISO 16671
December 1, 2015
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2015); German version EN ISO 16671:2015
Mit Bezug auf die Sicherheit legt diese Internationale Norm Anforderungen für die beabsichtigte Funktion, Konstruktionsmerkmale, präklinische und klinische Bewertungen, Sterilisation, Verpackung,...
DIN EN ISO 16671
May 1, 2014
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO/DIS 16671:2014); German version prEN ISO 16671:2014
Mit Bezug auf die Sicherheit legt diese Internationale Norm Anforderungen für die beabsichtigte Funktion, Konstruktionsmerkmale, präklinische und klinische Auswertungen, Sterilisation, Verpackung,...
DIN EN ISO 16671
July 1, 2004
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2003); German version EN ISO 16671:2003
A description is not available for this item.
DIN EN ISO 16671
April 1, 2002
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO/DIS 16671:2002); German version prEN ISO 16671:2002
A description is not available for this item.
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References

This document references:
TIR19 AMD 1 - Guidance for ANSI/AAMI/ISO 10993-7:1995, Biological evaluation of medical deices—Part 7: Ethylene oxide sterilization residuals Amendment
Published by AAMI on January 1, 1999
A description is not available for this item.
This document references:
DIN EN 1041 - Information supplied by the manufacturer of medical devices; German version EN 1041:2008+A1:2013
Published by DIN on December 1, 2013
Die vorliegende Europäische Norm legt Anforderungen an Informationen fest, die von einem Hersteller für Medizinprodukte nach der EU-Richtlinie 90/385/EWG zu aktiven implantierbaren medizinischen...
This document references:
DIN EN ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009); German version EN ISO 10993-1:2009
Published by DIN on April 1, 2010
A description is not available for this item.
This document references:
DIN EN ISO 10993-2 - Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006); German version EN ISO 10993-2:2006
Published by DIN on October 1, 2006
A description is not available for this item.
This document references:
DIN EN ISO 10993-6 - Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016); German version EN ISO 10993-6:2016
Published by DIN on September 1, 2017
A description is not available for this item.
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