NS EN ISO 11607-1 : 2017
Withdrawn
Withdrawn
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS (ISO 11607-1:2006)
Published date
01-12-2013
Withdrawn date
03-01-2020
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Defines the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical devices until the point of use.
| DevelopmentNote |
Supersedes NS EN 868-1. (08/2006)
|
| DocumentType |
Standard
|
| PublisherName |
Norwegian Standards (Norges Standardiseringsforbund)
|
| Status |
Withdrawn
|
| Standards | Relationship |
| ISO 11607-1:2006 | Identical |
| BS EN ISO 11607-1 : 2009 | Identical |
| NBN EN ISO 11607-1 : 2009 + A1 2014 | Identical |
| EN ISO 11607-1:2017 | Identical |
| DIN EN ISO 11607-1:2014-11 | Identical |
| NF EN ISO 11607-1:2018 | Identical |
| UNE-EN ISO 11607-1:2017 | Identical |
| I.S. EN ISO 11607-1:2017 | Identical |
| NEN EN ISO 11607-1 : 2017 + COR 2017 | Identical |
Summarise
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