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DIN EN ISO 15798

Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2013 + Amd.1:2017); Deutsche Fassung EN ISO 15798:2013 + A1:2017

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Organization: DIN
Publication Date: 1 February 2018
Status: active
Page Count: 33
ICS Code (Ophthalmic equipment): 11.040.70

Document History

DIN EN ISO 15798
May 1, 2022
Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2022); Deutsche Fassung EN ISO 15798:2022
A description is not available for this item.
DIN EN ISO 15798
February 1, 2021
Ophthalmische Implantante - Viskoelastische Substanzen (ISO/DIS 15798:2020); Deutsche und Englische Fassung prEN ISO 15798:2020
A description is not available for this item.
DIN EN ISO 15798
February 1, 2018
Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2013 + Amd.1:2017); Deutsche Fassung EN ISO 15798:2013 + A1:2017
A description is not available for this item.
DIN EN ISO 15798/A1
April 1, 2016
Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2013/DAM 1:2016), Deutsche und Englische Fassung EN ISO 15798:2013/prA1:2016
A description is not available for this item.
DIN EN ISO 15798
February 1, 2014
Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2013); Deutsche Fassung EN ISO 15798:2013
Diese Internationale Norm ist anwendbar auf ophthalmische viskoelastische Substanzen, einer Klasse nichtaktiver chirurgischer Implantate mit viskosen und/oder viskoelastischen Eigenschaften, die für...
DIN EN ISO 15798
July 1, 2012
Ophthalmische Implantate - Viskoelastische Substanzen (ISO/FDIS 15798:2012); Deutsche Fassung FprEN ISO 15798:2012
A description is not available for this item.
DIN EN ISO 15798
June 1, 2010
Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2010); Deutsche Fassung EN ISO 15798:2010
A description is not available for this item.
DIN EN ISO 15798
August 1, 2008
Ophthalmische Implantate - Viskoelastische Substanzen (ISO/DIS 15798:2008); Deutsche Fassung prEN ISO 15798:2008
A description is not available for this item.
DIN EN ISO 15798 Berichtigung 1
July 1, 2005
Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2001); Deutsche Fassung EN ISO 15798:2001, Berichtigungen zu DIN EN ISO 15798:2001-12; Deutsche Fassung EN ISO 15798:2001/AC:2005
A description is not available for this item.
DIN EN ISO 15798
December 1, 2001
Ophthalmische Implantate - Viskoelastische Substanzen (ISO 15798:2001); Deutsche Fassung EN ISO 15798:2001
A description is not available for this item.
DIN EN ISO 15798
June 1, 2000
Ophthalmische Implantate - Viskoelastische Substanzen (ISO/DIS 15798:2000); Deutsche Fassung prEN ISO 15798:2000
A description is not available for this item.
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References

This document references:
ISO 10993-16 - Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables
Published by ISO on May 1, 2017
This document provides principles on designing and performing toxicokinetic studies relevant to medical devices. Annex A describes the considerations for inclusion of toxicokinetic studies in the...
This document references:
ISO 10993-6 - Biological evaluation of medical devices - Part 6: Tests for local effects after implantation
Published by ISO on December 1, 2016
This part of ISO 10993 specifies test methods for the assessment of the local effects after implantation of biomaterials intended for use in medical devices. This part of ISO 10993 applies to...
This document references:
ISO 11137-3 - Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control
Published by ISO on June 1, 2017
This document gives guidance on meeting the requirements in ISO 11137-1 and ISO 11137-2 and in ISO/TS 13004 relating to dosimetry and its use in development, validation and routine control of a...
This document references:
ISO 22442-2 - Medical devices utilizing animal tissues and their derivatives — Part 2: Controls on sourcing, collection and handling
Published by ISO on September 1, 2020
This document specifies requirements for controls on the sourcing, collection, and handling (which includes storage and transport) of animals and tissues for the manufacture of medical devices...
This document references:
ISO 10993-2 - Biological evaluation of medical devices Part 2: Animal welfare requirements
Published by ISO on July 15, 2006
This part of ISO 10993 is aimed at those who commission, design and perform tests or evaluate data from animal tests undertaken to assess the biocompatibility of materials intended for use in medical...
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