ISO 11979-8:2017
Current
The latest, up-to-date edition.
Ophthalmic implants — Intraocular lenses — Part 8: Fundamental requirements
Hardcopy , PDF
English, French
12-04-2017
ISO 11979-8:2017 specifies fundamental requirements for all types of intraocular lenses intended for surgical implantation into the anterior segment of the human eye, excluding corneal implants and transplants.
| Committee |
ISO/TC 172/SC 7
|
| DevelopmentNote |
Supersedes ISO/DIS 11979-8. (04/2017)
|
| DocumentType |
Standard
|
| Pages |
4
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| DIN EN ISO 11979-8:2017-08 | Identical |
| DIN EN ISO 11979-8:2016-04 (Draft) | Identical |
| NEN EN ISO 11979-8 : 2017 | Identical |
| NS EN ISO 11979-8 : 2017 | Identical |
| I.S. EN ISO 11979-8:2017 | Identical |
| PN EN ISO 11979-8 : 2017 | Identical |
| SS-EN ISO 11979-8:2017 | Identical |
| EN ISO 11979-8:2017 | Identical |
| BS EN ISO 11979-8:2017 | Equivalent |
| DIN EN 13503-8:2000-07 | Corresponds |
| UNE-EN 13503-8:2000 | Identical |
| UNE-EN ISO 11979-8:2017 | Identical |
| I.S. EN 13503-8:2000 | Identical |
| BIS IS/ISO 11979-8 : 2006 | Identical |
| BS EN ISO 11979-8:2017 | Identical |
| I.S. EN ISO 11979-10:2007 | OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 10: CLINICAL INVESTIGATIONS OF INTRAOCULAR LENSES FOR CORRECTION OF AMETROPIA IN PHAKIC EYES (ISO 11979-10:2018) |
| EN ISO 11979-10:2018 | Ophthalmic implants - Intraocular lenses - Part 10: Clinical investigations of intraocular lenses for correction of ametropia in phakic eyes (ISO 11979-10:2018) |
| 17/30335550 DC : 0 | BS EN ISO 11979-10 - OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 10: CLINICAL INVESTIGATIONS OF INTRAOCULAR LENSES FOR CORRECTION OF AMETROPIA IN PHAKIC EYES |
| PD ISO/TR 22979:2017 | Ophthalmic implants. Intraocular lenses. Guidance on assessment of the need for clinical investigation of intraocular lens design modifications |
| ISO/TR 22979:2017 | Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications |
| ISO 11979-10:2006 | Ophthalmic implants — Intraocular lenses — Part 10: Phakic intraocular lenses |
| ISO 11979-7:2014 | Ophthalmic implants — Intraocular lenses — Part 7: Clinical investigations |
| ISO 14630:2012 | Non-active surgical implants — General requirements |
| ISO 11979-3:2012 | Ophthalmic implants — Intraocular lenses — Part 3: Mechanical properties and test methods |
| ISO/TR 22979:2017 | Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications |
| ISO 11979-9:2006 | Ophthalmic implants — Intraocular lenses — Part 9: Multifocal intraocular lenses |
| ISO 11979-1:2006 | Ophthalmic implants — Intraocular lenses — Part 1: Vocabulary |
| ISO 11979-4:2008 | Ophthalmic implants — Intraocular lenses — Part 4: Labelling and information |
| ISO 14155:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice |
| ISO 11979-2:2014 | Ophthalmic implants — Intraocular lenses — Part 2: Optical properties and test methods |
| ISO 11979-5:2006 | Ophthalmic implants — Intraocular lenses — Part 5: Biocompatibility |
| ISO 14971:2007 | Medical devices — Application of risk management to medical devices |
| ISO 11979-6:2014 | Ophthalmic implants — Intraocular lenses — Part 6: Shelf-life and transport stability testing |
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