DIN EN ISO 11607-1:2014-11
Withdrawn
View Superseded by
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 1: REQUIREMENTS FOR MATERIALS, STERILE BARRIER SYSTEMS AND PACKAGING SYSTEMS (ISO 11607-1:2006 + AMD 1.:2014)
Hardcopy , PDF
11-01-2014
01-29-2021
This part of ISO 11607 specifies 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.
| Committee |
TC 198
|
| DevelopmentNote |
Supersedes DIN EN 868-1. (07/2006) DRAFT 2017 issued in November 2017. (11/2017)
|
| DocumentType |
Test Method
|
| Pages |
42
|
| ProductNote |
NEW CHILD COR 1 2016 IS NOW ADDED
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ISO 11607-1:2006 | Identical |
| NS EN ISO 11607-1 : 2017 | Identical |
| BS EN ISO 11607-1 : 2009 | Identical |
| NBN EN ISO 11607-1 : 2009 + A1 2014 | 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 |
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