DIN EN ISO 11607-2:2014-11
Withdrawn
View Superseded by
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES (ISO 11607-2:2006 + AMD 1.:2014)
Hardcopy , PDF
English
11-01-2014
01-29-2021
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized.
| Committee |
TC 198
|
| DevelopmentNote |
DRAFT 2017 issued in November 2017. (11/2017)
|
| DocumentType |
Standard
|
| Pages |
21
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| I.S. EN ISO 11607-2:2017 & LC:2017 | Identical |
| NS EN ISO 11607-2 : 2017 | Identical |
| BS EN ISO 11607-2 : 2006 | Identical |
| NBN EN ISO 11607-2 : 2006 AMD 1 2014 | Identical |
| ISO 11607-2:2006 | Identical |
| EN ISO 11607-2:2017 | Identical |
| UNE-EN ISO 11607-2:2017 | Identical |
| NF EN ISO 11607-2:2018 | Identical |
| NEN EN ISO 11607-2 : 2017 + COR 2017 | Identical |
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