DIN EN ISO 11979-3:2013-04
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OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 3: MECHANICAL PROPERTIES AND TEST METHODS (ISO 11979-3:2012) |
DIN EN ISO 11979-1:2013-01
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OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 1: VOCABULARY (ISO 11979-1:2012) |
ISO 11979-10:2006
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Ophthalmic implants Intraocular lenses Part 10: Phakic intraocular lenses |
DIN EN ISO 11979-9:2014-12
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OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 9: MULTIFOCAL INTRAOCULAR LENSES (ISO 11979-9:2006 + AMD.1:2014) |
ISO 11979-7:2014
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Ophthalmic implants Intraocular lenses Part 7: Clinical investigations |
DIN EN ISO 14971:2013-04
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MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007) |
DIN EN ISO 11979-10:2014-12
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OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 10: PHAKIC INTRAOCULAR LENSES (ISO 11979-10:2006 + AMD.1:2014) |
DIN EN ISO 11979-4:2013-01
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OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 4: LABELLING AND INFORMATION (ISO 11979-4:2008 + AMD.1:2012) |
DIN EN ISO 11979-2:2014-12
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OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 2: OPTICAL PROPERTIES AND TEST METHODS (ISO 11979-2:2014) |
ISO 14630:2012
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Non-active surgical implants General requirements |
DIN EN ISO 11979-5:2010-11
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Ophthalmic implants - Intraocular lenses - Part 5: Biocompatibility (ISO 11979-5:2006) |
ISO 11979-3:2012
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Ophthalmic implants — Intraocular lenses — Part 3: Mechanical properties and test methods |
DIN EN ISO 14630:2013-03
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Non-active surgical implants - General requirements (ISO 14630:2012) |
ISO/TR 22979:2017
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Ophthalmic implants — Intraocular lenses — Guidance on assessment of the need for clinical investigation of intraocular lens design modifications |
ISO 11979-9:2006
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Ophthalmic implants Intraocular lenses Part 9: Multifocal intraocular lenses |
ISO 11979-1:2006
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Ophthalmic implants Intraocular lenses Part 1: Vocabulary |
DIN EN ISO 11979-6:2015-02
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Ophthalmic implants - Intraocular lenses - Part 6: Shelf-life and transport stability testing (ISO 11979-6:2014) |
DIN EN ISO 14155:2012-01
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CLINICAL INVESTIGATION OF MEDICAL DEVICES FOR HUMAN SUBJECTS - GOOD CLINICAL PRACTICE (ISO 14155:2011 + COR. 1:2011) |
ISO 11979-4:2008
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Ophthalmic implants — Intraocular lenses — Part 4: Labelling and information |
DIN EN ISO 11979-7:2014-12
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OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 7: CLINICAL INVESTIGATIONS (ISO 11979-7:2014) |
ISO 14155:2011
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Clinical investigation of medical devices for human subjects Good clinical practice |
ISO 11979-2:2014
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Ophthalmic implants — Intraocular lenses — Part 2: Optical properties and test methods |
ISO 11979-5:2006
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Ophthalmic implants Intraocular lenses Part 5: Biocompatibility |
ISO 14971:2007
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Medical devices Application of risk management to medical devices |
ISO 11979-6:2014
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Ophthalmic implants — Intraocular lenses — Part 6: Shelf-life and transport stability testing |