DIN EN ISO 7439:2015-08
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by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 (ISO 7439:2015)
Available format(s)
Hardcopy , PDF
Superseded date
01-07-2023
Superseded by
Language(s)
German, English
Published date
01-08-2015
Important note : Users cannot be edited or removed once added to your Multi user PDF.| DocumentType |
Standard
|
| Pages |
19
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ONORM EN ISO 7439 : 2015 | Identical |
| BS EN ISO 7439:2015 | Identical |
| UNI EN ISO 7439 : 2011 | Identical |
| EN ISO 7439:2015 | Identical |
| I.S. EN ISO 7439:2015 | Identical |
| NBN EN ISO 7439 : 2015 | Identical |
| NEN EN ISO 7439 : 2015 | Identical |
| NS EN ISO 7439 : 2015 | Identical |
| SN EN ISO 7439 : 2015 | Identical |
| UNE-EN ISO 7439:2015 | Identical |
| NF EN ISO 7439 : 2015 | Identical |
| ISO 7439:2015 | Identical |
| DIN EN ISO 15223-1:2015-08 (Draft) | MEDICAL DEVICES - SYMBOLS TO BE USED WITH MEDICAL DEVICE LABELS, LABELLING AND INFORMATION TO BE SUPPLIED - PART 1: GENERAL REQUIREMENTS (ISO 15223-1:2016, CORRECTED VERSION 2017-03) |
| ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects Part 1: General requirements |
| DIN EN ISO 14971:2013-04 | MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007) |
| 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 |
| DIN EN ISO 14155-1:2009-11 | CLINICAL INVESTIGATION OF MEDICAL DEVICES FOR HUMAN SUBJECTS - PART 1: GENERAL REQUIREMENTS |
| DIN EN ISO 14630:2013-03 | Non-active surgical implants - General requirements (ISO 14630:2012) |
| 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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