ISO 7439:2015
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
Copper-bearing contraceptive intrauterine devices — Requirements and tests
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
09-04-2025
French, English
09-02-2015
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 |
Withdrawn
|
| 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 |
Important note : Users cannot be edited or removed once added to your Multi user PDF.Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.
Logging out.