ISO 7439:2015
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Copper-bearing contraceptive intrauterine devices — Requirements and tests
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
04-04-2023
French, English
02-09-2015
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ISO 7439:2015 specifies requirements and tests for single-use, copper-bearing contraceptive intrauterine devices (IUDs) and their insertion instruments.
It is not applicable to IUDs consisting only of a plastics body or whose primary purpose is to release progestogens.
| Committee |
ISO/TC 157
|
| DevelopmentNote |
Supersedes ISO/FDIS 7439. (02/2015)
|
| DocumentType |
Standard
|
| Pages |
11
|
| PublisherName |
International Organization for Standardization
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| DS EN ISO 7439 : 2015 | Identical |
| ONORM EN ISO 7439 : 2015 | Identical |
| NBN EN ISO 7439 : 2015 | Identical |
| NEN EN ISO 7439 : 2015 | Identical |
| NS EN ISO 7439 : 2015 | Identical |
| I.S. EN ISO 7439:2015 | Identical |
| PN EN ISO 7439 : 2015 | Identical |
| SN EN ISO 7439 : 2015 | Identical |
| UNI EN ISO 7439 : 2011 | Identical |
| SS-EN ISO 7439 : 2015 | Identical |
| UNI EN ISO 7439 : 2015 | Identical |
| UNE-EN ISO 7439:2015 | Identical |
| BS EN ISO 7439:2015 | Identical |
| EN ISO 7439:2015 | Identical |
| NF EN ISO 7439 : 2015 | Identical |
| DIN EN ISO 7439:2015-08 | Identical |
| ABNT NBR ISO 7439:2018 | Identical |
| NFS 90 031 : 1985 | Similar to |
| NBR ISO 7439 : 2014 | Identical |
| ISO 11249:2018 | Copper-bearing intrauterine contraceptive devices — Guidance on the design, execution, analysis and interpretation of clinical studies |
| 14/30302761 DC : 0 | BS ISO 11249 - MECHANICAL CONTRACEPTIVES - GUIDANCE FOR CLINICAL EVALUATION OF INTRA-UTERINE CONTRACEPTIVE DEVICES (IUDS) |
| ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects Part 1: General requirements |
| ISO 14630:2012 | Non-active surgical implants — General requirements |
| EN 12011 : 1998 | INSTRUMENTATION TO BE USED IN ASSOCIATION WITH NON-ACTIVE SURGICAL IMPLANTS - GENERAL REQUIREMENTS |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| ISO 14971:2007 | Medical devices Application of risk management to medical devices |
| ISO 15223-1:2016 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
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