UNE-EN ISO 16671:2016
Current
Current
The latest, up-to-date edition.
Ophthalmic implants - Irrigating solutions for ophthalmic surgery (ISO 16671:2015)
Amended by
Available format(s)
Hardcopy , PDF
Published date
20-01-2016
Publisher
Important note : All end users must be registered with an Account prior to user licenses being assigned.| Committee |
CTN 91
|
| DocumentType |
Standard
|
| Pages |
32
|
| ProductNote |
NEW CHILD AMD 1 IS ADDED NOW
|
| PublisherName |
Asociacion Espanola de Normalizacion
|
| Status |
Current
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| BS EN ISO 16671 : 2015 | Identical |
| DIN EN ISO 16671:2015-12 | Identical |
| NBN EN ISO 16671 : 2015 | Identical |
| ISO 16671:2015 | Identical |
| I.S. EN ISO 16671:2015 | Identical |
| UNI EN ISO 16671 : 2004 | Identical |
| EN ISO 16671:2015 | Identical |
| SN EN ISO 16671 : 2016 AMD 1 2018 | Identical |
| NEN EN ISO 16671 : 2015 AMD 1 2017 | Identical |
| ONORM EN ISO 16671 : 2018 | Identical |
| NS EN ISO 16671 : 2015 AMD 1 2017 | Identical |
| NF EN ISO 16671 : 2015 AMD 1 2018 | Identical |
| AAMI TIR19 : 1998 | GUIDANCE FOR ANSI/AAMI/ISO 10993-7: 1995, BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 7: ETHYLENE OXIDE STERILIZATION RESIDUALS |
| EN ISO 10993-2:2006 | Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) |
| EN ISO 13408-1:2015 | Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) |
| ISO 10993-2:2006 | Biological evaluation of medical devices — Part 2: Animal welfare requirements |
| ISO 22442-1:2015 | Medical devices utilizing animal tissues and their derivatives Part 1: Application of risk management |
| ISO 14630:2012 | Non-active surgical implants — General requirements |
| EN ISO 22442-1:2015 | Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015) |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| ISO 13408-1:2008 | Aseptic processing of health care products — Part 1: General requirements |
| ISO 10993-7:2008 | Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| EN ISO 14971:2012 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) |
| 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 |
| EN ISO 14630:2012 | Non-active surgical implants - General requirements (ISO 14630:2012) |
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