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BS EN ISO 16672:2015

Withdrawn

Withdrawn

View Superseded by

Ophthalmic implants. Ocular endotamponades

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

06-30-2017

Withdrawn date

10-31-2021

Superseded by

BS EN ISO 16672:2021

US$341.23
Excluding Tax where applicable

Committee
CH/172/7
DevelopmentNote
Supersedes 01/561619 DC (05/2003) Supersedes 14/30295064 DC. (09/2015)
DocumentType
Standard
Pages
24
PublisherName
British Standards Institution
Status
Withdrawn
SupersededBy
Supersedes

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ISO 14630:2012 Non-active surgical implants — General requirements
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ISO 13408-1:2008 Aseptic processing of health care products — Part 1: General requirements
ISO 20857:2010 Sterilization of health care products — Dry heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 10993-1:2009 Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
ISO 14155:2011 Clinical investigation of medical devices for human subjects — Good clinical practice
ISO 14971:2007 Medical devices — Application of risk management to medical devices
ISO 11607-1:2006 Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems
ISO 15223-1:2016 Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied — Part 1: General requirements
ISO 10993-6:2016 Biological evaluation of medical devices — Part 6: Tests for local effects after implantation
ISO 17665-1:2006 Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices

US$341.23
Excluding Tax where applicable