SN EN ISO 14602:2012
Current
The latest, up-to-date edition.
NON-ACTIVE SURGICAL IMPLANTS - IMPLANTS FOR OSTEOSYNTHESIS - PARTICULAR REQUIREMENTS (ISO 14602:2010)
Hardcopy
01-01-2012
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Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
4 Intended performance
5 Design attributes
6 Materials
7 Design evaluation
8 Manufacturing
9 Sterilization
10 Packaging
11 Information supplied by the manufacturer
Annex A (informative) ISO Standards referring to implants and
associated instruments found acceptable through clinical use
for given applications in osteosynthesis
Annex B (informative) ISO standards referring to materials
found acceptable through proven clinical use
Annex C (informative) Standards relating to testing and
design evaluation
Annex ZA (informative) Clauses of this European Standard
addressing essential requirements or other provisions of
EU Directives
Defines particular requirements for non-active surgical implants for osteosynthesis. Supplies particular requirements for intended performance, design attributes, materials, design evaluation, manufacturing, sterilization, packaging and information supplied by the manufacturer.
| Committee |
INB/NK 129
|
| DocumentType |
Standard
|
| Pages |
0
|
| PublisherName |
Swiss Standards
|
| Status |
Current
|
| Standards | Relationship |
| NBN EN ISO 14602 : 2011 | Identical |
| EN ISO 14602:2011 | Identical |
| BS EN ISO 14602:2011 | Identical |
| NEN EN ISO 14602 : 2012 | Identical |
| NS EN ISO 14602 : 2011 | Identical |
| UNE-EN ISO 14602:2012 | Identical |
| DIN EN ISO 14602:2012-06 | Identical |
| ISO 14602:2010 | Identical |
| NF EN ISO 14602 : 2012 | Identical |
| I.S. EN ISO 14602:2011 | Identical |
| UNI EN ISO 14602 : 2012 | Identical |
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