NS EN ISO 11607-2 : 2017
Withdrawn
Withdrawn
PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: VALIDATION REQUIREMENTS FOR FORMING, SEALING AND ASSEMBLY PROCESSES (ISO 11607-2:2006)
Published date
01-12-2013
Withdrawn date
03-01-2020
Sorry this product is not available in your region.
Defines the requirements for development and validation of processes for packaging medical devices that are terminally sterilized.
| DocumentType |
Standard
|
| PublisherName |
Norwegian Standards (Norges Standardiseringsforbund)
|
| Status |
Withdrawn
|
| Standards | Relationship |
| EN ISO 11607-2:2017 | Identical |
| BS EN ISO 11607-2 : 2006 | Identical |
| I.S. EN ISO 11607-2:2017 & LC:2017 | Identical |
| DIN EN ISO 11607-2:2014-11 | Identical |
| NBN EN ISO 11607-2 : 2006 AMD 1 2014 | Identical |
| ISO 11607-2:2006 | Identical |
| UNE-EN ISO 11607-2:2017 | Identical |
| NF EN ISO 11607-2 : 2018 | Identical |
| NEN EN ISO 11607-2 : 2017 + COR 2017 | Identical |
Summarise
Sorry this product is not available in your region.