I.S. EN ISO 11979-4:2008
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
OPHTHALMIC IMPLANTS - INTRAOCULAR LENSES - PART 4: LABELLING AND INFORMATION (ISO 11979-4:2008)
Hardcopy , PDF
English
01-01-2008
10-07-2020
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
Dates of withdrawal of national standards are available from NSAI.
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Information provision
5 Labelling
6 Package insert
7 Self-adhesive label
8 Use of symbols
9 Additional information
Bibliography
Describes the labelling requirements for intraocular lenses (IOLs) and the information to be provided within or on the packaging.
| DocumentType |
Standard
|
| Pages |
20
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ISO 11979-4:2008 | Identical |
| NEN EN ISO 11979-4 : 2009 AMD 1 2012 | Identical |
| DIN EN ISO 11979-4:2013-01 | Identical |
| NS EN ISO 11979-4 : 2008 AMD 1 2012 | Identical |
| NBN EN ISO 11979-4 : 2009 AMD 1 2012 | Identical |
| NF EN ISO 11979-4 : 2009 AMD 1 2012 | Identical |
| BS EN ISO 11979-4 : 2008 | Identical |
| EN ISO 11979-4:2008 | Equivalent |
| UNE-EN ISO 11979-4:2009 | Identical |
| ISO 11607-2:2006 | Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| ISO 11979-1:2006 | Ophthalmic implants — Intraocular lenses — Part 1: Vocabulary |
| 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 |
| EN 980:2008 | Symbols for use in the labelling of medical devices |
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