UNLIMITED FREE ACCESS TO THE WORLD'S BEST IDEAS

close
Standards Library
  • All
  • News & Analysis
  • Products & Services
  • Standards Library
  • Reference Library
  • Community

I forgot my password.

Don't have an account?

Register here.

BSI - BS EN ISO 16672

Ophthalmic implants - Ocular endotamponades

active, Most Current
Buy Now
Organization: BSI
Publication Date: 31 August 2015
Status: active
Page Count: 26
ICS Code (Ophthalmic equipment): 11.040.70

Document History

18/30345295 DC
August 9, 2018
Draft BS EN ISO 16672 Ophthalmic implants — Ocular endotamponades.
A description is not available for this item.
BS EN ISO 16672
August 31, 2015
Ophthalmic implants - Ocular endotamponades
A description is not available for this item.
BS EN ISO 16672
August 31, 2015
Ophthalmic implants - Ocular endotamponades
A description is not available for this item.
BS EN ISO 16672
May 1, 2003
Ophthalmic implants - Ocular endotamponades
A description is not available for this item.

References

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 14630 FRENCH - Implants chirurgicaux non actifs - Exigences générales
Published by ISO on December 1, 2012
A description is not available for this item.
This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
ISO 10993-6 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 6: Essais concernant les effets locaux après implantation
Published by ISO on December 1, 2016
A description is not available for this item.
This document references:
ISO 11135 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices AMENDMENT 1: Revision of Annex E, Single batch release
Published by ISO on October 1, 2018
A description is not available for this item.
View Less
View All
Advertisement